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 **1326 - 1350** of **1582** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▼	Disease Ontology
161357	MAM domain containing glycosylphosphatidylinositol anchor 2	MDGA2	Homo sapiens (human)	Balo concentric sclerosis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease adrenoleukodystrophy benign epilepsy with centrotemporal spikes cancer central nervous system disease dissociative disorder embryoma microinvasive gastric cancer narcolepsy neurotic disorder rheumatoid arthritis sexual dysfunction stomach cancer stomach carcinoma systemic lupus erythematosus
497190	C-type lectin domain family 18 member B	CLEC18B	Homo sapiens (human)	acquired immunodeficiency syndrome cancer embryoma giant cell glioblastoma glioblastoma high grade glioma
6309	sterol-C5-desaturase	SC5D Aliases: delta(7)-sterol 5(6)-desaturase lathosterol oxidase	Homo sapiens (human)	Marfan syndrome Peters anomaly Smith-Lemli-Opitz syndrome Unverricht-Lundborg syndrome basal cell carcinoma blepharospasm cataract cleft palate clubfoot complex partial epilepsy congenital heart disease congenital ptosis cornea plana early myoclonic encephalopathy epilepsy focal hand dystonia gallbladder disease gingival hypertrophy gingival overgrowth intellectual disability intrahepatic cholestasis isolated cleft palate learning disability liver disease meningocele microcephaly placental insufficiency polydactyly ptosis sensorineural hearing loss situs inversus temporal lobe epilepsy thrombocytopenia tuberous sclerosis visual epilepsy
307	annexin A4	ANXA4	Homo sapiens (human)	acute myeloid leukemia adenomatoid tumor alcohol use disorder allergic asthma asthma atrial fibrillation benign mesothelioma bile duct adenocarcinoma bile duct carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cholangiocarcinoma chromophobe renal cell carcinoma clear cell adenocarcinoma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma depressive disorder dysthymic disorder embryoma hepatocellular carcinoma intrahepatic cholangiocarcinoma intrinsic asthma large intestine cancer liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder malaria malignant mesothelioma melancholic depression neurotic disorder nonpapillary renal cell carcinoma obsolete melancholia ovarian cancer ovarian carcinoma ovarian clear cell adenocarcinoma ovary serous adenocarcinoma papillary adenocarcinoma papillary renal cell carcinoma prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma stomach cancer stomach carcinoma thyroid gland papillary carcinoma
171169	sperm acrosome associated 4	SPACA4 Aliases: SAMP14	Homo sapiens (human)
178	amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase	AGL Aliases: GDE glycogen debranching enzyme glycogen storage disease type III	Homo sapiens (human)	Duchenne muscular dystrophy Laron syndrome achondroplasia acute promyelocytic leukemia atrichia with papular lesions 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 bladder carcinoma cancer cardiomyopathy colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital muscular dystrophy cystinuria disease of metabolism distal myopathy endomyocardial fibrosis facioscapulohumeral muscular dystrophy familial hyperlipidemia familial partial lipodystrophy familial periodic paralysis galactosemia giardiasis glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease III glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hepatitis C hypertrophic cardiomyopathy hypoglycemia isolated elevated serum creatine phosphokinase levels kidney failure large intestine cancer limb-girdle muscular dystrophy lipoatrophic diabetes mellitus lipodystrophy liver cirrhosis lung cancer lung non-small cell carcinoma muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy nodular nonsuppurative panniculitis 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 oculopharyngeal muscular dystrophy panniculitis primary immunodeficiency disease rippling muscle disease 2 uremia urinary bladder cancer
5500	protein phosphatase 1 catalytic subunit beta	PPP1CB	Homo sapiens (human)	Noonan syndrome-like disorder with loose anagen hair 2 cancer
150763	glycerol-3-phosphate acyltransferase 2, mitochondrial	GPAT2 Aliases: CT123 cancer/testis antigen 123	Homo sapiens (human)	adrenoleukodystrophy breast cancer breast carcinoma cancer melanoma skin melanoma
200576	phosphoinositide kinase, FYVE-type zinc finger containing	PIKFYVE Aliases: FAB1 KIAA0981 MGC40423 PIP5K ZFYVE29 p235 zinc finger, FYVE domain containing 29	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 B-cell lymphoma Crohn's colitis Crohn's disease Fleck corneal dystrophy Pick's disease Reye syndrome breast cancer cancer cardiomyopathy cerebral degeneration embryoma endomyocardial fibrosis gestational diabetes hypertrophic cardiomyopathy legionellosis multiple myeloma obsolete asthenopia obsolete ymphosarcoma pneumonia transitional cell carcinoma
