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 **392726 - 392750** of **393515** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
9562	multiple inositol-polyphosphate phosphatase 1	MINPP1 Aliases: MIPP	Homo sapiens (human)	actinic keratosis cancer carcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colonic benign neoplasm colorectal cancer head and neck cancer large intestine cancer multiple myeloma nodular goiter papillary adenocarcinoma papillary renal cell carcinoma pontocerebellar hypoplasia type 16 renal cell carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma seborrheic keratosis skin disease spinal cord disease thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma thyroid gland papillary carcinoma
9536	prostaglandin E synthase	PTGES Aliases: MGST-IV MGST1-L1 MGST1-like 1 PIG12 TP53I12 glutathione S-transferase 1-like 1 microsomal glutathione S-transferase 1-like 1 microsomal prostaglandin E synthase-1 p53-induced gene 12 tumor protein p53 inducible protein 12	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 Hirschsprung's disease Leydig cell tumor Marinesco-Sjogren syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome T-cell acute lymphoblastic leukemia abdominal aortic aneurysm acute myocardial infarction adenocarcinoma adenoma adult lymphoma allergic asthma amyotrophic lateral sclerosis anaplastic astrocytoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis autism spectrum disorder autistic disorder bile duct adenocarcinoma bile duct carcinoma brain disease breast cancer breast carcinoma breast disease bronchus cancer bronchus carcinoma cancer carcinoma carotid artery disease central nervous system cancer central nervous system lymphoma cerebral degeneration cerebral infarction cerebrovascular disease childhood cerebral astrocytoma childhood lymphoma cholangiocarcinoma chronic fatigue syndrome chronic kidney disease colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis cribriform carcinoma disease of metabolism distal arthrogryposis ductal carcinoma in situ embryoma encephalitis encephalomyelitis endometrial adenocarcinoma endometriosis of uterus endometriosis epilepsy esophageal cancer esophageal carcinoma esophagitis esophagus adenocarcinoma esophagus squamous cell carcinoma essential hypertension familial adenomatous polyposis 1 familial adenomatous polyposis fibrillary astrocytoma gastroenteritis gastroesophageal reflux disease gemistocytic astrocytoma gliosarcoma glomerulonephritis granular cell carcinoma head and neck squamous cell carcinoma hepatitis A hepatitis B hepatitis hepatocellular carcinoma high grade glioma hydronephrosis hypertension ileitis ileocolitis ileus in situ carcinoma inflammatory bowel disease intestinal obstruction intracranial aneurysm intrahepatic cholangiocarcinoma intrinsic asthma ischemia islet cell tumor isovaleric acidemia juvenile pilocytic astrocytoma kidney disease lactocele large intestine cancer liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma malignant astrocytoma melanoma mixed glioma multiple sclerosis myelitis myocardial infarction nephritis nephrosis neuroblastoma neurodegenerative disease obesity obsolete ymphosarcoma osteoarthritis ovary epithelial cancer pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary renal cell carcinoma papilloma patent ductus arteriosus penile benign neoplasm peptic esophagitis periodontitis pilocytic astrocytoma pneumonia primary cerebellar degeneration primary ovarian insufficiency primary sclerosing cholangitis progressive muscular atrophy prostate cancer prostate carcinoma protoplasmic astrocytoma pyoureter rheumatoid arthritis sarcomatoid carcinoma sclerosing cholangitis silent myocardial infarction skin benign neoplasm skin cancer skin melanoma squamous cell carcinoma squamous cell papilloma squamous papillomatosis status epilepticus subependymal giant cell astrocytoma thymic carcinoma thymoma thyroid gland papillary carcinoma tongue squamous cell carcinoma transitional cell carcinoma tubular adenocarcinoma type C thymoma ureteral obstruction visual epilepsy
