GlyCosmos Portal

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GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	July 8, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

Displaying entries **951 - 975** of **1582** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▼	Disease Ontology
1635	dCMP deaminase	DCTD	Homo sapiens (human)	breast cancer cancer esophagus squamous cell carcinoma gliosarcoma high grade glioma leukopenia mixed glioma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma
3038	hyaluronan synthase 3	HAS3	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Pick's disease Reye syndrome adenocarcinoma adenoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atopic dermatitis basal cell carcinoma bone osteosarcoma cancer carcinoma cardiomyopathy cerebral degeneration childhood osteosarcoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary artery disease cribriform carcinoma dermatitis diabetes mellitus endomyocardial fibrosis esophagus squamous cell carcinoma gallbladder disease gingival fibromatosis glomerulonephritis granular cell carcinoma hepatitis A hepatitis hepatocellular carcinoma hypertrophic cardiomyopathy kidney disease large intestine cancer liver cancer liver disease lung cancer lung non-small cell carcinoma melanoma nephritis nephrosis neuroblastoma osteosarcoma polycystic ovary syndrome primary pulmonary hypertension prostate cancer prostate carcinoma pulmonary hypertension pyoureter rheumatoid arthritis sarcomatoid carcinoma skin melanoma steatotic liver disease transitional cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus
4241	melanotransferrin	MELTF Aliases: CD228 FLJ38863 MAP97 MGC4856 MTF1 MTf melanotransferrin membrane-bound transferrin-like protein	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease MHC class II deficiency Pick's disease Reye syndrome Roberts syndrome Zollinger-Ellison syndrome adenosine deaminase deficiency angiomyolipoma astigmatism bone osteosarcoma cancer carcinoma central nervous system cancer cerebral degeneration cerebral primitive neuroectodermal tumor cervical cancer cervix carcinoma childhood osteosarcoma colorectal cancer colorectal carcinoma dysplastic nevus syndrome embryoma gliosarcoma high grade glioma hyperinsulinism large intestine cancer lung adenocarcinoma lung cancer medulloblastoma medulloepithelioma melanoma melanotic neuroectodermal tumor mixed glioma neuroectodermal tumor obsolete SC phocomelia syndrome obsolete embryonal Tumor with Multilayered Rosettes, C19MC-Altered osteosarcoma polycystic ovary syndrome sarcomatoid carcinoma severe combined immunodeficiency skin melanoma stomach cancer stomach carcinoma supratentorial primitive neuroectodermal tumor
8702	beta-1,4-galactosyltransferase 4	B4GALT4 Aliases: beta4Gal-T4	Homo sapiens (human)	prostate cancer prostate carcinoma
27349	malonyl-CoA-acyl carrier protein transacylase	MCAT Aliases: FASN2C MCT MCT1 MT NET62 [acyl-carrier-protein] S-malonyltransferase fabD	Homo sapiens (human)	B-cell lymphoma Barrett's esophagus Burkitt lymphoma Langerhans-cell histiocytosis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Richter's syndrome abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 actinic keratosis acute myeloid leukemia adenocarcinoma adenoma adult lymphoma benign mastocytoma bladder carcinoma bone osteosarcoma borderline personality disorder brain disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy central nervous system lymphoma cervical adenocarcinoma cervical cancer cervix carcinoma childhood lymphoma childhood osteosarcoma choriocarcinoma chromophobe renal cell carcinoma chronic lymphocytic leukemia clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma congestive heart failure cribriform carcinoma depressive disorder diabetes mellitus diffuse large B-cell lymphoma distal arthrogryposis dysthymic disorder embryoma endomyocardial fibrosis epilepsy esophagus adenocarcinoma esophagus squamous cell carcinoma essential hypertension extracutaneous mastocytoma exudative vitreoretinopathy 1 exudative vitreoretinopathy familial hyperinsulinemic hypoglycemia 1 familial hyperinsulinemic hypoglycemia 2 familial medullary thyroid carcinoma follicular lymphoma gastrointestinal stromal tumor gestational diabetes giant cell glioblastoma glioblastoma granular cell carcinoma hepatocellular carcinoma high grade glioma hyperglycemia hyperinsulinemic hypoglycemia hypertension hypertrophic cardiomyopathy idiopathic generalized epilepsy inflammatory bowel disease insulinoma intermittent explosive disorder invasive ductal carcinoma large intestine cancer liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma major depressive disorder malaria malignant pleural mesothelioma mast cell neoplasm mastocytosis melancholic depression melanoma microphthalmia multiple endocrine neoplasia type 2A multiple myeloma neuroblastoma neurotic disorder non-Hodgkin lymphoma nonpapillary renal cell carcinoma obesity obsolete Matthew-Wood syndrome obsolete melancholia obsolete ymphosarcoma optic atrophy osteomalacia osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary renal cell carcinoma placenta cancer premenstrual tension primary hyperparathyroidism primary pulmonary hypertension prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma reticulosarcoma retinopathy of prematurity rickets sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia skin melanoma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma thyroid gland medullary carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus urinary bladder cancer urticaria pigmentosa visual epilepsy
5288	phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma	PIK3C2G	Homo sapiens (human)	acute myocardial infarction cancer coronary thrombosis diabetes mellitus embryoma familial hyperlipidemia myocardial infarction neuroblastoma progressive supranuclear palsy silent myocardial infarction type 2 diabetes mellitus