79147	fukutin related protein	FKRP Aliases: FKTR LGMD2I MDC1C	Homo sapiens (human)	Axenfeld-Rieger syndrome Becker muscular dystrophy Bell's palsy Bethlem myopathy Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Richter's syndrome Walker-Warburg syndrome X-linked dilated cardiomyopathy agnosia amnestic 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 bilateral optic nerve hypoplasia blindness buphthalmos campomelic dysplasia cardiomyopathy cataract catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia 2 catecholaminergic polymorphic ventricular tachycardia 3 catecholaminergic polymorphic ventricular tachycardia 4 catecholaminergic polymorphic ventricular tachycardia 5 catecholaminergic polymorphic ventricular tachycardia central nervous system origin vertigo centronuclear myopathy chronic lymphocytic leukemia cleft lip cleft palate coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cone-rod dystrophy congenital heart disease congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy-dystroglycanopathy type A5 congenital muscular dystrophy congenital myopathy 1A congenital myopathy 4A congenital structural myopathy congestive heart failure cornea plana cortical dysplasia-focal epilepsy syndrome craniometaphyseal dysplasia cryptorchidism developmental coordination disorder diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy distal myopathy endomyocardial fibrosis epilepsy facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy familial periodic paralysis fibromyalgia fundus albipunctatus fundus dystrophy glaucoma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hydrophthalmos hypertrophic cardiomyopathy hypertropia imperforate anus intellectual disability isolated cleft palate isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly mechanical strabismus megaconial type congenital muscular dystrophy megalocornea meningocele microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia myositis nemaline myopathy neuromuscular 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 type 1 diabetes mellitus 9 obstructive hydrocephalus oculopharyngeal muscular dystrophy ophthalmoplegia optic atrophy peripheral retinal degeneration pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 pseudosarcomatous fibromatosis recurrent corneal erosion renal agenesis retinal detachment retinitis pigmentosa retrograde amnesia rigid spine muscular dystrophy 1 rippling muscle disease 2 scoliosis senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly speech disorder strabismus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability Najm type 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 visual epilepsy
9488	phosphatidylinositol glycan anchor biosynthesis class B	PIGB Aliases: GPI mannosyltransferase 3 GPI-MT-III PIG-B dol-P-Man dependent GPI mannosyltransferase III	Homo sapiens (human)	axonal neuropathy developmental and epileptic encephalopathy 80 epilepsy intellectual disability learning disability sleeping sickness visual epilepsy
10331	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3	B3GNT3 Aliases: B3GN-T3 B3GNT-3 HP10328 beta-1,3-N-acetylglucosaminyltransferase bGnT-3 beta3Gn-T3 putative type II membrane protein transmembrane protein 3	Homo sapiens (human)	cancer cervical adenocarcinoma cervical cancer cervix carcinoma common wart embryoma influenza lung cancer lung non-small cell carcinoma neuroblastoma
3707	inositol-trisphosphate 3-kinase B	ITPKB Aliases: IP3-3KB IP3KB	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 B-cell lymphoma Pick's disease Reye syndrome allergic disease bronchus cancer bronchus carcinoma cancer cerebral degeneration dental caries dentin caries embryoma lung benign neoplasm lung cancer lung carcinoma obsolete ymphosarcoma sick sinus syndrome
4124	mannosidase alpha class 2A member 1	MAN2A1 Aliases: GOLIM7 golgi integral membrane protein 7	Homo sapiens (human)	autoimmune disease autoimmune lymphoproliferative syndrome cancer childhood acute lymphocytic leukemia congenital dyserythropoietic anemia type II congenital dyserythropoietic anemia diabetes mellitus embryoma giant cell glioblastoma glioblastoma hepatocellular carcinoma high grade glioma immune system disease liver cancer prostate cancer prostate carcinoma schizophrenia systemic lupus erythematosus type 2 diabetes mellitus