9526	mannose-P-dolichol utilization defect 1	MPDU1 Aliases: CDGIf Lec35 PQLC5 SL15 SLC66A5	Homo sapiens (human)	IgA glomerulonephritis acquired hyperkeratosis autosomal recessive congenital ichthyosis 1 blindness cancer cerebral degeneration congenital disorder of glycosylation Id congenital disorder of glycosylation If congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital disorder of glycosylation congenital hypothyroidism congenital nystagmus craniosynostosis cystinuria dissociated nystagmus galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease hypertropia hypothyroidism ichthyosis keratosis follicularis mechanical strabismus microcephaly mongolian spot myxedema obsolete congenital ichthyosiform erythroderma ophthalmoplegia optic atrophy pathologic nystagmus pseudoxanthoma elasticum spontaneous ocular nystagmus strabismus
9524	trans-2,3-enoyl-CoA reductase	TECR Aliases: MRT14 TER very-long-chain enoyl-CoA reductase	Homo sapiens (human)	Marfan syndrome agnosia autosomal recessive intellectual developmental disorder 14 autosomal recessive intellectual developmental disorder cardiovascular system disease cerebral degeneration choreatic disease depressive disorder developmental coordination disorder dyskeratosis congenita dysthymic disorder dystonia endometriosis of uterus endometriosis epilepsy focal epilepsy heart disease influenza intellectual disability learning disability lingual-facial-buccal dyskinesia major depressive disorder melancholic depression microcephaly neurotic disorder non-syndromic intellectual disability obsolete infantile epileptic encephalopathy obsolete melancholia partial motor epilepsy pneumothorax situs inversus stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 tuberous sclerosis visual epilepsy
9517	serine palmitoyltransferase long chain base subunit 2	SPTLC2 Aliases: KIAA0526 LCB2 LCB2A hLCB2a	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 acute myocardial infarction agenesis of the corpus callosum with peripheral neuropathy anhidrosis cancer coronary thrombosis diarrhea hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 1 hereditary sensory and autonomic neuropathy type 1A hereditary sensory and autonomic neuropathy type 1C hereditary sensory and autonomic neuropathy type 2 hereditary sensory neuropathy hypohidrosis liver cancer motor peripheral neuropathy myocardial infarction neuropathy obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum osteomyelitis parapsoriasis peripheral nervous system disease psoriasis pustulosis of palm and sole sensory peripheral neuropathy silent myocardial infarction teratocarcinoma
9514	galactose-3-O-sulfotransferase 1	GAL3ST1 Aliases: CST cerebroside (3' phosphoadenylylsulfate:galactosylceramide 3') sulfotransferase	Homo sapiens (human)	Behcet's disease Marfan syndrome Papillon-Lefevre disease acute myocardial infarction adenocarcinoma adenoma amyotrophic lateral sclerosis anhidrosis anterior horn cell disease arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis brain stem infarction breast cancer breast carcinoma cancer cardiovascular system disease central nervous system cancer cerebral artery occlusion cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma cone-rod dystrophy 2 cone-rod dystrophy congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma diabetes mellitus diabetic ketoacidosis diabetic macular edema embryoma episodic kinesigenic dyskinesia 1 essential hypertension gliosarcoma granular cell carcinoma heart disease hepatitis B hepatocellular carcinoma high grade glioma hyperglycemia hypertension hypohidrosis immune system disease inflammatory bowel disease 1 inflammatory bowel disease influenza invasive ductal carcinoma lateral sclerosis liver cancer mixed glioma motor neuron disease myocardial infarction myotonic dystrophy type 2 nonpapillary renal cell carcinoma obesity obsolete type 1 diabetes mellitus 9 osteoarthritis papillary renal cell carcinoma progressive bulbar palsy progressive muscular atrophy renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction situs inversus stomach cancer stomach carcinoma substance abuse substance-related disorder tuberous sclerosis 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
9489	phosphatidylglycerophosphate synthase 1	PGS1 Aliases: DKFZP762M186	Homo sapiens (human)	acute myeloid leukemia
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
