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 **101 - 125** of **1582** in total

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Gene ID	Gene Name	Gene Symbol ▼	Organism	Disease Ontology
6996	thymine DNA glycosylase	TDG Aliases: G/T mismatch-specific thymine DNA glycosylase	Homo sapiens (human)	adult medulloblastoma benign ependymoma breast cancer breast carcinoma cancer cellular ependymoma childhood medulloblastoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer embryoma embryonal cancer germ cell and embryonal cancer germ cell cancer hepatitis B high grade glioma large intestine cancer medulloblastoma medullomyoblastoma melanotic medulloblastoma multiple myeloma myxopapillary ependymoma pancreatic cancer pancreatic carcinoma papillary ependymoma rectal benign neoplasm rectum adenocarcinoma rectum cancer skin benign neoplasm skin cancer stomach cancer stomach carcinoma tanycytic ependymoma
6916	thromboxane A synthase 1	TBXAS1 Aliases: CYP5 CYP5A1 THAS TS TXAS TXS cytochrome P450, family 5, subfamily A, polypeptide 1	Homo sapiens (human)	Camurati-Engelmann disease Ghosal hematodiaphyseal syndrome acute myocardial infarction acute necrotizing pancreatitis alcoholic hepatitis alcoholic liver cirrhosis allergic asthma anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma ataxia telangiectasia atherosclerosis autosomal recessive osteopetrosis 7 benign mesothelioma brain infarction brain stem infarction breast cancer breast carcinoma cardiovascular system disease cerebral artery occlusion cerebral infarction cerebrovascular disease coronary artery disease coronary thrombosis essential hypertension glomerulonephritis heart disease hydronephrosis hypertension inflammatory bowel disease 1 inflammatory bowel disease intrinsic asthma kidney disease liver cirrhosis lung benign neoplasm macrocytic anemia malignant mesothelioma malignant pleural mesothelioma membranous glomerulonephritis myelofibrosis myocardial infarction nephritis osteopetrosis osteosclerosis pancytopenia pituitary adenoma pituitary cancer pituitary carcinoma platelet-type bleeding disorder 14 prostate cancer prostate carcinoma pulmonary embolism schizophrenia silent myocardial infarction speech disorder thrombocytopenia thrombosis ulcerative colitis urinary bladder cancer
6888	transaldolase 1	TALDO1	Homo sapiens (human)	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease T-cell acute lymphoblastic leukemia acatalasia allergic asthma anemia asthma 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 autoimmune disease autoimmune lymphoproliferative syndrome breast cancer breast carcinoma cancer capillary disease carbohydrate metabolic disorder childhood T-cell acute lymphoblastic leukemia childhood leukemia chronic kidney disease diabetes mellitus diabetic ketoacidosis disease of metabolism gallbladder disease head and neck squamous cell carcinoma hemangioma of liver hepatocellular carcinoma hereditary hemorrhagic telangiectasia immune system disease intrinsic asthma leukemia liver cancer liver cirrhosis liver disease macrocytic anemia multiple sclerosis obsolete T-cell lymphoblastic leukemia/lymphoma oligohydramnios osteomalacia pancytopenia patent ductus arteriosus patent foramen ovale placental insufficiency rickets sensorineural hearing loss sickle cell anemia skin benign neoplasm skin cancer squamous cell carcinoma telangiectasis thrombocytopenia tongue squamous cell carcinoma type 2 diabetes mellitus ventricular septal defect viral infectious disease xeroderma pigmentosum group A xeroderma pigmentosum group B xeroderma pigmentosum group C xeroderma pigmentosum group D xeroderma pigmentosum group E xeroderma pigmentosum group F xeroderma pigmentosum group G xeroderma pigmentosum variant type xeroderma pigmentosum
