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 **126 - 150** of **1582** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
6487	ST3 beta-galactoside alpha-2,3-sialyltransferase 3	ST3GAL3 Aliases: N-acetyllactosaminide alpha-2,3-sialyltransferase ST3Gal III	Homo sapiens (human)	Unverricht-Lundborg syndrome West syndrome agnosia amyotrophic lateral sclerosis attention deficit hyperactivity disorder autosomal recessive intellectual developmental disorder 12 autosomal recessive intellectual developmental disorder bipolar disorder blepharospasm brain cancer breast cancer breast carcinoma cancer cerebral degeneration cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervix carcinoma choreatic disease congenital disorder of glycosylation depressive disorder developmental and epileptic encephalopathy 15 developmental coordination disorder diabetes mellitus dysthymic disorder dystonia early infantile epileptic encephalopathy early myoclonic encephalopathy embryoma epilepsy focal epilepsy focal hand dystonia hepatocellular carcinoma influenza intellectual disability learning disability lingual-facial-buccal dyskinesia liver cancer major depressive disorder melancholic depression microcephaly neurotic disorder obsolete infantile epileptic encephalopathy obsolete melancholia pancreatic adenocarcinoma partial motor epilepsy progressive muscular atrophy prostate cancer prostate carcinoma pterygium schizophrenia stereotypic movement disorder stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 type 2 diabetes mellitus visual epilepsy
8310	acyl-CoA oxidase 3, pristanoyl	ACOX3	Homo sapiens (human)	prostate cancer prostate carcinoma
1585	cytochrome P450 family 11 subfamily B member 2	CYP11B2 Aliases: ALDOS CPN2 CYP11BL P-450C18 P450aldo steroid 11-beta-monooxygenase	Homo sapiens (human)	46,XY sex reversal Bartter disease Conn's syndrome IgA glomerulonephritis Liddle syndrome Waterhouse-Friderichsen syndrome abdominal obesity-metabolic syndrome 1 acromegaly acute myocardial infarction adenocarcinoma adenoma adrenal adenoma adrenal carcinoma adrenal cortex cancer adrenal cortical adenoma adrenal gland cancer adrenal gland hyperfunction adrenocortical carcinoma aortic valve disease 2 aortic valve stenosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation 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 autism spectrum disorder autistic disorder brain infarction brain stem infarction cancer cardiomyopathy cardiovascular system disease carotid artery disease cerebral artery occlusion cerebral infarction cerebrovascular disease chronic kidney disease clear cell renal cell carcinoma congenital adrenal hyperplasia congenital central hypoventilation syndrome congestive heart failure coronary artery disease coronary thrombosis corticosterone methyloxidase deficiency 1 cribriform carcinoma diabetes mellitus diabetic ketoacidosis diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy 1H dilated cardiomyopathy disease of metabolism eclampsia embryoma endomyocardial fibrosis essential hypertension familial hypertrophic cardiomyopathy focal segmental glomerulosclerosis follicular adenoma glucocorticoid-remediable aldosteronism granular cell carcinoma heart disease hyperphosphatemia hyperpituitarism hypertension hypertensive heart disease hypertrophic cardiomyopathy hypokalemia kidney cancer kidney failure lactic acidosis microcystic adenoma multiple system atrophy myocardial infarction myocarditis nutmeg liver obsolete Cushing's syndrome papillary adenoma patent foramen ovale postural orthostatic tachycardia syndrome pre-eclampsia primary hyperaldosteronism prostate cancer prostate carcinoma psoriatic arthritis pulmonary edema relapsing fever renal carcinoma renal cell carcinoma renal tubular acidosis silent myocardial infarction trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tubular adenocarcinoma type 2 diabetes mellitus uremia
51006	solute carrier family 35 member C2	SLC35C2 Aliases: CGI-15 bA394O2.1	Homo sapiens (human)
114780	polycystin 1 like 2 (gene/pseudogene)	PKD1L2 Aliases: KIAA1879	Homo sapiens (human)	Meckel syndrome autosomal dominant polycystic kidney disease colorectal cancer colorectal carcinoma familial periodic paralysis hypoplastic left heart syndrome large intestine cancer myopathy neuromuscular disease