9487	phosphatidylinositol glycan anchor biosynthesis class L	PIGL Aliases: N-acetylglucosaminyl-phosphatidylinositol de-N-acetylase N-acetylglucosaminylphosphatidylinositol deacetylase PIG-L	Homo sapiens (human)	CAKUT2 CHIME syndrome Cogan syndrome Hailey-Hailey disease Hirschsprung's disease Rothmund-Thomson syndrome T-cell acute lymphoblastic leukemia Unverricht-Lundborg syndrome acquired hyperkeratosis acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia amyotrophic lateral sclerosis anodontia autistic disorder autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa 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 blepharospasm capillary disease cerebral degeneration chronic ulcer of skin cleft palate coloboma congenital ptosis craniosynostosis cutis laxa dextro-looped transposition of the great arteries diffuse interstitial keratitis disease of mental health early myoclonic encephalopathy epilepsy esotropia focal hand dystonia granuloma annulare hereditary hemorrhagic telangiectasia hydronephrosis hyperopia hypertropia hypotrichosis ichthyosis intellectual disability isolated cleft palate learning disability lymphoblastic lymphoma mal de Meleda mechanical strabismus monocular esotropia multiple types of congenital heart defects 6 nonepidermolytic palmoplantar keratoderma obsolete dextro-looped transposition of the great arteries 1 oligohydramnios ophthalmoplegia palmoplantar keratosis progressive muscular atrophy psychotic disorder ptosis recurrent corneal erosion restrictive dermopathy scoliosis sensorineural hearing loss strabismus syndromic X-linked intellectual disability 94 telangiectasis tetralogy of Fallot tooth agenesis ventricular septal defect visual epilepsy
9486	carbohydrate sulfotransferase 10	CHST10 Aliases: HNK-1ST	Homo sapiens (human)	Japanese encephalitis dengue disease schizophrenia viral infectious disease yellow fever
9469	carbohydrate sulfotransferase 3	CHST3 Aliases: C6ST C6ST1 chondroitin 6 sulfotransferase 1	Homo sapiens (human)	Bannayan-Riley-Ruvalcaba syndrome Bartter disease Conn's syndrome Cowden syndrome Desbuquois dysplasia Hailey-Hailey disease Laron syndrome Larsen syndrome Larsen-like syndrome B3GAT3 type Ollier disease Rothmund-Thomson syndrome SOST-related sclerosing bone dysplasia Schwartz-Jampel syndrome 1 Silverman-Handmaker type dyssegmental dysplasia Sjogren's syndrome Waterhouse-Friderichsen syndrome X-linked spondyloepiphyseal dysplasia tarda achondroplasia acute promyelocytic leukemia adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenal gland cancer adrenocortical carcinoma adrenoleukodystrophy adult fibrosarcoma agnosia alcoholic hepatitis alcoholic liver cirrhosis amblyopia aortic valve disease 1 aortic valve disease 2 aortic valve insufficiency aortic valve stenosis apparent mineralocorticoid excess syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atopic dermatitis 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 atrophy of testis autoimmune hepatitis autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa 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 bicuspid aortic valve disease blastomycosis breast cancer breast carcinoma buphthalmos cancer cardiomyopathy cardiovascular system disease choriocarcinoma cleft palate cleidocranial dysplasia clubfoot communicating hydrocephalus congenital adrenal hyperplasia coronary artery disease craniosynostosis cutis laxa cystadenoma dermatitis developmental coordination disorder diabetes mellitus diabetic ketoacidosis diastrophic dysplasia embryoma endometrial adenocarcinoma endometrial cancer endometrial carcinoma endometrial hyperplasia endometriosis of uterus endometriosis endomyocardial fibrosis enterocele esotropia essential hypertension fibrosarcoma follicular adenoma heart disease hepatitis hereditary multiple exostoses humeroradial synostosis hydrocephalus hydrophthalmos hyperopia hypertension hypertrophic cardiomyopathy hypogonadotropic hypogonadism 23 with or without anosmia inclusion body myositis intrahepatic cholestasis isolated cleft palate juvenile glaucoma keratoconjunctivitis sicca leiomyoma liver cirrhosis lung small cell carcinoma mal de Meleda microcystic adenoma mitral valve insufficiency mitral valve prolapse mitral valve stenosis monocular esotropia mucopolysaccharidosis IV multiple epiphyseal dysplasia myofibroma neurogenic arthropathy obesity obsolete type 1 diabetes mellitus 9 obstructive hydrocephalus osteochondrodysplasia osteoporosis ovarian cancer ovarian carcinoma ovarian hyperstimulation syndrome papillary adenoma paracoccidioidomycosis patent foramen ovale placenta cancer polycystic ovary syndrome postural orthostatic tachycardia syndrome primary hyperaldosteronism primary pulmonary hypertension progressive familial intrahepatic cholestasis progressive pseudorheumatoid arthropathy of childhood pulmonary valve stenosis radioulnar synostosis restrictive dermopathy rheumatoid arthritis schizophrenia scoliosis senile degeneration of brain sensorineural hearing loss spondyloepiphyseal dysplasia congenita spondyloepiphyseal dysplasia with congenital joint dislocations strabismic amblyopia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tricuspid valve insufficiency tricuspid valve stenosis 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 uterine corpus cancer uterine fibroid varicose veins ventricular septal defect