81562	lectin, mannose binding 2 like	LMAN2L Aliases: DKFZp564L2423 VIP36-like VIPL	Homo sapiens (human)	agnosia attention deficit hyperactivity disorder autosomal dominant intellectual developmental disorder autosomal recessive intellectual developmental disorder 52 bipolar disorder borderline personality disorder cerebral degeneration choreatic disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma depressive disorder developmental coordination disorder dysthymic disorder dystonia epilepsy focal epilepsy intermittent explosive disorder lingual-facial-buccal dyskinesia major depressive disorder melancholic depression microcephaly neurotic disorder nonpapillary renal cell carcinoma obsolete infantile epileptic encephalopathy obsolete melancholia papillary adenocarcinoma papillary renal cell carcinoma partial motor epilepsy pulmonary emphysema renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 thyroid gland papillary carcinoma visual epilepsy
673	B-Raf proto-oncogene, serine/threonine kinase	BRAF	Homo sapiens (human)	Langerhans-cell histiocytosis Noonan syndrome 7 Noonan syndrome with multiple lentigines 3 bile duct adenoma cancer cardiofaciocutaneous syndrome 1 cardiofaciocutaneous syndrome cardiomyopathy cholangiocarcinoma colon carcinoma colorectal adenocarcinoma colorectal cancer dysembryoplastic neuroepithelial tumor endometrial carcinoma familial melanoma germinoma high grade glioma intrahepatic cholangiocarcinoma lung cancer malignant astrocytoma melanoma pancreatic acinar cell adenocarcinoma pancreatic cancer pleomorphic xanthoastrocytoma prostate adenocarcinoma thyroid gland papillary carcinoma
5230	phosphoglycerate kinase 1	PGK1	Homo sapiens (human)	Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Gilbert syndrome Kawasaki disease Menkes disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Wiskott-Aldrich syndrome X-linked cleft palate with or without ankyloglossia X-linked distal spinal muscular atrophy 3 X-linked dystonia-parkinsonism X-linked severe combined immunodeficiency adenosquamous carcinoma agenesis of the corpus callosum with peripheral neuropathy amyotrophic lateral sclerosis anaplastic astrocytoma anemia ankyloblepharon-ectodermal defects-cleft lip/palate syndrome bilirubin metabolic disorder blindness brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy central nervous system cancer childhood cerebral astrocytoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma combined T cell and B cell immunodeficiency congestive heart failure cystinuria embryoma endometrial adenocarcinoma endometrial cancer endometrial carcinoma endomyocardial fibrosis epilepsy esophageal cancer esophageal carcinoma essential thrombocythemia familial periodic paralysis fibrillary astrocytoma fundus dystrophy galactosemia gallbladder cancer gallbladder carcinoma gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hemolytic anemia hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 hereditary spherocytosis high grade glioma hypertrophic cardiomyopathy hypohidrotic ectodermal dysplasia intellectual disability juvenile pilocytic astrocytoma kidney failure large intestine cancer learning disability liver cancer liver carcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus erythematosus macrocytic anemia malignant astrocytoma melanoma microphthalmia migraine mixed glioma motor peripheral neuropathy myelodysplastic syndrome myoglobinuria myopathy neuroblastoma nonpapillary renal cell carcinoma obsolete Matthew-Wood syndrome obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum occipital horn syndrome ovarian cancer ovarian carcinoma oxyphilic adenoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary adenocarcinoma papillary renal cell carcinoma phosphoglycerate kinase 1 deficiency pilocytic astrocytoma progressive muscular atrophy prostate cancer prostate carcinoma protoplasmic astrocytoma pseudosarcomatous fibromatosis pulmonary large cell neuroendocrine carcinoma pure red-cell aplasia renal carcinoma renal cell carcinoma retinitis pigmentosa 10 rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia skin melanoma spinal muscular atrophy stomach cancer stomach carcinoma subependymal giant cell astrocytoma systemic lupus erythematosus thyroid gland papillary carcinoma uterine corpus cancer visual epilepsy
10678	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	B3GNT2 Aliases: B3GN-T1 B3GN-T2 B3GNT-2 BETA3GNT	Homo sapiens (human)	Graves' disease Walker-Warburg syndrome acute myocardial infarction cancer congenital muscular dystrophy-dystroglycanopathy type A1 coronary thrombosis hyperthyroidism myocardial infarction parapsoriasis prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole schizophrenia silent myocardial infarction thyrotoxicosis transitional cell carcinoma