9955	heparan sulfate-glucosamine 3-sulfotransferase 3A1	HS3ST3A1 Aliases: 30ST3A1 3OST3A1	Homo sapiens (human)	breast cancer breast carcinoma
55454	chondroitin sulfate N-acetylgalactosaminyltransferase 2	CSGALNACT2 Aliases: GALNACT-2 GALNACT2 MGC40204 PRO0082 chondroitin beta1,4 N-acetylgalactosaminyltransferase 2 glucuronylgalactosylproteoglycan 4-beta-N-acetylgalactosaminyltransferase 2	Homo sapiens (human)	Hirschsprung's disease arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis multiple sclerosis
9572	nuclear receptor subfamily 1 group D member 1	NR1D1	Homo sapiens (human)	alcoholic liver cirrhosis brain small vessel disease hyperthyroidism hypothyroidism portal hypertension type 2 diabetes mellitus
4967	oxoglutarate dehydrogenase	OGDH Aliases: E1k KGD1 OGDC-E1 OGDH2	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 Laron syndrome Leigh disease Pick's disease Reye syndrome Yoon-Bellen neurodevelopmental syndrome achondroplasia alternating hemiplegia of childhood arteriosclerotic cardiovascular disease atherosclerosis autonomic neuropathy breast cancer cancer central nervous system disease cerebral degeneration colorectal cancer colorectal carcinoma communicating hydrocephalus congestive heart failure coronary artery disease embryoma hydrocephalus lactic acidosis large intestine cancer lingual-facial-buccal dyskinesia movement disease nervous system disease neuroblastoma neurodegenerative disease obstructive hydrocephalus oxoglutarate dehydrogenase deficiency phenylketonuria placental insufficiency primary biliary cholangitis pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency senile degeneration of brain status epilepticus urea cycle disorder viral infectious disease
5504	protein phosphatase 1 regulatory inhibitor subunit 2	PPP1R2	Homo sapiens (human)
4326	matrix metallopeptidase 17	MMP17 Aliases: MT4-MMP	Homo sapiens (human)	adenocarcinoma adenoma aortic aneurysm arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis breast adenocarcinoma breast cancer breast carcinoma cancer coronary artery disease cribriform carcinoma embryoma granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma migraine osteoporosis rheumatoid arthritis tubular adenocarcinoma
10941	UDP glucuronosyltransferase family 2 member A1 complex locus	UGT2A1	Homo sapiens (human)	cancer embryoma laryngeal disease ovarian cancer ovarian carcinoma tracheal disease
23509	protein O-fucosyltransferase 1	POFUT1 Aliases: FUT12 GDP-fucose protein O-fucosyltransferase 1 KIAA0180 O-FUT O-Fuc-T peptide-O-fucosyltransferase	Homo sapiens (human)	Dowling-Degos disease acrodermatitis actinic keratosis acute myocardial infarction bone marrow cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma chronic obstructive pulmonary disease colorectal cancer colorectal carcinoma congestive heart failure coronary artery anomaly coronary thrombosis dermatitis gallbladder disease hepatocellular carcinoma invasive ductal carcinoma large intestine cancer liver cancer liver disease lung benign neoplasm lung cancer lung carcinoma microcephaly myeloproliferative neoplasm myocardial infarction reticulate acropigmentation of Kitamura schizophrenia seborrheic keratosis silent myocardial infarction skin disease
5224	phosphoglycerate mutase 2	PGAM2 Aliases: PGAM-M	Homo sapiens (human)	Cockayne syndrome Cornelia de Lange syndrome D-bifunctional protein deficiency Dubowitz syndrome Greig cephalopolysyndactyly 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 Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome X-linked Aarskog syndrome autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome cancer carnitine palmitoyltransferase I deficiency chondrodysplasia-pseudohermaphroditism syndrome cystinuria disease of metabolism endometrial cancer endometrial carcinoma familial periodic paralysis galactosemia 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 isolated elevated serum creatine phosphokinase levels kidney failure microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II myoglobinuria myopathy prostate cancer prostate carcinoma pseudosarcomatous fibromatosis uterine corpus cancer
7165	TPD52 like 2	TPD52L2	Homo sapiens (human)