9468	phosphate cytidylyltransferase 1B, choline	PCYT1B Aliases: CCT-beta CCTbeta CTB CTP:phosphocholine cytidylyltransferase-beta choline-phosphate cytidylyltransferase beta phosphorylcholine transferase beta	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 Leber congenital amaurosis 1 Pick's disease Reye syndrome adult respiratory distress syndrome allergic rhinitis amyotrophic lateral sclerosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis breast cancer breast carcinoma breast ductal carcinoma cancer cerebral degeneration cholera colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary artery disease diabetes mellitus diabetic ketoacidosis embryoma hepatocellular carcinoma inflammatory bowel disease 1 inflammatory bowel disease juvenile rheumatoid arthritis large intestine cancer liver cancer liver carcinoma newborn respiratory distress syndrome progressive muscular atrophy prostate cancer prostate carcinoma type 2 diabetes mellitus ulcerative colitis urinary tract obstruction vasomotor rhinitis
9446	glutathione S-transferase omega 1	GSTO1	Homo sapiens (human)	Alzheimer's disease Parkinson's disease alcohol use disorder
9435	carbohydrate sulfotransferase 2	CHST2 Aliases: C6ST	Homo sapiens (human)	amyotrophic lateral sclerosis bone osteosarcoma cancer extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue gastric lymphoma inflammatory bowel disease 1 inflammatory bowel disease osteosarcoma progressive muscular atrophy ulcerative colitis
9420	cytochrome P450 family 7 subfamily B member 1	CYP7B1	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 Charcot-Marie-Tooth disease type 5 Henoch-Schoenlein purpura MASA syndrome Mast syndrome Pick's disease Reye syndrome SPOAN syndrome Troyer syndrome acquired immunodeficiency syndrome adenocarcinoma adenoma arthritis arthropathy autosomal recessive polycystic kidney disease blood coagulation disease breast cancer breast carcinoma cancer cataract cerebellar ataxia cerebellar disease cerebral degeneration cholestasis chronic obstructive pulmonary disease colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital bile acid synthesis defect 3 congenital bile acid synthesis defect congenital nystagmus cribriform carcinoma critical illness polyneuropathy depressive disorder diabetes mellitus diabetic ketoacidosis diarrhea disease of metabolism dissociated nystagmus embryoma gallbladder cancer gallbladder carcinoma gallbladder disease gastroenteritis granular cell carcinoma hepatitis 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 hypersensitivity vasculitis ileitis ileocolitis inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease intrahepatic cholestasis kwashiorkor large intestine cancer lipid metabolism disorder liver disease luminal breast carcinoma A major depressive disorder marasmus melancholic depression meningoencephalitis multiple sclerosis neurodegenerative disease neuropathy nutrition disease obsolete inherited blood coagulation disease obsolete melancholia obsolete steatorrhea optic atrophy osteoarthritis paraplegia pathologic nystagmus peripheral nervous system disease polycystic kidney disease 4 polyneuropathy prostate adenocarcinoma prostate cancer prostate carcinoma protein-energy malnutrition rheumatoid arthritis scoliosis sensorineural hearing loss spontaneous ocular nystagmus steatotic liver disease tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis
9415	fatty acid desaturase 2	FADS2 Aliases: D6D DES6 FADSD6 SLL0262 TU13 delta-6-desaturase	Homo sapiens (human)	Crohn's colitis Crohn's disease Fabry disease Wolman disease abdominal obesity-metabolic syndrome 1 acquired immunodeficiency syndrome acute myocardial infarction age related macular degeneration alcohol use disorder allergic asthma alopecia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atopic dermatitis atrial fibrillation attention deficit hyperactivity disorder autism spectrum disorder autistic disorder bipolar I disorder bipolar disorder breast cancer breast carcinoma cancer cardiovascular system disease cerebral infarction cerebrovascular disease chronic kidney disease chylomicron