11227	polypeptide N-acetylgalactosaminyltransferase 5	GALNT5 Aliases: GalNAc-T5 polypeptide GalNAc transferase 5	Homo sapiens (human)	breast cancer cancer embryoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma stomach cancer stomach carcinoma
1462	versican	VCAN Aliases: PG-M versican proteoglycan	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 Clouston syndrome Costello syndrome Duchenne muscular dystrophy Ehlers-Danlos syndrome spondylodysplastic type 2 Marfan syndrome Pick's disease Reye syndrome Smith-McCort dysplasia T-cell acute lymphoblastic leukemia abdominal aortic aneurysm acoustic neuroma acute biphenotypic leukemia acute interstitial pneumonia acute leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoid cystic carcinoma adenoma adult medulloblastoma alopecia anaplastic astrocytoma androgenic alopecia angiomatous meningioma aortic aneurysm arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis benign meningioma benign mesothelioma bladder carcinoma blindness bone osteosarcoma brain cancer brain disease breast cancer breast carcinoma bronchiolitis obliterans bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease cataract cellular schwannoma central nervous system cancer cerebral convexity meningioma cerebral degeneration cerebral infarction cerebrovascular disease childhood cerebral astrocytoma childhood kidney cell carcinoma childhood medulloblastoma childhood osteosarcoma chondrosarcoma choriocarcinoma chromophobe renal cell carcinoma chronic kidney disease chronic obstructive pulmonary disease ciliary body disease clear cell meningioma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis cutaneous fibrous histiocytoma dermatofibrosarcoma protuberans diabetic ketoacidosis embryoma endometrial cancer endometrial carcinoma endometriosis of ovary endometriosis of uterus endometriosis epithelioid leiomyosarcoma eye disease fibrillary astrocytoma fibrous meningioma focal segmental glomerulosclerosis follicular adenoma gastrointestinal stromal tumor gemistocytic astrocytoma gestational trophoblastic neoplasm glaucoma gliosarcoma glomerulonephritis heart disease hepatitis B hepatitis C hepatocellular carcinoma hidradenoma high grade glioma hyperglycemia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis inflammatory bowel disease 1 inflammatory bowel disease intermittent claudication intracranial aneurysm intraorbital meningioma intraventricular meningioma iris disease juvenile pilocytic astrocytoma kidney cancer kidney disease kidney failure large intestine cancer laryngeal benign neoplasm laryngeal carcinoma laryngeal disease laryngeal squamous cell carcinoma larynx cancer lateral meningocele syndrome leiomyoma leiomyosarcoma liver cancer liver carcinoma lung benign neoplasm lung cancer lung carcinoma lung disease malignant astrocytoma malignant epithelial mesothelioma malignant mesothelioma malignant peripheral nerve sheath tumor medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma melanotic neurilemmoma meningioma meningothelial meningioma microcystic adenoma microcystic meningioma microphthalmia mixed glioma multiple myeloma muscular dystrophy myocardial infarction myofibroma myopia myxoid leiomyosarcoma nephritis nephrosis neurilemmoma neuroblastoma neurodegenerative disease neuroendocrine carcinoma neuroendocrine tumor neurogenic arthropathy nodular prostate nonpapillary renal cell carcinoma obsolete Matthew-Wood syndrome obsolete type 1 diabetes mellitus 9 olfactory groove meningioma optic atrophy osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma panuveitis papillary adenoma papillary renal cell carcinoma parasagittal meningioma pilocytic astrocytoma pituitary adenoma placenta cancer plexiform schwannoma pneumonia polycystic ovary syndrome prostate adenocarcinoma prostate cancer prostate carcinoma prostatic adenoma protoplasmic astrocytoma psammomatous meningioma pulmonary emphysema pulmonary fibrosis pyoureter renal carcinoma renal cell carcinoma renal osteodystrophy salivary gland adenoid cystic carcinoma salivary gland cancer sarcomatoid carcinoma sarcomatoid renal cell carcinoma secretory meningioma silent myocardial infarction situs inversus skin benign neoplasm skin cancer skin melanoma skin papilloma skin tag spinal meningioma spondylitis spondyloarthropathy spondylosis stomach cancer stomach carcinoma subependymal giant cell astrocytoma syringoma tendinitis thoracic aortic aneurysm thyroid adenoma thyroid cancer thyroid gland carcinoma tracheal disease transitional meningioma tuberous sclerosis 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 ulcerative colitis urinary bladder cancer uterine corpus cancer uterine fibroid uveitis vascular disease