23193	glucosidase II alpha subunit	GANAB Aliases: G2AN GIIA GluII KIAA0088 neutral alpha-glucosidase AB	Homo sapiens (human)	Meckel syndrome arthritis arthropathy autosomal dominant polycystic kidney disease chronic fatigue syndrome encephalitis encephalomyelitis gallbladder disease liver disease multiple sclerosis myelitis osteoarthritis polycystic kidney disease 1 polycystic kidney disease 2 polycystic kidney disease 3 polycystic kidney disease polycystic liver disease
22914	killer cell lectin like receptor K1	KLRK1 Aliases: CD314 KLR NKG2-D NKG2D	Homo sapiens (human)	B-cell lymphoma Barrett's esophagus Behcet's disease Burkitt lymphoma Crohn's colitis Crohn's disease Ewing sarcoma Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Kaposi's sarcoma Kawasaki disease Langerhans-cell histiocytosis Sezary's disease X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia acute leukemia acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adult lymphoma alopecia alveolar echinococcosis anogenital venereal wart arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asbestosis ataxia telangiectasia atherosclerosis atypical chronic myeloid leukemia, BCR-ABL1 negative autoimmune disease autoimmune hepatitis autoimmune lymphoproliferative syndrome basal cell carcinoma benign deep fibrous histiocytoma benign mesothelioma bile duct adenocarcinoma bile duct carcinoma bone osteosarcoma breast cancer breast carcinoma bronchiolitis obliterans bronchiolitis bronchus cancer bronchus carcinoma byssinosis cancer carcinoma celiac disease central nervous system cancer cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood acute myeloid leukemia childhood leukemia childhood lymphoma childhood osteosarcoma cholangiocarcinoma chronic fatigue syndrome chronic monocytic leukemia chronic obstructive pulmonary disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma cutaneous fibrous histiocytoma diabetes mellitus diabetic ketoacidosis distal arthrogryposis embryoma encephalitis encephalomyelitis endometriosis of uterus endometriosis epithelioid sarcoma esophagus squamous cell carcinoma familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperlipidemia familial retinoblastoma fibrosarcoma gallbladder disease gastrointestinal system cancer giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hepatitis A hepatitis B hepatitis C hepatitis hepatocellular carcinoma high grade glioma histiocytoma hyperglycemia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis immune system disease inflammatory bowel disease 1 inflammatory bowel disease intrahepatic cholangiocarcinoma islet cell tumor large intestine cancer leukemia leukocyte adhesion deficiency 1 leukocyte adhesion deficiency liver cancer liver carcinoma liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus erythematosus lymphoblastic lymphoma lymphoid leukemia lymphoma lymphoproliferative syndrome malignant mesothelioma melanoma mixed glioma monoclonal gammopathy of uncertain significance monocytic leukemia multiple myeloma multiple sclerosis myelitis myeloid leukemia myocardial infarction myocarditis nasopharynx carcinoma neuroblastoma non-Hodgkin lymphoma obsolete ymphosarcoma osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancytopenia paroxysmal nocturnal hemoglobinuria primary sclerosing cholangitis prolactinoma prostate cancer prostate carcinoma refractory plasma cell neoplasm reticulohistiocytic granuloma reticulosarcoma retinoblastoma rheumatoid arthritis sarcoma sclerosing cholangitis sclerosing hemangioma sebaceous carcinoma silent myocardial infarction skin melanoma spindle cell sarcoma spondyloarthropathy spondylosis squamous cell carcinoma squamous cell neoplasm stomach cancer stomach carcinoma sweat gland cancer systemic lupus erythematosus temporal arteritis thyroid gland anaplastic carcinoma tongue squamous cell carcinoma trilateral retinoblastoma tropical spastic paraparesis tuberculosis tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis viral infectious disease