8871	synaptojanin 2	SYNJ2 Aliases: INPP5H inositol polyphosphate-5-phosphatase H phosphoinositide 5-phosphatase synaptic inositol 1,4,5-trisphosphate 5-phosphatase 2	Homo sapiens (human)	Down syndrome Duchenne muscular dystrophy Joubert syndrome 1 Joubert syndrome Parkinson's disease amyotrophic lateral sclerosis 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 breast cancer bronchus cancer bronchus carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital muscular dystrophy depressive disorder distal myopathy early-onset Parkinson's disease facioscapulohumeral muscular dystrophy giant cell glioblastoma glioblastoma large intestine cancer limb-girdle muscular dystrophy lung cancer lung carcinoma muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 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 progressive muscular atrophy rippling muscle disease 2
8867	synaptojanin 1	SYNJ1 Aliases: INPP5G PARK20 inositol polyphosphate-5-phosphatase G phosphoinositide 5-phosphatase synaptic inositol 1,4,5-trisphosphate 5-phosphatase 1	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Creutzfeldt-Jakob disease Down syndrome Duchenne muscular dystrophy Joubert syndrome 1 Joubert syndrome Laron syndrome Parkinson's disease 19A Parkinson's disease 1 Parkinson's disease 20 Parkinson's disease 23 Parkinson's disease 2 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Unverricht-Lundborg syndrome achondroplasia amnestic disorder amyotrophic lateral sclerosis anodontia attention deficit hyperactivity disorder autistic disorder autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy bipolar disorder blepharospasm blindness borderline personality disorder brain disease cerebral degeneration cone-rod dystrophy congenital muscular dystrophy congenital nystagmus congenital ptosis dementia developmental and epileptic encephalopathy 1 developmental and epileptic encephalopathy 53 dissociated nystagmus distal myopathy dystonia early infantile epileptic encephalopathy early myoclonic encephalopathy early-onset Parkinson's disease epilepsy esophagitis facioscapulohumeral muscular dystrophy focal hand dystonia fundus albipunctatus gastroesophageal reflux disease giant cell glioblastoma glioblastoma high grade glioma intellectual disability intermittent explosive disorder isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia locked-in syndrome microcephaly muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 neuroblastoma neurodegenerative disease obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete infantile epileptic encephalopathy oculopharyngeal muscular dystrophy optic atrophy pathologic nystagmus peptic esophagitis progressive muscular atrophy ptosis quadriplegia retinal degeneration retinitis pigmentosa retrograde amnesia rhabdomyosarcoma rippling muscle disease 2 scoliosis secondary Parkinson disease spontaneous ocular nystagmus status epilepticus tauopathy tooth agenesis visual epilepsy
285362	sulfatase modifying factor 1	SUMF1 Aliases: FGE UNQ3037	Homo sapiens (human)	Balo concentric sclerosis Laron syndrome X-linked chondrodysplasia punctata 1 X-linked ichthyosis achondroplasia adrenoleukodystrophy autosomal dominant cerebellar ataxia autosomal dominant chondrodysplasia punctata autosomal recessive spinocerebellar ataxia 16 blindness breast cancer breast carcinoma cancer cataract central nervous system disease cerebral degeneration chondrodysplasia punctata chronic obstructive pulmonary disease communicating hydrocephalus cystic fibrosis embryoma epilepsy hydrocephalus ichthyosis inherited metabolic disorder intellectual disability learning disability lysosomal storage disease metachromatic leukodystrophy microcephaly mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis mucosulfatidosis multiple sclerosis narcolepsy obstructive hydrocephalus optic atrophy recurrent corneal erosion retinal degeneration rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 schizophrenia senile degeneration of brain sensorineural hearing loss visual epilepsy
6820	sulfotransferase family 2B member 1	SULT2B1 Aliases: HSST2	Homo sapiens (human)	Laron syndrome Sjogren-Larsson syndrome achondroplasia acquired hyperkeratosis autosomal recessive congenital ichthyosis 10 autosomal recessive congenital ichthyosis 14 autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis 2 autosomal recessive congenital ichthyosis 3 autosomal recessive congenital ichthyosis 4A autosomal recessive congenital ichthyosis 5 autosomal recessive congenital ichthyosis 6 autosomal recessive congenital ichthyosis 7 autosomal recessive congenital ichthyosis 8 autosomal recessive congenital ichthyosis 9 autosomal recessive congenital ichthyosis bacterial sepsis cholestasis ectropion endometrial cancer endometrial carcinoma gallbladder cancer gallbladder carcinoma granuloma annulare hepatocellular carcinoma hypotrichosis ichthyosis keratosis follicularis kidney failure liver cancer mongolian spot obsolete congenital ichthyosiform erythroderma otitis media prostate cancer prostate carcinoma pseudoxanthoma elasticum uterine corpus cancer