8867	synaptojanin 1	SYNJ1 Aliases: INPP5G PARK20 inositol polyphosphate-5-phosphatase G phosphoinositide 5-phosphatase synaptic inositol 1,4,5-trisphosphate 5-phosphatase 1	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Creutzfeldt-Jakob disease Down syndrome Duchenne muscular dystrophy Joubert syndrome 1 Joubert syndrome Laron syndrome Parkinson's disease 19A Parkinson's disease 1 Parkinson's disease 20 Parkinson's disease 23 Parkinson's disease 2 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Unverricht-Lundborg syndrome achondroplasia amnestic disorder amyotrophic lateral sclerosis anodontia attention deficit hyperactivity disorder autistic disorder autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy bipolar disorder blepharospasm blindness borderline personality disorder brain disease cerebral degeneration cone-rod dystrophy congenital muscular dystrophy congenital nystagmus congenital ptosis dementia developmental and epileptic encephalopathy 1 developmental and epileptic encephalopathy 53 dissociated nystagmus distal myopathy dystonia early infantile epileptic encephalopathy early myoclonic encephalopathy early-onset Parkinson's disease epilepsy esophagitis facioscapulohumeral muscular dystrophy focal hand dystonia fundus albipunctatus gastroesophageal reflux disease giant cell glioblastoma glioblastoma high grade glioma intellectual disability intermittent explosive disorder isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia locked-in syndrome microcephaly muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 neuroblastoma neurodegenerative disease obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete infantile epileptic encephalopathy oculopharyngeal muscular dystrophy optic atrophy pathologic nystagmus peptic esophagitis progressive muscular atrophy ptosis quadriplegia retinal degeneration retinitis pigmentosa retrograde amnesia rhabdomyosarcoma rippling muscle disease 2 scoliosis secondary Parkinson disease spontaneous ocular nystagmus status epilepticus tauopathy tooth agenesis visual epilepsy
259230	sphingomyelin synthase 1	SGMS1 Aliases: MGC17342 MOB SMS1 phosphatidylcholine:ceramide cholinephosphotransferase 1	Homo sapiens (human)	St. Louis encephalitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis bronchus cancer bronchus carcinoma cancer central nervous system cancer cholangiocarcinoma colorectal cancer colorectal carcinoma diabetes mellitus embryoma giant cell glioblastoma glioblastoma gliosarcoma hepatitis A hepatitis high grade glioma intrahepatic cholangiocarcinoma large intestine cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus erythematosus melanoma mixed glioma pancreatic cancer pancreatic carcinoma pulmonary edema skin melanoma systemic lupus erythematosus type 2 diabetes mellitus
3295	hydroxysteroid 17-beta dehydrogenase 4	HSD17B4 Aliases: 17-beta-HSD IV 17-beta-hydroxysteroid dehydrogenase 4 17beta-estradiol dehydrogenase type IV 3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholest-24-enoyl-CoA hydratase D-3-hydroxyacyl-CoA dehydratase D-bifunctional protein, peroxisomal DBP MFE-2 SDR8C1 beta-hydroxyacyl dehydrogenase beta-keto-reductase peroxisomal multifunctional protein 2 short chain dehydrogenase/reductase family 8C, member 1	Homo sapiens (human)	Addison's disease Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Clouston syndrome D-bifunctional protein deficiency Friedreich ataxia Laron syndrome Perrault syndrome Pick's disease Refsum disease Reye syndrome Stiff-Person syndrome Turner syndrome West syndrome Zellweger syndrome achondroplasia adrenal carcinoma adrenal cortex cancer adrenal cortical hypofunction adrenocortical carcinoma adrenoleukodystrophy alpha-methylacyl-CoA racemase deficiency androgen insensitivity syndrome beta-ketothiolase deficiency blindness breast cancer breast carcinoma cancer carnitine palmitoyltransferase I deficiency cerebellar ataxia cerebellar disease cerebral degeneration cholestasis clubfoot colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital bile acid synthesis defect 4 congenital nystagmus craniosynostosis cystic kidney disease diabetic ketoacidosis dissociated nystagmus endometrial cancer endometrial carcinoma epilepsy essential hypertension gonadal dysgenesis hepatocellular carcinoma hereditary ataxia hydrocephalus hypertension hypertropia infantile Refsum disease large intestine cancer leukodystrophy lipid metabolism disorder liver cancer liver carcinoma mechanical strabismus non-congenital cyst of kidney obesity obsolete infantile epileptic encephalopathy obsolete type 1 diabetes mellitus 9 ophthalmoplegia osteoporosis pathologic nystagmus peroxisomal disease peroxisome biogenesis disorder 1A polycystic ovary syndrome polyhydramnios premature menopause primary cerebellar degeneration primary ovarian insufficiency prostate cancer prostate carcinoma rhizomelic chondrodysplasia punctata type 1 scoliosis seminoma sensorineural hearing loss spontaneous ocular nystagmus steatotic liver disease strabismus testicular cancer testicular germ cell cancer type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus uterine corpus cancer visual epilepsy
10908	patatin like phospholipase domain containing 6	PNPLA6 Aliases: NTE SPG39 iPLA2delta neuropathy target esterase sws	Homo sapiens (human)	Bardet-Biedl syndrome Boucher-Neuhauser syndrome Brooke-Spiegler syndrome Charcot-Marie-Tooth disease type 5 Henoch-Schoenlein purpura Kallmann syndrome Klinefelter syndrome Laron syndrome Laurence-Moon syndrome Leber congenital amaurosis MASA syndrome MYH-9 related disease Mast syndrome Oliver-McFarlane syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Patau syndrome Peutz-Jeghers syndrome SPOAN syndrome Sheehan syndrome Stargardt disease Troyer syndrome achondroplasia adiposis dolorosa alopecia alternating hemiplegia of childhood amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anterior horn cell disease autonomic neuropathy autosomal dominant cerebellar ataxia autosomal recessive congenital ichthyosis 1 autosomal recessive distal hereditary motor neuronopathy 1 autosomal recessive polycystic kidney disease biliary tract disease blindness blue cone monochromacy cancer cataract cavernous hemangioma central nervous system disease cerebellar ataxia cerebellar disease chorioangioma coloboma cone-rod dystrophy congenital nystagmus craniosynostosis critical illness polyneuropathy cryptorchidism dementia depressive disorder diabetes mellitus diabetic autonomic neuropathy diabetic neuropathy diabetic polyneuropathy dissociated nystagmus dysthymic disorder embryoma