4907	5'-nucleotidase ecto	NT5E Aliases: CALJA CD73 eN eNT	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 Baraitser-Winter syndrome Chagas disease Crohn's colitis Crohn's disease Down syndrome Fabry disease Fraser syndrome 1 Fraser syndrome Gilbert syndrome Goldenhar syndrome Goodpasture syndrome Graves' disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Jervell-Lange Nielsen syndrome Kallmann syndrome MHC class II deficiency Meniere's disease Moebius syndrome Muckle-Wells syndrome Muenke Syndrome Nance-Horan syndrome Oliver-McFarlane syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome Sakati-Nyhan syndrome Sheehan syndrome Takayasu's arteritis Troyer syndrome Turner syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome X-linked agammaglobulinemia acinar cell carcinoma acoustic neuroma acute lymphoblastic leukemia acute maxillary sinusitis acute monocytic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adenosine deaminase deficiency adult acute lymphocytic leukemia adult epithelioid sarcoma adult lymphoma adult medulloblastoma adult respiratory distress syndrome agammaglobulinemia allergic asthma allergic rhinitis amnestic disorder amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 angiomatous meningioma angle-closure glaucoma ankylosing spondylitis anterior horn cell disease anxiety disorder aortic valve disease 1 aortic valve disease 2 aortic valve disease aortic valve stenosis arterial calcification of infancy arterial tortuosity syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome autoimmune polyendocrine syndrome autoimmune thyroiditis autosomal recessive distal hereditary motor neuronopathy 1 basal cell carcinoma benign meningioma benign mesothelioma bicuspid aortic valve disease bile duct adenocarcinoma bile duct carcinoma bilirubin metabolic disorder bladder carcinoma brain cancer branchiootic syndrome breast cancer breast carcinoma bronchus cancer bronchus carcinoma calciphylaxis cancer carcinoma cardiac arrest cardiovascular system disease cecum adenocarcinoma celiac disease central nervous system cancer central nervous system origin vertigo cerebral convexity meningioma cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood acute lymphocytic leukemia childhood epithelioid sarcoma childhood leukemia childhood lymphoma childhood medulloblastoma cholangiocarcinoma cholera chromophobe renal cell carcinoma chronic closed-angle glaucoma chronic fatigue syndrome chronic lymphocytic leukemia chronic maxillary sinusitis chronic obstructive pulmonary disease chronic rhinitis chylomicron retention disease clear cell meningioma clear cell renal cell carcinoma cleft palate colitis collagen disease collecting duct carcinoma colorectal cancer colorectal carcinoma common wart communicating hydrocephalus congenital hemolytic anemia congenital hypogammaglobulinemia congenital nystagmus congestive heart failure connective tissue disease corneal disease coronary artery disease coronary thrombosis craniosynostosis cribriform carcinoma depressive disorder diffuse large B-cell lymphoma dissociated nystagmus double outlet right ventricle dysthymic disorder embryoma encephalitis encephalomyelitis endolymphatic hydrops endometrial cancer endometrial carcinoma endometriosis of ovary endometriosis enthesopathy epilepsy esophagitis esophagus squamous cell carcinoma eunuchism fibromyalgia fibrous meningioma gallbladder adenocarcinoma gallbladder cancer gallbladder carcinoma gastritis gastroenteritis gastroesophageal reflux disease generalized anxiety disorder giant cell glioblastoma glioblastoma gliosarcoma gonadal dysgenesis granular cell carcinoma granulomatosis with polyangiitis head and neck cancer head and neck squamous cell carcinoma heart disease hemoglobin C disease hemoglobin D disease hemoglobin E disease hemoglobinopathy hepatitis hepatocellular carcinoma hereditary arterial and articular multiple calcification syndrome high grade glioma hydrocephalus hyperthyroidism 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 idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome immune system disease inflammatory bowel disease 1 inflammatory bowel disease intrahepatic cholangiocarcinoma intraorbital meningioma intraventricular meningioma intrinsic asthma isolated cleft palate 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 keratoconus keratosis follicularis kidney cancer large intestine cancer laryngeal disease laryngeal squamous cell carcinoma lateral sclerosis lipid storage disease liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus erythematosus lymphoblastic lymphoma major depressive disorder malignant mesothelioma mastoiditis maxillary sinusitis medulloblastoma medullomyoblastoma melancholic depression melanoma melanotic medulloblastoma meningioma meningothelial meningioma microcystic meningioma microphthalmia mixed glioma mongolian spot motor neuron disease mucocele of salivary gland mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis multiple sclerosis myelitis myocardial infarction neuroblastoma neuroendocrine carcinoma neuroendocrine tumor neuropathy neurotic disorder newborn respiratory distress syndrome non-suppurative otitis media nonpapillary renal cell carcinoma nutmeg liver obsolete Matthew-Wood syndrome obsolete melancholia obstructive hydrocephalus obstructive sleep apnea olfactory groove meningioma orofaciodigital syndrome I orofaciodigital syndrome X osteoarthritis otitis media ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma panhypopituitarism papillary adenocarcinoma papillary renal cell carcinoma parapsoriasis parasagittal meningioma pathologic nystagmus peptic esophagitis pericarditis periodontitis peripheral nervous system disease peripheral vascular disease pituitary adenoma polyarteritis nodosa polyneuropathy postinflammatory pulmonary fibrosis primary angle-closure glaucoma primary ciliary dyskinesia 1 primary ciliary dyskinesia primary immunodeficiency disease prostate cancer prostate carcinoma psammomatous meningioma pseudoxanthoma elasticum psoriasis pulmonary fibrosis pustulosis of palm and sole pycnodysostosis rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma renal osteodystrophy retrograde amnesia rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma secretory meningioma senile degeneration of brain sensorineural hearing loss septooptic dysplasia severe combined immunodeficiency sickle cell anemia silent myocardial infarction skin melanoma spinal meningioma spontaneous ocular nystagmus squamous cell carcinoma status epilepticus stomach cancer stomach carcinoma suppurative periapical periodontitis thrombophilia thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma tonsillitis tracheal disease transitional meningioma trypanosomiasis tuberculosis tubular adenocarcinoma ulcerative colitis urinary bladder cancer uterine corpus cancer vasculitis vasomotor rhinitis visual epilepsy
54988	acyl-CoA synthetase medium chain family member 5	ACSM5 Aliases: FLJ20581	Homo sapiens (human)
4594	methylmalonyl-CoA mutase	MMUT Aliases: MCM	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 Kallmann syndrome Pick's disease Reye syndrome Sheehan syndrome acoustic neuroma actinic keratosis acute pancreatitis adult medulloblastoma adult oligodendroglioma agranulocytosis ampulla of Vater carcinoma anemia angiomatous meningioma 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 bacterial sepsis basal cell carcinoma basal ganglia disease benign meningioma blepharospasm bone osteosarcoma branched-chain keto acid dehydrogenase kinase deficiency breast cancer bronchus cancer bronchus carcinoma bulbar polio cancer cardiomyopathy cataract 40 central nervous system cancer cerebral convexity meningioma cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix disease cervix uteri carcinoma in situ childhood medulloblastoma childhood oligodendroglioma childhood osteosarcoma chromophobe renal cell carcinoma clear cell meningioma clear cell renal cell carcinoma collecting duct carcinoma colon carcinoma colorectal cancer colorectal carcinoma congestive heart failure conversion disorder diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dissociative disorder dystonia embryoma endomyocardial fibrosis epilepsy familial retinoblastoma fibrous meningioma focal hand dystonia giant cell glioblastoma glioblastoma gliosarcoma hepatocellular carcinoma high grade glioma homocystinuria hypertrophic cardiomyopathy 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 in situ carcinoma influenza inherited metabolic disorder intellectual disability interstitial nephritis intraorbital meningioma intraventricular meningioma inverted follicular keratosis 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 keratoacanthoma kidney failure large