6783	sulfotransferase family 1E member 1	SULT1E1 Aliases: EST	Homo sapiens (human)	Alzheimer's disease Axenfeld-Rieger syndrome type 2 Creutzfeldt-Jakob disease DiGeorge syndrome Down syndrome Laron syndrome Marfan syndrome Richter's syndrome abdominal obesity-metabolic syndrome 1 achondroplasia acute myocardial infarction acute myocarditis adult lymphoma adult medulloblastoma adult oligodendroglioma alcoholic hepatitis amyotrophic lateral sclerosis androgen insensitivity syndrome ankylosing spondylitis aortic disease arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation autosomal recessive limb-girdle muscular dystrophy type 2C bacterial sepsis bone osteosarcoma brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cannabis abuse cannabis dependence carcinoma cardiomyopathy cardiovascular system disease central nervous system lymphoma cerebral infarction cerebrovascular disease childhood T-cell acute lymphoblastic leukemia childhood lymphoma childhood medulloblastoma childhood oligodendroglioma childhood osteosarcoma cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chronic fatigue syndrome chronic lymphocytic leukemia colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary aneurysm coronary artery disease coronary stenosis coronary thrombosis craniosynostosis cystic fibrosis depressive disorder diabetes mellitus diabetic ketoacidosis diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dysentery dysthymic disorder embryoma encephalomyelitis endometrial cancer endometrial carcinoma endometrial hyperplasia endometriosis of uterus endometriosis endomyocardial fibrosis essential hypertension eye disease familial hypertrophic cardiomyopathy gallbladder disease gastric adenocarcinoma glomerulonephritis head and neck cancer head and neck squamous cell carcinoma heart disease hemochromatosis type 1 hemochromatosis hepatocellular carcinoma hereditary multiple exostoses hidradenitis suppurativa hidradenitis high grade glioma hyperglycemia hypertension hypertrophic cardiomyopathy inferior myocardial infarction inflammatory bowel disease 1 inflammatory bowel disease intellectual disability intermediate coronary syndrome kidney disease large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer learning disability liver cancer liver disease lung benign neoplasm lung cancer lung carcinoma lymphoma major depressive disorder medulloblastoma medullomyoblastoma melancholic depression melanotic medulloblastoma mitochondrial metabolism disease mitral valve stenosis mixed oligodendroglioma-astrocytoma multiple endocrine neoplasia type 1 myocardial infarction nephritis nephrosis neurotic disorder nodular prostate obesity obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma oligodendroglioma osteosarcoma ovarian cancer ovarian carcinoma peripheral artery disease polycystic ovary syndrome pompholyx primary hyperoxaluria primary open angle glaucoma primary pulmonary hypertension progressive muscular atrophy proliferative type fibrocystic change of breast prostate cancer prostate carcinoma prostatic adenoma pyoureter retinal disease retinitis schizophrenia 1 schizophrenia scleroderma severe acute respiratory syndrome silent myocardial infarction situs inversus steatotic liver disease stomach cancer stomach carcinoma systemic scleroderma tetralogy of Fallot thymic carcinoma thymoma transient cerebral ischemia 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 ulcerative colitis uterine corpus cancer velocardiofacial syndrome vertebrobasilar insufficiency