epilepsy focal epilepsy fundus albipunctatus fundus dystrophy glomus tumor gynecomastia hemangioma hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia histiocytoid hemangioma hypersensitivity vasculitis hypertrophy of breast hypertropia hypogonadism hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism ichthyosis infant gynecomastia inflammatory and toxic neuropathy intellectual disability intramuscular hemangioma isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency keratosis follicularis kidney failure lateral sclerosis learning disability lipomatosis liver cirrhosis lymphangioma major depressive disorder mechanical strabismus melancholic depression meningoencephalitis migraine without aura mongolian spot motor neuron disease multiple symmetric lipomatosis muscular atrophy nervous system disease neuroblastoma neurodegenerative disease neuropathy neurotic disorder obesity obsolete asthenopia obsolete congenital ichthyosiform erythroderma obsolete melancholia obsolete multiple symmetrical lipomatosis obstructive jaundice ophthalmoplegia optic atrophy panhypopituitarism paraplegia partial motor epilepsy pathologic nystagmus peripheral nervous system disease placental insufficiency polycystic kidney disease 4 polydactyly polyneuropathy progressive muscular atrophy pseudoxanthoma elasticum recurrent hypersomnia retinal degeneration retinitis pigmentosa sensorineural hearing loss sick building syndrome speech disorder spontaneous ocular nystagmus steatotic liver disease strabismus type 2 diabetes mellitus viral infectious disease visual epilepsy von Hippel-Lindau disease
54480	chondroitin polymerizing factor 2	CHPF2 Aliases: CSGlcA-T ChSy-3 KIAA1402 chondroitin sulfate glucuronyltransferase	Homo sapiens (human)	cancer colorectal cancer colorectal carcinoma embryoma large intestine cancer
10956	OS9 endoplasmic reticulum lectin	OS9 Aliases: ERLEC2 OS-9 endoplasmic reticulum lectin 2 erlectin 2	Homo sapiens (human)	cancer epithelioid sarcoma melanoma rheumatoid arthritis sarcoma skin melanoma spindle cell sarcoma
8809	interleukin 18 receptor 1	IL18R1 Aliases: CD218a IL-1Rrp IL1RRP	Homo sapiens (human)	Burkitt lymphoma CD40 ligand deficiency Clostridium difficile colitis Crohn's colitis Crohn's disease Graves' disease HELLP syndrome Holt-Oram syndrome Klippel-Trenaunay syndrome MHC class II deficiency Muckle-Wells syndrome Nezelof syndrome Norum disease Richter's syndrome Rubinstein-Taybi syndrome Sezary's disease Sjogren's syndrome T-cell acute lymphoblastic leukemia Tangier disease VACTERL association X-linked severe combined immunodeficiency abdominal aortic aneurysm abetalipoproteinemia acoustic neuroma acute lymphoblastic leukemia acute myeloid leukemia acute myocardial infarction acute promyelocytic leukemia adenosine deaminase deficiency adult acute lymphocytic leukemia aggressive NK-cell leukemia alcohol dependence alcohol use disorder alcoholic hepatitis allergic asthma allergic disease allergic rhinitis amyotrophic lateral sclerosis angiomatous meningioma ankylosing spondylitis anthracosilicosis anthracosis arrhythmogenic right ventricular cardiomyopathy arteriosclerotic cardiovascular disease arthritis arthropathy asbestosis ascending cholangitis asthma atherosclerosis atopic dermatitis atypical chronic myeloid leukemia, BCR-ABL1 negative autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome autoimmune thyroiditis autosomal dominant familial periodic fever bacterial infectious disease benign ependymoma benign meningioma bipolar disorder bladder carcinoma bone marrow cancer bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma brucellosis cancer cardiovascular system disease cavernous hemangioma celiac disease cellular ependymoma central nervous system cancer cerebral convexity meningioma cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervix carcinoma childhood acute lymphocytic leukemia childhood leukemia childhood osteosarcoma cholangitis choreaacanthocytosis chorioangioma chromophobe renal cell carcinoma chronic eosinophilic leukemia chronic lymphocytic leukemia chronic monocytic leukemia chronic myeloid leukemia chronic obstructive pulmonary disease clear cell meningioma clear cell renal cell carcinoma colitis collecting duct carcinoma colorectal cancer colorectal carcinoma combined T cell and B cell immunodeficiency common variable immunodeficiency complement deficiency contagious pustular dermatitis coronary artery disease coronary thrombosis cowpox depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy dysentery eclampsia embryoma endocrine exophthalmos endometriosis of uterus endometriosis eosinophilic esophagitis erythema infectiosum esophageal cancer esophageal carcinoma esophagitis essential thrombocythemia exanthema subitum fibrous meningioma gastritis gastroenteritis gastroesophageal reflux disease giant cell glioblastoma glioblastoma gliosarcoma glomus tumor goiter head and neck squamous cell carcinoma heart disease hemangioma hematopoietic system disease hepatitis B hepatocellular carcinoma high grade glioma histiocytoid hemangioma hypereosinophilic syndrome hyperthyroidism hypolipoproteinemia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis immune system disease inflammatory bowel disease 1 inflammatory bowel disease influenza intermediate coronary syndrome interstitial nephritis intestinal infectious disease intramuscular hemangioma intraorbital meningioma intraventricular meningioma intrinsic asthma irritable bowel syndrome juvenile myelomonocytic leukemia keratoconjunctivitis sicca large intestine cancer leech infestation leiomyoma leprosy leukemia liver cancer luminal breast carcinoma A lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma lymphangioma lymphoblastic lymphoma lymphoid leukemia