retention disease colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma congenital hypothyroidism congestive heart failure coronary artery disease coronary thrombosis degeneration of macula and posterior pole depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy discrete subaortic stenosis embryoma giant cell glioblastoma glioblastoma glomerulonephritis heart disease hemochromatosis type 1 hemochromatosis hepatitis hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease hypothyroidism inflammatory bowel disease 1 inflammatory bowel disease intrinsic asthma kidney disease kwashiorkor large intestine cancer laryngeal squamous cell carcinoma lipid metabolism disorder lipid storage disease liver cancer lung benign neoplasm lung carcinoma macular degeneration major depressive disorder marasmus melancholic depression myocardial infarction myxedema nephritis nephrosis neurotic disorder nutmeg liver nutrition disease obesity obsolete melancholia polycystic ovary syndrome progressive pseudorheumatoid arthropathy of childhood protein-energy malnutrition psoriatic arthritis pyoureter rheumatoid arthritis schizophrenia silent myocardial infarction skin disease steatotic liver disease stomach cancer stomach carcinoma type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis vitiligo
9394	heparan sulfate 6-O-sulfotransferase 1	HS6ST1	Homo sapiens (human)	Kallmann syndrome Potter's syndrome Sheehan syndrome achromatopsia acquired color blindness anxiety disorder bilateral renal aplasia blindness blue color blindness cartilage-hair hypoplasia clubfoot color blindness congenital nystagmus congenital ptosis cryptorchidism depressive disorder diabetes mellitus diabetic ketoacidosis dissociated nystagmus dysthymic disorder epilepsy eunuchism generalized anxiety disorder gynecomastia hypertrophy of breast 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 15 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 idiopathic interstitial pneumonia idiopathic pulmonary fibrosis impotence infant gynecomastia 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 major depressive disorder melancholic depression mucopolysaccharidosis IV multiple epiphyseal dysplasia neurotic disorder obesity obsolete melancholia osteochondrodysplasia osteoporosis panhypopituitarism paraplegia pathologic nystagmus premature ejaculation psychologic dyspareunia ptosis red color blindness red-green color blindness schizophrenia sensorineural hearing loss septooptic dysplasia spontaneous ocular nystagmus type 2 diabetes mellitus visual epilepsy
9388	lipase G, endothelial type	LIPG Aliases: EDL	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 Duchenne muscular dystrophy Pick's disease Reye syndrome abdominal obesity-metabolic syndrome 1 acute chest syndrome acute myocardial infarction allergic asthma aortic atherosclerosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis autistic disorder breast cancer breast carcinoma cancer cardiovascular system disease cerebral degeneration cerebral infarction cholesterol-ester transfer protein deficiency coronary artery disease coronary thrombosis dementia depressive disorder diabetes mellitus diabetic cataract diabetic retinopathy embryoma embryonal cancer endometriosis of uterus endometriosis essential hypertension familial hypercholesterolemia familial retinoblastoma germ cell and embryonal cancer germ cell cancer germinoma gestational diabetes heart disease hemolytic-uremic syndrome hyperalphalipoproteinemia 1 hypertension intrinsic asthma muscular dystrophy myocardial infarction nutmeg liver obesity ocular cancer placental insufficiency retinoblastoma sickle cell anemia silent myocardial infarction trilateral retinoblastoma type 2 diabetes mellitus uveal melanoma vascular disease
9382	component of oligomeric golgi complex 1	COG1 Aliases: KIAA1381	Homo sapiens (human)	Baraitser-Winter syndrome Burkitt lymphoma Fraser syndrome Goldenhar syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Richter's syndrome Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome anemia branchiootic syndrome cerebral degeneration cerebrocostomandibular syndrome chronic lymphocytic leukemia clubfoot congenital disorder of glycosylation Ii congenital disorder of glycosylation type I congenital disorder of glycosylation type II congenital disorder of glycosylation type IIg cryptorchidism hematologic cancer hydronephrosis hypospadias kidney failure macrocytic anemia orofaciodigital syndrome I orofaciodigital syndrome X placental insufficiency primary pulmonary hypertension scoliosis sensorineural hearing loss thrombocytopenia