55959	sulfatase 2	SULF2 Aliases: HSULF-2 KIAA1247 SULF-2	Homo sapiens (human)	acute pancreatitis adenocarcinoma adenoma arthritis arthropathy brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma cribriform carcinoma diabetes mellitus dilated cardiomyopathy 1A dilated cardiomyopathy embryoma endometriosis of ovary endometriosis of uterus endometriosis essential hypertension giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hepatocellular carcinoma high grade glioma hyperlipoproteinemia type III hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis invasive ductal carcinoma large intestine cancer liver cancer liver carcinoma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma mixed glioma neuroblastoma nonpapillary renal cell carcinoma obesity osteoarthritis pancreatic cancer pancreatic carcinoma pancreatitis papillary renal cell carcinoma parapsoriasis postinflammatory pulmonary fibrosis prostate cancer prostate carcinoma psoriasis pulmonary fibrosis pure red-cell aplasia pustulosis of palm and sole renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma seminoma skin benign neoplasm skin cancer squamous cell carcinoma stomach cancer stomach carcinoma testicular cancer testis seminoma tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus uveal melanoma
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
8801	succinate-CoA ligase GDP-forming subunit beta	SUCLG2	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Pick's disease Reye syndrome cerebral degeneration endometriosis of ovary endometriosis methylmalonic acidemia prostate cancer prostate carcinoma
8802	succinate-CoA ligase GDP/ADP-forming subunit alpha	SUCLG1	Homo sapiens (human)	Leigh disease McCune Albright syndrome brain disease cardiomyopathy central nervous system cancer cerebral degeneration endomyocardial fibrosis epilepsy familial hypertrophic cardiomyopathy giant cell glioblastoma glioblastoma gliosarcoma high grade glioma hypertrophic cardiomyopathy hypoglycemia hypophosphatemia intellectual disability lactic acidosis learning disability methylmalonic acidemia mitochondrial DNA depletion syndrome 5 mitochondrial DNA depletion syndrome 9 mitochondrial DNA depletion syndrome mitochondrial encephalomyopathy mixed glioma skin disease stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 visual epilepsy
8803	succinate-CoA ligase ADP-forming subunit beta	SUCLA2 Aliases: succinate--CoA ligase (ADP-forming)	Homo sapiens (human)	3-methylglutaconic aciduria type 4 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 Creutzfeldt-Jakob disease Crohn's colitis Crohn's disease Down syndrome Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Laron syndrome Leigh disease Lewy body dementia Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome achondroplasia age related macular degeneration alternating hemiplegia of childhood amnestic disorder amyloidosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autonomic neuropathy blindness central nervous system disease cerebral degeneration congenital ptosis congestive heart failure coronary artery disease cutaneous porphyria degeneration of macula and posterior pole dementia depressive disorder diabetes mellitus diabetic ketoacidosis dissociative amnesia dysthymic disorder dystonia enterocele epilepsy erythropoietic protoporphyria familial retinoblastoma focal hand dystonia frontotemporal dementia generalized dystonia herpes simplex hydrocephalus hypertropia inflammatory bowel disease 1 inflammatory bowel disease isolated elevated serum creatine phosphokinase levels lactic acidosis leukopenia lingual-facial-buccal dyskinesia macular degeneration major depressive disorder mechanical strabismus melancholic depression methylmalonic acidemia microcephaly mitochondrial DNA depletion syndrome 5 mitochondrial DNA depletion syndrome 9 mitochondrial DNA depletion syndrome mitochondrial encephalomyopathy movement disease nervous system disease neuroblastoma neurodegenerative disease neuropathy neurotic disorder obesity obsolete melancholia ophthalmoplegia parasitic helminthiasis infectious disease peripheral nervous system disease ptosis retinoblastoma retrocochlear disease retrograde amnesia sensorineural hearing loss sideroblastic anemia 1 strabismus trichohepatoenteric syndrome 1 trichohepatoenteric syndrome trilateral retinoblastoma tuberculosis type 2 diabetes mellitus ulcerative colitis vascular dementia visual epilepsy