lymphoplasmacyte-rich meningioma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 malaria maturity-onset diabetes of the young measles melanoma meningioma meningothelial meningioma microcystic meningioma microphthalmia with limb anomalies milker's nodule mixed glioma multiple sclerosis mumps myasthenia gravis myelodysplastic syndrome myelofibrosis myeloid leukemia myeloproliferative neoplasm myiasis myocardial infarction myofibroma myotonic dystrophy type 2 myxopapillary ependymoma nail-patella syndrome neuroblastoma neurocirculatory asthenia nonpapillary renal cell carcinoma obsolete melancholia obsolete type 1 diabetes mellitus 9 obstructive sleep apnea olfactory groove meningioma ophthalmia neonatorum ornithosis osteoarthritis osteomyelitis osteosarcoma pancreatic cancer pancreatic carcinoma papillary ependymoma papillary renal cell carcinoma parapsoriasis parasagittal meningioma peptic esophagitis periodontal disease periodontitis pituitary adenoma plasmacytoma polycythemia vera polycythemia pre-eclampsia primary biliary cholangitis primary cutaneous amyloidosis primary immunodeficiency disease primary pulmonary hypertension primary sclerosing cholangitis progressive muscular atrophy psammomatous meningioma psoriasis pulmonary emphysema pulmonary fibrosis pulmonary sarcoidosis pulpitis pustulosis of palm and sole pyelitis pyelonephritis red-green color blindness renal carcinoma renal cell carcinoma respiratory syncytial virus infectious disease rheumatoid arthritis rubella sarcoidosis sarcomatoid renal cell carcinoma schizophrenia sclerosing cholangitis secretory meningioma seminoma severe acute respiratory syndrome severe combined immunodeficiency silent myocardial infarction skin melanoma smallpox spinal meningioma split hand-foot malformation 1 with sensorineural hearing loss stomach cancer stomach carcinoma suppurative cholangitis systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic lupus erythematosus tanycytic ependymoma testicular cancer testicular germ cell cancer testis seminoma thrombocytopenia-absent radius syndrome thyroid gland anaplastic carcinoma thyroid gland disease thyrotoxicosis toxoplasmosis trachoma transitional meningioma tuberculosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis urinary bladder cancer uterine fibroid uveoparotid fever variola major variola minor vasomotor rhinitis
56548	carbohydrate sulfotransferase 7	CHST7 Aliases: C6ST-2 C6ST2	Homo sapiens (human)	bronchus cancer bronchus carcinoma colorectal cancer colorectal carcinoma large intestine cancer lung benign neoplasm lung cancer lung carcinoma pneumonia
93432	maltase-glucoamylase 2 (putative)	MGAM2	Homo sapiens (human)
80168	monoacylglycerol O-acyltransferase 2	MOGAT2 Aliases: DGAT2L5 FLJ22644 MGAT2	Homo sapiens (human)	diabetes mellitus diabetic ketoacidosis disease of metabolism glucose intolerance hepatocellular carcinoma liver cancer prediabetes syndrome type 2 diabetes mellitus
2525	fucosyltransferase 3 (Lewis blood group)	FUT3 Aliases: CD174 galactoside 3(4)-L-fucosyltransferase	Homo sapiens (human)	Crohn's colitis Crohn's disease achalasia adult respiratory distress syndrome alopecia anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis bile duct adenocarcinoma bile duct carcinoma bipolar disorder bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer candidiasis carcinoma childhood leukemia childhood osteosarcoma cholangiocarcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma colitis collecting duct carcinoma colon adenocarcinoma colon carcinoma colorectal cancer colorectal carcinoma congenital diaphragmatic hernia coronary artery disease cystic fibrosis depressive disorder dilated cardiomyopathy 1A dilated cardiomyopathy embryoma esophagitis gastroenteritis gastroesophageal reflux disease herpes simplex hiatus hernia ileitis ileocolitis immunoglobulin alpha deficiency inflammatory bowel disease 1 inflammatory bowel disease intrahepatic cholangiocarcinoma invasive ductal carcinoma large intestine cancer leech infestation leukemia lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease macrocytic anemia major depressive disorder megaesophagus melancholic depression microphthalmia myiasis nonpapillary renal cell carcinoma nutmeg liver obsolete Matthew-Wood syndrome obsolete melancholia osteosarcoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma peptic esophagitis primary sclerosing cholangitis prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma rumination disorder sarcomatoid carcinoma sarcomatoid renal cell carcinoma sclerosing cholangitis selective IgA deficiency disease stomach cancer stomach carcinoma toxoplasmosis ulcerative colitis
64132	xylosyltransferase 2	XYLT2 Aliases: PXYLT2 XT-II protein xylosyltransferase 2	Homo sapiens (human)	Cockayne syndrome Cornelia de Lange syndrome Desbuquois dysplasia Dubowitz syndrome Ewing sarcoma Gilbert syndrome Meckel syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome T-cell acute lymphoblastic leukemia X-linked Aarskog syndrome acute biphenotypic leukemia acute leukemia acute myocardial infarction age related macular degeneration amblyopia angioid streaks ataxia telangiectasia atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant polycystic kidney disease autosomal recessive Robinow syndrome bacterial infectious disease bilirubin metabolic disorder bladder carcinoma blindness brain stem infarction cancer cannabis abuse cannabis dependence cataract cerebral artery occlusion cerebral infarction cerebrovascular disease cholera chondrodysplasia-pseudohermaphroditism syndrome chronic kidney disease chronic monocytic leukemia chronic myelomonocytic leukemia clubfoot congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital nystagmus congestive heart failure coronary thrombosis