9380	glyoxylate and hydroxypyruvate reductase	GRHPR Aliases: PH2 primary hyperoxaluria type 2	Homo sapiens (human)	atypical hemolytic-uremic syndrome calcinosis calcium metabolism disease chronic kidney disease hemolytic-uremic syndrome hypercalcemia kidney failure nephrocalcinosis nephrolithiasis phosphorus metabolism disease primary hyperoxaluria type 2 primary hyperoxaluria prostate cancer prostate carcinoma ureteral obstruction uric acid nephrolithiasis urinary tract obstruction
9374	palmitoyl-protein thioesterase 2	PPT2	Homo sapiens (human)	cancer cerebellar ataxia cerebellar disease embryoma histiocytosis membranous glomerulonephritis multiple myeloma multiple sclerosis neuroblastoma neuronal ceroid lipofuscinosis 10 neuronal ceroid lipofuscinosis 11 neuronal ceroid lipofuscinosis 13 neuronal ceroid lipofuscinosis 1 neuronal ceroid lipofuscinosis 2 neuronal ceroid lipofuscinosis 3 neuronal ceroid lipofuscinosis 4 neuronal ceroid lipofuscinosis 5 neuronal ceroid lipofuscinosis 6A neuronal ceroid lipofuscinosis 6B neuronal ceroid lipofuscinosis 7 neuronal ceroid lipofuscinosis 8 northern epilepsy variant neuronal ceroid lipofuscinosis 8 neuronal ceroid lipofuscinosis 9 neuronal ceroid lipofuscinosis
9370	adiponectin, C1Q and collagen domain containing	ADIPOQ	Homo sapiens (human)	Alzheimer's disease Behcet's disease Crohn's disease Graves' disease Kawasaki disease Mycobacterium avium complex disease Rett syndrome amyloidosis ankylosing spondylitis atherosclerosis autoimmune hepatitis biliary atresia bipolar disorder brain infarction breast cancer cardiomyopathy cardiovascular system disease chronic obstructive pulmonary disease colitis congestive heart failure coronary aneurysm coronary artery disease dementia diabetic retinopathy diffuse scleroderma end stage renal disease familial hyperlipidemia familial mediterranean fever gestational diabetes graft-versus-host disease hepatocellular carcinoma hyperinsulinism hyperthyroidism inflammatory bowel disease liver cirrhosis metabolic dysfunction-associated steatotic liver disease multiple sclerosis myocardial infarction obesity peripheral artery disease polycystic ovary syndrome primary open angle glaucoma proliferative diabetic retinopathy prostate adenocarcinoma pulmonary tuberculosis rheumatoid arthritis sleep apnea steatotic liver disease tongue squamous cell carcinoma type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis vascular disease
9365	klotho	KL Aliases: KLA alpha-klotho	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 Burkitt lymphoma Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Duchenne muscular dystrophy Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease IgA glomerulonephritis Kummell's disease 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 Pick's disease Prader-Willi syndrome Prinzmetal angina Reye syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Smith-McCort dysplasia Werner syndrome X-linked Aarskog syndrome X-linked dominant hypophosphatemic rickets Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acromegaly actinic keratosis acute myocardial infarction acute pancreatitis adenocarcinoma adenoma adult respiratory distress syndrome alcohol dependence alcohol use disorder alternating hemiplegia of childhood amnestic disorder amyotrophic lateral sclerosis androgen insensitivity syndrome anemia aortic valve disease 1 aortic valve disease aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atrial fibrillation autonomic neuropathy 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 bacterial sepsis beta thalassemia bicuspid aortic valve disease bipolar disorder bladder carcinoma bone disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma calcinosis calcium metabolism disease cancer cardiomyopathy cardiovascular system disease carotid artery disease carotid artery thrombosis carotid stenosis cartilage disease central nervous system disease cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma chondrocalcinosis chondrodysplasia-pseudohermaphroditism syndrome chromophobe renal cell carcinoma chronic fatigue syndrome chronic kidney disease chronic obstructive pulmonary disease clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cone-rod dystrophy congestive heart failure connective tissue disease coronary artery disease coronary stenosis coronary thrombosis cribriform carcinoma