1272	contactin 1	CNTN1 Aliases: F3 GP135 glycoprotein gP135	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 Compton-North congenital myopathy Guillain-Barre syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Miller Fisher syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome adenocarcinoma adenoma arthritis arthropathy attention deficit hyperactivity disorder breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer cerebral degeneration chronic inflammatory demyelinating polyneuritis chronic inflammatory demyelinating polyradiculoneuropathy colorectal cancer colorectal carcinoma congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital myopathy 1A craniosynostosis cribriform carcinoma embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma familial adenomatous polyposis 1 familial adenomatous polyposis familial nephrotic syndrome familial periodic paralysis fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome gliosarcoma granular cell carcinoma high grade glioma islet cell tumor large intestine cancer lipoid nephrosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma megaconial type congenital muscular dystrophy membranous glomerulonephritis mixed glioma multiple sclerosis muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 myopathy nemaline myopathy nephrotic syndrome neuropathy peripheral nervous system disease placental insufficiency polyhydramnios polyneuropathy progressive muscular atrophy prostate cancer prostate carcinoma rigid spine muscular dystrophy 1 spinal muscular atrophy squamous cell carcinoma stomach cancer stomach carcinoma thyroid adenoma thyroid cancer thyroid gland carcinoma tongue squamous cell carcinoma tubular adenocarcinoma
2590	polypeptide N-acetylgalactosaminyltransferase 2	GALNT2 Aliases: GalNAc-T2 polypeptide GalNAc transferase 2	Homo sapiens (human)	Crohn's colitis Crohn's disease abdominal obesity-metabolic syndrome 1 achondroplasia acute myeloid leukemia arteriosclerotic cardiovascular disease atherosclerosis cancer central nervous system cancer cerebral infarction cerebrovascular disease cholesterol-ester transfer protein deficiency chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma congenital disorder of glycosylation type II coronary artery disease diabetes mellitus embryoma essential hypertension familial hyperlipidemia gastric adenocarcinoma gliosarcoma hepatocellular carcinoma high grade glioma hyperalphalipoproteinemia 1 hyperglycemia hypertension hypochondroplasia inflammatory bowel disease 1 inflammatory bowel disease liver cancer mixed glioma nutmeg liver obesity papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia squamous cell carcinoma stomach cancer stomach carcinoma temporal arteritis tongue squamous cell carcinoma type 2 diabetes mellitus ulcerative colitis
57462	myogenesis regulating glycosidase (putative)	MYORG Aliases: NET37	Homo sapiens (human)	amnestic disorder basal ganglia calcification choreatic disease dystonia epilepsy hydrocephalus lingual-facial-buccal dyskinesia microcephaly migraine neurodegenerative disease placental insufficiency recurrent corneal erosion retrograde amnesia secondary Parkinson disease syndromic X-linked intellectual disability type 10 thrombocytopenia visual epilepsy
64131	xylosyltransferase 1	XYLT1 Aliases: PXYLT1 XT-I protein xylosyltransferase 1	Homo sapiens (human)	Barber-Say syndrome Bernard-Soulier syndrome Brooke-Spiegler syndrome Desbuquois dysplasia Duchenne muscular dystrophy Ehlers-Danlos syndrome Laron syndrome abdominal aortic aneurysm achondroplasia acne acute myeloid leukemia age related macular degeneration anaplastic astrocytoma angioid streaks anodontia arthritis arthropathy cerebral infarction cerebrovascular disease childhood cerebral astrocytoma chondrodysplasia punctata cleft palate cleidocranial dysplasia clubfoot congestive heart failure degeneration of macula and posterior pole degenerative disc disease diabetes mellitus diabetic ketoacidosis enophthalmos essential hypertension fibrillary astrocytoma gemistocytic astrocytoma glaucoma glomerulonephritis high grade glioma humeroradial synostosis hypertension hypertrichosis hypotrichosis intellectual disability intermittent claudication isolated cleft palate isolated growth hormone deficiency juvenile pilocytic astrocytoma keratosis follicularis kidney disease kidney failure learning disability macular degeneration malignant astrocytoma microcephaly mitral valve insufficiency mitral valve prolapse mitral valve stenosis mongolian spot mucopolysaccharidosis IV multiple epiphyseal dysplasia muscular dystrophy myopia nephritis nephrosis obsolete exophthalmos obsolete type 1 diabetes mellitus 9 orbital disease osteoarthritis osteochondrodysplasia osteogenesis imperfecta pilocytic astrocytoma placental insufficiency pleomorphic adenoma postural orthostatic tachycardia syndrome protoplasmic astrocytoma pseudoxanthoma elasticum pyoureter qualitative platelet defect radioulnar synostosis restrictive cardiomyopathy scoliosis subependymal giant cell astrocytoma substance abuse substance-related disorder tooth agenesis 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 ventricular septal defect