degeneration of macula and posterior pole depressive disorder diabetes mellitus diabetic ketoacidosis dissociated nystagmus dysthymic disorder embryoma essential hypertension gallbladder disease glomerulonephritis hepatic veno-occlusive disease hepatitis B herpes simplex hypertension intellectual disability intermittent claudication juvenile myelomonocytic leukemia keratosis follicularis kidney disease kidney failure learning disability lichen disease lipoatrophic diabetes mellitus lipodystrophy liver disease localized scleroderma macular degeneration major depressive disorder melancholic depression microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microphthalmia mitral valve insufficiency mitral valve prolapse mitral valve stenosis mongolian spot myocardial infarction myopia nephritis nephrosis neurotic disorder obesity obsolete melancholia obsolete type 1 diabetes mellitus 9 osteoporosis papilloma patent foramen ovale pathologic nystagmus pleomorphic adenoma pneumocystosis polycystic kidney disease postural orthostatic tachycardia syndrome pseudoxanthoma elasticum psoriatic arthritis pyoureter restrictive cardiomyopathy retinal detachment scleroderma sensorineural hearing loss silent myocardial infarction skin benign neoplasm skin cancer spontaneous ocular nystagmus squamous cell papilloma steatotic liver disease strabismic amblyopia systemic scleroderma thrombocytopenia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus urinary bladder cancer ventricular septal defect viral infectious disease xeroderma pigmentosum group A xeroderma pigmentosum group B xeroderma pigmentosum group C xeroderma pigmentosum group D xeroderma pigmentosum group E xeroderma pigmentosum group F xeroderma pigmentosum group G xeroderma pigmentosum variant type xeroderma pigmentosum
6785	ELOVL fatty acid elongase 4	ELOVL4 Aliases: CT118 cancer/testis antigen 118	Homo sapiens (human)	Kuhnt-Junius degeneration Leber congenital amaurosis Sjogren-Larsson syndrome Stargardt disease achromatopsia acquired color blindness acquired hyperkeratosis acute myocardial infarction age related macular degeneration alternating hemiplegia of childhood angioedema anhidrosis autonomic neuropathy autosomal dominant cerebellar ataxia autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis blindness blue color blindness cancer cardiac arrest central nervous system disease cerebellar ataxia cerebellar disease color blindness cone-rod dystrophy 2 cone-rod dystrophy 7 cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness corneal dystrophy coronary thrombosis degeneration of macula and posterior pole diabetes mellitus diabetic ketoacidosis dissociated nystagmus dry eye syndrome epilepsy erythrokeratodermia variabilis et progressiva 1 erythrokeratodermia variabilis eye disease fundus albipunctatus glycogen storage disease II granuloma annulare hepatocellular carcinoma hypertropia hypohidrosis ichthyosis inguinal hernia keratosis follicularis liver cancer locked-in syndrome macular degeneration mechanical strabismus mongolian spot myocardial infarction nervous system disease neurodegenerative disease night blindness obsolete congenital ichthyosiform erythroderma ophthalmoplegia pathologic nystagmus pseudoxanthoma elasticum quadriplegia red color blindness red-green color blindness retinitis pigmentosa 25 retinitis pigmentosa 30 retinitis pigmentosa silent myocardial infarction skin disease spinocerebellar ataxia type 34 spontaneous ocular nystagmus strabismus thrombocytopenia type 2 diabetes mellitus urticaria visual epilepsy xerophthalmia
142	poly(ADP-ribose) polymerase 1	PARP1 Aliases: ARTD1 PARP PARS Poly-PARP	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 3 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Balo concentric sclerosis Barrett's esophagus Burkitt lymphoma Chagas disease Cockayne syndrome Cornelia de Lange syndrome Crohn's colitis Crohn's disease Down syndrome Dubowitz syndrome Duchenne muscular dystrophy Ewing sarcoma Fanconi anemia complementation group A Fanconi anemia Gilles de la Tourette syndrome Graves' disease Hailey-Hailey disease Henoch-Schoenlein purpura Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease IgA glomerulonephritis Keshan disease Langerhans-cell histiocytosis Lynch syndrome MHC class II deficiency Marinesco-Sjogren syndrome Meniere's disease Nijmegen breakage syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 2 Parkinson's disease 4 Parkinson's disease Patau syndrome Peyronie's disease Pick's disease Prader-Willi syndrome Reye syndrome Richter's syndrome Robinow syndrome Rothmund-Thomson syndrome Seckel syndrome Sertoli cell-only syndrome Sezary's disease Silver-Russell syndrome Stevens-Johnson syndrome T-cell acute lymphoblastic leukemia Treacher Collins syndrome Warsaw breakage syndrome Weissenbacher-Zweymuller syndrome Werner syndrome X-linked Aarskog syndrome X-linked ichthyosis Y-linked spermatogenic failure 1 Zika fever abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 acquired immunodeficiency syndrome acrodermatitis acute biphenotypic leukemia acute leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adenosarcoma adenosine deaminase deficiency adrenal gland cancer adrenoleukodystrophy adult fibrosarcoma adult medulloblastoma age related macular degeneration agranulocytosis alexia allergic asthma allergic rhinitis alopecia alternating hemiplegia of childhood amnestic disorder amyloidosis amyotrophic lateral sclerosis anaplastic astrocytoma androgen insensitivity syndrome androgenic alopecia anemia anthrax disease anxiety disorder arachnoiditis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma ataxia with oculomotor apraxia type 1 atelosteogenesis atherosclerosis atrial fibrillation autoimmune disease autoimmune