intestine cancer laryngeal squamous cell carcinoma learning disability leukopenia liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma macrocytic anemia mal de Meleda medulloblastoma medullomyoblastoma melanoacanthoma melanotic medulloblastoma meningioma meningothelial meningioma methylmalonic acidemia cblA type methylmalonic acidemia cblB type methylmalonic acidemia due to transcobalamin receptor defect methylmalonic acidemia methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency microcystic meningioma microphthalmia mitochondrial metabolism disease mixed glioma mixed oligodendroglioma-astrocytoma nasopharynx carcinoma neuroblastoma neutropenia nonpapillary renal cell carcinoma obesity obsolete Matthew-Wood syndrome olfactory groove meningioma oligodendroglioma optic atrophy osteosarcoma palmoplantar keratosis pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma pancreatitis pancytopenia panhypopituitarism papillary adenocarcinoma papillary renal cell carcinoma parasagittal meningioma patent foramen ovale penis carcinoma in situ pituitary adenoma poliomyelitis primary immunodeficiency disease propionic acidemia psammomatous meningioma pyelonephritis renal carcinoma renal cell carcinoma renal infectious disease retinoblastoma sarcomatoid renal cell carcinoma seborrheic keratosis secretory meningioma severe congenital neutropenia skin disease skin squamous cell carcinoma spinal meningioma stomach cancer stomach carcinoma syndactyly thrombocytopenia thyroid gland anaplastic carcinoma thyroid gland papillary carcinoma transcobalamin II deficiency transitional cell carcinoma transitional meningioma trilateral retinoblastoma tropical sprue tuberculosis urea cycle disorder visual epilepsy
2729	glutamate-cysteine ligase catalytic subunit	GCLC	Homo sapiens (human)	cataract colorectal cancer cystic fibrosis glutamate-cysteine ligase deficiency hemolytic anemia liver cirrhosis myocardial infarction pulmonary emphysema
23213	sulfatase 1	SULF1 Aliases: Extracellular sulfatase Sulf-1 KIAA1077 SULF-1 hSulf-1	Homo sapiens (human)	Marinesco-Sjogren syndrome acute pancreatitis adult hepatocellular carcinoma anal carcinoma in situ arthritis arthropathy bacterial sepsis bladder urothelial carcinoma brain cancer breast cancer breast carcinoma breast ductal carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cervix uteri carcinoma in situ childhood hepatocellular carcinoma colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma degenerative disc disease disease of metabolism embryoma giant cell glioblastoma glioblastoma head and neck squamous cell carcinoma hepatitis hepatocellular carcinoma high grade glioma idiopathic interstitial pneumonia large intestine cancer liver cancer liver carcinoma liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma melanoma nodular prostate osteoarthritis ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatitis pneumonia postinflammatory pulmonary fibrosis primary cerebellar degeneration prostatic adenoma pulmonary fibrosis seminoma skin melanoma steatotic liver disease stomach cancer stomach carcinoma testicular cancer testis seminoma transitional cell carcinoma
152831	klotho beta	KLB Aliases: b-Klotho	Homo sapiens (human)	Clostridium difficile colitis allergic rhinitis autosomal dominant hypophosphatemic rickets breast cancer breast carcinoma cancer cartilage-hair hypoplasia diabetes mellitus diabetic ketoacidosis diarrhea disease of metabolism embryoma familial hyperlipidemia gestational diabetes hepatocellular carcinoma intrahepatic cholestasis of pregnancy invasive ductal carcinoma irritable bowel syndrome kidney disease kidney failure liver cancer lung cancer lung non-small cell carcinoma neurocirculatory asthenia nodular prostate obesity ovarian disease papillary adenocarcinoma papillary renal cell carcinoma prostate cancer prostate carcinoma prostatic adenoma steatotic liver disease thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma thyroid gland follicular carcinoma thyroid gland papillary carcinoma type 2 diabetes mellitus uremia vasomotor rhinitis