201595	STT3 oligosaccharyltransferase complex catalytic subunit B	STT3B Aliases: Dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3B FLJ90106 SIMP STT3-B dolichyl-diphosphooligosaccharide protein glycotransferase source of immunodominant MHC associated peptides	Homo sapiens (human)	Japanese encephalitis congenital disorder of glycosylation Iw congenital disorder of glycosylation Ix congenital disorder of glycosylation cryptorchidism dengue disease epilepsy intellectual disability learning disability microcephaly optic atrophy placental insufficiency sleeping sickness thrombocytopenia trypanosomiasis viral infectious disease visual epilepsy yellow fever
3703	STT3 oligosaccharyltransferase complex catalytic subunit A	STT3A Aliases: MGC9042 STT3-A TMC dolichyl-diphosphooligosaccharide protein glycotransferase	Homo sapiens (human)	IgA glomerulonephritis anthrax disease attention deficit hyperactivity disorder bipolar disorder cervical adenocarcinoma cervical cancer cervix carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital disorder of glycosylation Iw congenital disorder of glycosylation type I congenital disorder of glycosylation depressive disorder epidermodysplasia verruciformis focal epilepsy herpes simplex large intestine cancer major depressive disorder melancholic depression microcephaly mucoepidermoid carcinoma obsolete melancholia partial motor epilepsy schizophrenia skin benign neoplasm skin cancer skin squamous cell carcinoma sleeping sickness thyroid gland follicular carcinoma trypanosomiasis visual epilepsy
412	steroid sulfatase	STS Aliases: ARSC arylsulfatase C steryl-sulfatase	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 Barrett's esophagus Chagas disease Cockayne syndrome Cornelia de Lange syndrome Creutzfeldt-Jakob disease Down syndrome Dubowitz syndrome Evans' syndrome 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 Joubert syndrome Kallmann syndrome Kawasaki disease Klinefelter syndrome Laron syndrome Miller-Dieker lissencephaly syndrome Mycobacterium avium complex 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 Patau syndrome Pick's disease Prader-Willi syndrome Renpenning syndrome Reye syndrome Robinow syndrome Seckel syndrome Sertoli cell-only syndrome Sheehan syndrome Silver-Russell syndrome Sjogren's syndrome Sjogren-Larsson syndrome Smith-Lemli-Opitz syndrome Smith-Magenis syndrome Streptococcus pneumonia T-cell acute lymphoblastic leukemia Usher syndrome type 1 X-linked Aarskog syndrome X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 X-linked ichthyosis Y-linked spermatogenic failure 1 abdominal obesity-metabolic syndrome 1 achondroplasia achromatopsia acoustic neuroma acquired color blindness acquired hyperkeratosis acquired immunodeficiency syndrome actinic keratosis acute biphenotypic leukemia acute leukemia acute myeloid leukemia adenocarcinoma in situ adenocarcinoma adenoma adult fibrosarcoma adult liposarcoma adult lymphoma alcoholic hepatitis allergic asthma alopecia amnestic disorder amyloidosis anaplastic astrocytoma androgen insensitivity syndrome androgenic alopecia angioimmunoblastic T-cell lymphoma angiomatous meningioma anhidrosis anogenital venereal wart antithrombin III deficiency aortic valve disease 1 aortic valve disease 2 aortic valve disease aortic valve insufficiency aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy ascending cholangitis asthma ataxia with oculomotor apraxia type 1 atherosclerosis atrial fibrillation attention deficit hyperactivity disorder autism spectrum disorder autistic disorder autoimmune thrombocytopenic purpura autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant chondrodysplasia punctata autosomal recessive Robinow syndrome autosomal recessive congenital ichthyosis 10 autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis 2 autosomal recessive congenital ichthyosis 3 autosomal recessive congenital ichthyosis 4A autosomal recessive congenital ichthyosis 5 autosomal recessive congenital ichthyosis 6 autosomal recessive congenital ichthyosis 7 autosomal recessive congenital ichthyosis 8 autosomal recessive congenital ichthyosis 9 autosomal recessive congenital ichthyosis azoospermia bacterial