lymphoproliferative syndrome autonomic neuropathy autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive Robinow syndrome autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy bacterial meningitis bacterial sepsis balanitis xerotica obliterans benign mesothelioma bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bladder urothelial carcinoma bone marrow cancer bone osteosarcoma borna disease botryoid rhabdomyosarcoma brachydactyly type B1 brachydactyly brain cancer brain ischemia brain stem infarction breast adenocarcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy cardiovascular system disease celiac disease central nervous system cancer central nervous system disease central nervous system lymphoma cerebellar ataxia cerebellar disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood acute lymphocytic leukemia childhood astrocytic tumor childhood cerebral astrocytoma childhood germ cell cancer childhood leukemia childhood medulloblastoma childhood osteosarcoma childhood pilocytic astrocytoma cholangiocarcinoma chondrodysplasia-pseudohermaphroditism syndrome chondrosarcoma chordoma chromophobe renal cell carcinoma chronic fatigue syndrome chronic interstitial cystitis chronic kidney disease chronic lymphocytic leukemia chronic monocytic leukemia chronic myeloid leukemia chronic myelomonocytic leukemia chronic obstructive pulmonary disease clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart congenital muscular dystrophy congestive heart failure corneal disease coronary artery disease coronary thrombosis cribriform carcinoma cutaneous fibrous histiocytoma cutis laxa deafness-dystonia-optic neuronopathy syndrome dedifferentiated liposarcoma degeneration of macula and posterior pole denture stomatitis depressive disorder dermatitis diabetes mellitus diabetic autonomic neuropathy diabetic cataract diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy diabetic retinopathy differentiated thyroid gland carcinoma diffuse large B-cell lymphoma disease of metabolism dissociative amnesia distal arthrogryposis distal myopathy duodenum cancer dyslexia dysplastic nevus syndrome dysthymic disorder embryoma embryonal cancer embryonal rhabdomyosarcoma encephalitis encephalomyelitis endocrine exophthalmos endolymphatic hydrops endometrial adenocarcinoma endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis endomyocardial fibrosis epilepsy epithelioid leiomyosarcoma epithelioid malignant peripheral nerve sheath tumor epithelioid sarcoma esophageal cancer esophageal carcinoma esophagus adenocarcinoma esophagus small cell carcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia eye disease facioscapulohumeral muscular dystrophy familial adenomatous polyposis 1 familial adenomatous polyposis familiar ovarian carcinoma fibrillary astrocytoma fibrosarcoma follicular adenoma frozen shoulder gastroenteritis gastrointestinal system disease gemistocytic astrocytoma generalized anxiety disorder germ cell and embryonal cancer germ cell cancer germinoma giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glycogen storage disease II goiter granular cell carcinoma granular corneal dystrophy 2 head and neck cancer head and neck squamous cell carcinoma heart cancer heart disease hematologic cancer hepatitis A hepatitis B hepatitis hepatoblastoma hepatocellular carcinoma hereditary breast ovarian cancer syndrome hidradenoma high grade glioma human immunodeficiency virus infectious disease hypereosinophilic syndrome hyperglycemia hypersensitivity vasculitis hypertension hyperthyroidism hypertrophic cardiomyopathy hypoparathyroidism-deafness-renal disease syndrome idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis immune system disease inflammatory bowel disease 1 inflammatory bowel disease inflammatory breast carcinoma intellectual disability intermediate coronary syndrome interstitial cystitis intestinal disease intracranial aneurysm intrahepatic cholangiocarcinoma intrinsic asthma islet cell tumor juvenile myelomonocytic leukemia juvenile pilocytic astrocytoma keratoconus kidney disease kidney failure large cell medulloblastoma large intestine cancer laryngeal squamous cell carcinoma learning disability leiomyoma leiomyosarcoma leukemia leukopenia limb-girdle muscular dystrophy liposarcoma liver cancer liver carcinoma liver cirrhosis luminal breast carcinoma A lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma lung squamous cell carcinoma lupus erythematosus lymphangioleiomyomatosis lymphoma macrocytic anemia macular degeneration major depressive disorder mal de Meleda malignant astrocytoma malignant mesothelioma malignant peripheral nerve sheath tumor malignant pleural mesothelioma mantle cell lymphoma medulloblastoma medullomyoblastoma melancholic depression melanoma melanotic medulloblastoma meningitis microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcystic adenoma microphthalmia middle cerebral artery infarction mitochondrial DNA depletion syndrome mixed glioma monoclonal gammopathy of uncertain significance multiple myeloma multiple sclerosis muscular dystrophy myelitis myelodysplastic syndrome myeloproliferative neoplasm myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 myxoid leiomyosarcoma narcolepsy nasopharynx carcinoma nephritis nephroblastoma nephrosis nervous system disease neurilemmoma neuroblastoma neurodegenerative disease neuroendocrine carcinoma neuroendocrine tumor neurofibrosarcoma neuronal ceroid lipofuscinosis 1 neurotic disorder neutropenia nodular nonsuppurative panniculitis non-Hodgkin lymphoma nonpapillary renal cell carcinoma obesity obsolete Matthew-Wood syndrome obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete melancholia obsolete precursor B lymphoblastic lymphoma/leukemia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma oculopharyngeal muscular dystrophy oligospermia osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma panniculitis papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma paraganglioma parapsoriasis patent ductus arteriosus perinatal necrotizing enterocolitis peritoneal carcinoma pheochromocytoma phobic disorder phototoxic dermatitis pilocytic astrocytoma pleomorphic liposarcoma pneumonia premature menopause primary cerebellar degeneration primary cutaneous amyloidosis primary immunodeficiency disease primary open angle glaucoma primary pulmonary hypertension proctitis progeria progressive multifocal leukoencephalopathy progressive muscular atrophy prostate cancer prostate carcinoma protoplasmic astrocytoma prune belly syndrome psoriasis pulmonary emphysema pustulosis of palm and sole pyoureter rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma respiratory failure restrictive dermopathy reticulosarcoma retinal disease retinitis retrograde amnesia rhabdomyosarcoma rheumatic fever rheumatoid arthritis rippling muscle disease 2 sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia scleroderma secondary Parkinson disease senile cataract severe combined immunodeficiency severe congenital neutropenia silent myocardial infarction skin benign neoplasm skin cancer skin melanoma skin papilloma skin tag small intestine cancer spindle cell sarcoma sporadic breast cancer squamous cell carcinoma status epilepticus steatotic liver disease stomach cancer stomach carcinoma stomatitis subependymal giant cell astrocytoma syringoma systemic lupus erythematosus systemic scleroderma teratocarcinoma thymic carcinoma thymoma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland disease thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma transient cerebral ischemia trigeminal neuralgia trypanosomiasis tubular adenocarcinoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis ulcerative stomatitis uremia ureteral obstruction urinary bladder cancer uterine corpus cancer uterine fibroid uveal melanoma vasomotor rhinitis vertebrobasilar insufficiency viral infectious disease viral meningitis vitiligo xeroderma pigmentosum group A
3965	galectin 9	LGALS9 Aliases: LGALS9A	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Barrett's esophagus Burkitt lymphoma Chagas disease Crohn's colitis Crohn's disease Evans' syndrome Graves' disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Japanese encephalitis Kimura disease Niemann-Pick disease type C1 Niemann-Pick disease Pick's disease Reye syndrome Richter's syndrome T-cell acute lymphoblastic leukemia acquired immunodeficiency syndrome acrodermatitis acute myeloid leukemia acute myocarditis adult T-cell leukemia/lymphoma allergic asthma antiphospholipid syndrome aplastic anemia arthritis arthropathy asthma autoimmune disease autoimmune hepatitis autoimmune lymphoproliferative syndrome autoimmune thrombocytopenic purpura benign mesothelioma bile duct adenocarcinoma bile duct carcinoma bladder urothelial carcinoma breast cancer breast carcinoma bronchiectasis bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer central nervous system lymphoma cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood type dermatomyositis cholangiocarcinoma chordoma chorioangioma chromophobe renal cell carcinoma chronic fatigue syndrome chronic lymphocytic leukemia chronic myeloid leukemia chronic obstructive pulmonary disease clear cell adenocarcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cutaneous fibrous histiocytoma dengue disease dermatitis dermatomyositis embryoma encephalitis encephalomyelitis endometrial adenocarcinoma endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis esophageal cancer esophageal carcinoma esophagus adenocarcinoma esophagus squamous cell carcinoma essential thrombocythemia exanthem extrinsic allergic alveolitis farmer's lung female reproductive system disease gallbladder disease gastrointestinal system cancer giant cell glioblastoma glaucoma glioblastoma gliosarcoma glomerulonephritis head and neck squamous cell carcinoma hemangioma hepatitis A hepatitis B hepatitis C hepatitis hepatocellular carcinoma herpes simplex hidradenoma high grade glioma histiocytoid hemangioma human immunodeficiency virus infectious disease hypereosinophilic syndrome hyperthyroidism immune system disease immune-complex glomerulonephritis inflammatory bowel disease 1 inflammatory bowel disease influenza intracranial aneurysm intrahepatic cholangiocarcinoma intramuscular hemangioma intrinsic asthma kidney disease large intestine cancer liver cancer liver carcinoma liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lupus erythematosus lupus nephritis lymphoma malignant mesothelioma melanoma mixed glioma multiple myeloma multiple sclerosis myelitis myelodysplastic syndrome myocarditis nasopharynx carcinoma nephritis nonpapillary renal cell carcinoma obsolete T-cell lymphoblastic leukemia/lymphoma obsolete ymphosarcoma osteoarthritis pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma patent ductus arteriosus periodontal disease pneumonia portal hypertension primary cutaneous T-cell non-Hodgkin lymphoma pulmonary emphysema renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma scleroderma skin benign neoplasm skin cancer skin epithelioid hemangioma skin melanoma skin papilloma skin tag skull base chordoma squamous cell carcinoma stomach cancer stomach carcinoma syringoma systemic lupus erythematosus systemic scleroderma thromboangiitis obliterans thyrotoxicosis tongue squamous cell carcinoma transitional cell carcinoma trypanosomiasis tuberculosis ulcerative colitis uterine corpus cancer viral infectious disease yellow fever

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