1103	choline O-acetyltransferase	CHAT	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 Balo concentric sclerosis Down syndrome Gilles de la Tourette syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Lambert-Eaton myasthenic syndrome Marfan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Rett syndrome Reye syndrome X-linked adrenal hypoplasia congenita acute myocardial infarction adrenoleukodystrophy agnosia allergic asthma amnestic disorder amyloidosis angle-closure glaucoma arthritis arthropathy aspiration pneumonia aspiration pneumonitis asthma atrial fibrillation autism spectrum disorder autistic disorder beriberi bronchus cancer bronchus carcinoma bulbar polio cancer cannabis abuse cannabis dependence central nervous system disease central sleep apnea centronuclear myopathy cerebral degeneration cerebral infarction cerebrovascular disease chronic closed-angle glaucoma chronic fatigue syndrome clubfoot colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital myasthenic syndrome 21 congenital myasthenic syndrome 6 congenital myasthenic syndrome congenital nystagmus congenital ptosis congenital structural myopathy coronary thrombosis critical illness polyneuropathy dementia depressive disorder developmental coordination disorder diabetes mellitus diabetic ketoacidosis differentiating neuroblastoma disease of mental health dissociated nystagmus dry beriberi dysthymic disorder encephalitis encephalomyelitis epilepsy esophagitis esotropia focal epilepsy gastroesophageal reflux disease gastroparesis giant cell glioblastoma glioblastoma hypertropia hypoglycemia idiopathic interstitial pneumonia intellectual disability intrinsic asthma kernicterus due to isoimmunization kernicterus lactic acidosis large intestine cancer learning disability lung benign neoplasm lung cancer lung carcinoma lymphocytic choriomeningitis major depressive disorder mechanical strabismus melancholic depression middle cerebral artery infarction monocular esotropia mucopolysaccharidosis III mucopolysaccharidosis type IIIA multiple sclerosis myelitis myocardial infarction narcolepsy nervous system disease neuroblastoma neurodegenerative disease neuromuscular disease neurotic disorder nicotine dependence obsolete constipation obsolete melancholia obsolete type 1 diabetes mellitus 9 obstructive sleep apnea olivopontocerebellar atrophy ophthalmoplegia osteoarthritis partial motor epilepsy pathologic nystagmus pellagra peptic esophagitis poliomyelitis polyhydramnios polyneuropathy postinflammatory pulmonary fibrosis primary angle-closure glaucoma progressive bulbar palsy psychotic disorder ptosis pulmonary fibrosis red-green color blindness retinal disease retinitis retrograde amnesia rheumatoid arthritis schizophrenia scoliosis secondary Parkinson disease sensorineural hearing loss silent myocardial infarction situs inversus spontaneous ocular nystagmus stereotypic movement disorder strabismus sudden infant death syndrome tendinitis thiamine deficiency disease 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 type 2 diabetes mellitus vascular dementia visual epilepsy
8869	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	ST3GAL5 Aliases: SIATGM3S ST3GalV ganglioside GM3 synthase lactosylceramide alpha-2,3-sialyltransferase	Homo sapiens (human)	Charcot-Marie-Tooth disease type 5 MASA syndrome Mast syndrome Niemann-Pick disease type C1 Niemann-Pick disease Rett syndrome SPOAN syndrome Troyer syndrome Unverricht-Lundborg syndrome agnosia arthritis arthropathy blepharospasm blindness cerebral palsy congenital nystagmus developmental and epileptic encephalopathy 36 dissociated nystagmus dystonia early myoclonic encephalopathy endocrine exophthalmos focal hand dystonia hemiplegia 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 intellectual disability learning disability lingual-facial-buccal dyskinesia liver cancer locked-in syndrome microcephaly optic atrophy paroxysmal nonkinesigenic dyskinesia 1 paroxysmal nonkinesigenic dyskinesia 2 pathologic nystagmus quadriplegia salt and pepper syndrome sensorineural hearing loss spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spontaneous ocular nystagmus status epilepticus stereotypic movement disorder syndromic X-linked intellectual disability 94 thromboangiitis obliterans trichohepatoenteric syndrome 1 trichohepatoenteric syndrome visual epilepsy

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