239	arachidonate 12-lipoxygenase, 12S type	ALOX12 Aliases: 12S-LOX Arachidonate 12-lipoxygenase, 12S-type platelet 12-LOX	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 Becker muscular dystrophy Crohn's disease Duchenne muscular dystrophy Pick's disease Reye syndrome actinic keratosis acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adult lymphoma amyloidosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis 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 bacterial sepsis benign mesothelioma bipolar disorder bone marrow cancer breast cancer breast carcinoma cancer cardiovascular system disease central nervous system lymphoma cerebral degeneration cerebral infarction cerebrovascular disease childhood lymphoma chromophobe renal cell carcinoma clear cell renal cell carcinoma colitis collecting duct carcinoma colorectal cancer colorectal carcinoma cone-rod dystrophy 2 cone-rod dystrophy congenital toxoplasmosis congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma diabetes mellitus diabetic ketoacidosis distal myopathy embryoma endomyocardial fibrosis esophagus squamous cell carcinoma essential hypertension facioscapulohumeral muscular dystrophy follicular adenoma gastroenteritis glomerulonephritis granular cell carcinoma heart disease hepatocellular carcinoma hypertension ileitis ileocolitis juvenile rheumatoid arthritis kidney disease kidney hypertrophy large intestine cancer leech infestation limb-girdle muscular dystrophy liver cancer lymphoma malignant mesothelioma melanoma microcystic adenoma muscular dystrophy myeloproliferative neoplasm myiasis myocardial infarction nephritis nephrosis neuroblastoma neurodegenerative disease neuropathy nodular prostate nonpapillary renal cell carcinoma obesity 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 type 1 diabetes mellitus 9 obsolete ymphosarcoma oculopharyngeal muscular dystrophy osteoporosis ovarian cancer ovarian carcinoma papillary adenoma papillary renal cell carcinoma parapsoriasis peripheral nervous system disease pneumonia post-traumatic stress disorder prostate cancer prostate carcinoma prostatic adenoma psoriasis pustulosis of palm and sole pyoureter rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma retinal disease retinitis rheumatoid arthritis sarcomatoid renal cell carcinoma schizophrenia seborrheic keratosis silent myocardial infarction skin benign neoplasm skin cancer skin disease skin melanoma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma testicular cancer thyroid adenoma thyroid cancer thyroid gland carcinoma tongue squamous cell carcinoma toxoplasmosis tuberculosis 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 urinary bladder cancer vitelliform macular dystrophy vitiligo
9197	solute carrier family 33 member 1	SLC33A1 Aliases: AT-1 AT1 Acetyl-CoA transporter 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 Bartter disease Charcot-Marie-Tooth disease type 5 Conn's syndrome Henoch-Schoenlein purpura MASA syndrome Marfan syndrome Mast syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome SPOAN syndrome Troyer syndrome Waterhouse-Friderichsen syndrome abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 acute myocardial infarction adenocarcinoma adenoma adrenal gland cancer allergic asthma amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atrial fibrillation autism spectrum disorder autistic disorder bestrophinopathy brain disease brain ischemia brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiomyopathy cardiovascular system disease cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease chronic kidney disease colitis colorectal cancer colorectal carcinoma congenital nystagmus congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma deafness-dystonia-optic neuronopathy syndrome dementia depressive disorder diabetes mellitus diabetic ketoacidosis dissociated nystagmus dysthymic disorder embryoma endometriosis of uterus endometriosis endomyocardial fibrosis epilepsy epithelioid leiomyosarcoma essential hypertension familial hypertrophic cardiomyopathy focal epilepsy