dedifferentiated liposarcoma dementia demyelinating disease depressive disorder diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dysthymic disorder embryoma encephalitis encephalomyelitis end stage renal disease endomyocardial fibrosis enthesopathy epilepsy essential hypertension exostosis familial adenomatous polyposis familial hyperlipidemia familial nephrotic syndrome follicular adenoma fundus albipunctatus gastroenteritis giant cell glioblastoma glioblastoma glomerulonephritis granular cell carcinoma growth hormone secreting pituitary adenoma head and neck squamous cell carcinoma heart disease hematologic cancer hepatocellular carcinoma high grade glioma hypercalcemia hyperglycemia hyperinsulinism hyperparathyroidism hyperphosphatemia hyperphosphatemic familial tumoral calcinosis hyperpituitarism hypertension hypertrophic cardiomyopathy hypoglycemia hypophosphatemia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis infertility insulinoma intellectual disability intracranial embolism invasive ductal carcinoma kidney cancer kidney disease kidney failure kidney hypertrophy kwashiorkor large intestine cancer late onset Parkinson's disease learning disability lipoid nephrosis liposarcoma liver cancer liver cirrhosis localized scleroderma lung benign neoplasm lung cancer lung carcinoma lung large cell carcinoma lung non-small cell carcinoma lung small cell carcinoma lung squamous cell carcinoma macrocytic anemia major depressive disorder marasmus melancholic depression melanoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcystic adenoma microphthalmia middle cerebral artery infarction monoclonal gammopathy of uncertain significance mood disorder multiple myeloma multiple sclerosis muscular dystrophy musculoskeletal system disease myelitis myocardial infarction myositis nephritis nephrocalcinosis nephrolithiasis nephrosis nephrotic syndrome nervous system disease neurodegenerative disease neurotic disorder newborn respiratory distress syndrome nonpapillary renal cell carcinoma nutmeg liver nutrition disease obesity obsolete Matthew-Wood syndrome obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma obstructive sleep apnea osteitis fibrosa osteoarthritis osteomalacia osteonecrosis osteoporosis ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatitis papillary adenoma papillary renal cell carcinoma parathyroid adenoma parathyroid carcinoma parathyroid gland disease periarthritis phosphorus metabolism disease placental insufficiency pleomorphic liposarcoma polycystic kidney disease 1 porphyria cutanea tarda postinflammatory pulmonary fibrosis premature menopause priapism primary hyperparathyroidism primary ovarian insufficiency primary pulmonary hypertension progeria progressive muscular atrophy prostate cancer prostate carcinoma protein-energy malnutrition pulmonary emphysema pulmonary fibrosis pulmonary large cell neuroendocrine carcinoma pyoureter reflex sympathetic dystrophy relapsing-remitting multiple sclerosis renal carcinoma renal cell carcinoma renal osteodystrophy retinal disease retinitis pigmentosa 1 retinitis pigmentosa retinitis retrograde amnesia rheumatoid arthritis rickets sarcomatoid renal cell carcinoma schizophrenia scleroderma seborrheic keratosis secondary hyperparathyroidism sickle cell anemia silent myocardial infarction skin disease skin melanoma spondyloarthropathy spondylosis squamous cell carcinoma systemic scleroderma tendinitis thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma tongue squamous cell carcinoma 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 uremia ureteral obstruction uric acid nephrolithiasis urinary bladder cancer vascular dementia vascular disease
9348	N-deacetylase and N-sulfotransferase 3	NDST3 Aliases: HSST3	Homo sapiens (human)	Balo concentric sclerosis adrenoleukodystrophy anxiety disorder autism spectrum disorder azoospermia central nervous system disease depressive disorder generalized anxiety disorder intellectual disability major depressive disorder melancholic depression narcolepsy neurotic disorder obsolete melancholia schizophrenia
9334	beta-1,4-galactosyltransferase 5	B4GALT5 Aliases: beta4-GalT IV beta4GalT-V	Homo sapiens (human)	cancer central nervous system cancer colorectal cancer colorectal carcinoma diabetes mellitus diabetic ketoacidosis embryoma gliosarcoma high grade glioma large intestine cancer mixed glioma multiple sclerosis obesity type 2 diabetes mellitus

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