follicular adenoma gastroenteritis generalized anxiety disorder glomerulonephritis granular cell carcinoma heart disease hepatoblastoma hepatocellular carcinoma 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 hyperhomocysteinemia hypersensitivity vasculitis hypertension hypertensive heart disease hypertrophic cardiomyopathy ileitis ileocolitis intellectual disability intrinsic asthma kidney disease large intestine cancer learning disability leiomyosarcoma liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma major depressive disorder malignant hypertension melancholic depression melanoma microcystic adenoma myocardial infarction myxoid leiomyosarcoma nephritis nephrosis neurodegenerative disease neurotic disorder nodular prostate nutmeg liver obesity obsolete melancholia obstructive sleep apnea papillary adenoma paraplegia partial motor epilepsy pathologic nystagmus periodontitis phobic disorder placental insufficiency polycystic ovary syndrome primary hyperaldosteronism progressive muscular atrophy prostate cancer prostate carcinoma prostatic adenoma pyoureter renovascular hypertension scleroderma secondary hypertension sensorineural hearing loss sensory peripheral neuropathy sick sinus syndrome silent myocardial infarction situs inversus skin melanoma spontaneous ocular nystagmus systemic scleroderma trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis tubular adenocarcinoma type 2 diabetes mellitus vesicoureteral reflux visual epilepsy
51196	phospholipase C epsilon 1	PLCE1 Aliases: KIAA1516 NPHS3 PLCE nephrosis type 3 phosphoinositide phospholipase C	Homo sapiens (human)	46,XY sex reversal Alzheimer's disease Barrett's esophagus 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 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 3 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 Japanese encephalitis Miller-Dieker lissencephaly syndrome West Nile fever acute myeloid leukemia adenocarcinoma adenoma adenosarcoma agenesis of the corpus callosum with peripheral neuropathy atrophic gastritis bladder carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease chromosome 17p13.1 deletion syndrome chronic kidney disease chronic obstructive pulmonary disease colorectal cancer colorectal carcinoma common wart congestive heart failure cribriform carcinoma cytochrome-c oxidase deficiency disease dengue disease dengue hemorrhagic fever embryoma esophageal cancer esophageal carcinoma esophagitis esophagus adenocarcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia familial nephrotic syndrome focal segmental glomerulosclerosis gallbladder cancer gallbladder carcinoma gastric adenocarcinoma gastric cardia adenocarcinoma gastric cardia carcinoma gastritis gastroesophageal reflux disease gastrointestinal system cancer glomerulonephritis granular cell carcinoma head and neck squamous cell carcinoma heart disease hepatitis B hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hypertension large intestine cancer lipoid nephrosis lissencephaly liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma migraine mitochondrial metabolism disease motor peripheral neuropathy myelodysplastic syndrome nephritis nephroblastoma nephrotic syndrome type 1 nephrotic syndrome type 2 nephrotic syndrome type 3 nephrotic syndrome obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum open-angle glaucoma peptic esophagitis primary open angle glaucoma proteinuria sarcomatoid carcinoma squamous cell carcinoma squamous cell neoplasm stomach cancer stomach carcinoma temporal arteritis tongue squamous cell carcinoma tubular adenocarcinoma urinary bladder cancer viral infectious disease yellow fever
84513	phospholipid phosphatase 5	PLPP5 Aliases: DPPL1 HTPAP diacylglycerol pyrophosphate phosphatase-like 1	Homo sapiens (human)	breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer depressive disorder hepatocellular carcinoma liver cancer lung benign neoplasm lung cancer lung carcinoma lung small cell carcinoma major depressive disorder melancholic depression obsolete melancholia pancreatic adenocarcinoma
2582	UDP-galactose-4-epimerase	GALE Aliases: SDR1E1 UDP-glucose 4-epimerase short chain dehydrogenase/reductase family 1E, member 1	Homo sapiens (human)	Guillain-Barre syndrome Miller Fisher syndrome benign familial infantile epilepsy benign familial neonatal epilepsy benign neonatal seizures classic galactosemia cystinuria galactokinase deficiency galactose epimerase deficiency galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease stomach cancer stomach carcinoma thrombocytopenia tuberculosis

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