infectious disease bacterial sepsis benign meningioma bicuspid aortic valve disease bile duct adenocarcinoma bile duct carcinoma bladder carcinoma blastomycosis blue color blindness bone osteosarcoma brain cancer brain infarction breast cancer breast carcinoma breast fibroadenoma bronchus cancer bronchus carcinoma calcinosis calcium metabolism disease cancer carcinoma cataract 9 multiple types cellular schwannoma central nervous system lymphoma cerebral cavernous malformation 1 cerebral convexity meningioma cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood cerebral astrocytoma childhood liposarcoma childhood lymphoma childhood osteosarcoma cholangiocarcinoma cholangitis cholera cholesteatoma chondrodysplasia punctata chondrodysplasia-pseudohermaphroditism syndrome chorioamnionitis chromophobe renal cell carcinoma chronic fatigue syndrome chronic kidney disease chronic obstructive pulmonary disease clear cell meningioma clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colonic benign neoplasm color blindness colorectal cancer colorectal carcinoma common wart communication disorder complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital nystagmus congestive heart failure corneal dystrophy coronary artery disease cribriform carcinoma cryptorchidism cutaneous fibrous histiocytoma cystic fibrosis dedifferentiated liposarcoma dermatitis diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma disease of metabolism dissociated nystagmus distal arthrogryposis embryoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma endometrial hyperplasia endometriosis of uterus endometriosis epidermodysplasia verruciformis epidermolysis bullosa dystrophica epidermolytic hyperkeratosis epilepsy epithelioid sarcoma esophagus adenocarcinoma essential hypertension essential thrombocythemia essential tremor eunuchism familial mediterranean fever familial nephrotic syndrome fibrillary astrocytoma fibrosarcoma fibrous meningioma gallbladder disease gastroenteritis gastrointestinal system disease gastroparesis gastroschisis gemistocytic astrocytoma generalized anxiety disorder giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis granular cell carcinoma hemochromatosis type 1 hemochromatosis hepatic coma hepatic encephalopathy hepatitis C hepatocellular carcinoma hidradenoma high grade glioma human immunodeficiency virus infectious disease hydranencephaly hyperandrogenism hypercalcemia hypertension hypogonadism hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypohidrosis hypoparathyroidism-deafness-renal disease syndrome hypoparathyroidism hypopituitarism ichthyosis vulgaris ichthyosis ileitis ileocolitis in situ carcinoma inflammatory bowel disease inherited metabolic disorder intellectual disability intestinal disease intrahepatic cholangiocarcinoma intraorbital meningioma intraventricular meningioma intrinsic asthma 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 juvenile pilocytic astrocytoma keratoconjunctivitis sicca keratosis follicularis kidney disease kidney failure language disorder large intestine cancer laryngeal squamous cell carcinoma learning disability leprosy lipoid nephrosis liposarcoma lissencephaly liver cancer liver carcinoma liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung oat cell carcinoma lung small cell carcinoma lymphoma malignant astrocytoma malignant peripheral nerve sheath tumor melanoma melanotic neurilemmoma melioidosis meningioma meningothelial meningioma metachromatic leukodystrophy mevalonic aciduria microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcystic meningioma middle cerebral artery infarction migraine mixed glioma mixed oligodendroglioma-astrocytoma mongolian spot mood disorder mucosulfatidosis myelitis myelodysplastic syndrome myelofibrosis nephritis nephrocalcinosis nephronophthisis 1 nephrosis nephrotic syndrome neurilemmoma neurodegenerative disease nodular prostate non-suppurative otitis media non-syndromic X-linked intellectual disability nonpapillary renal cell carcinoma obesity obsolete congenital ichthyosiform erythroderma obsolete ymphosarcoma ocular albinism 1 olfactory groove meningioma oligospermia osteoarthritis osteosarcoma otitis media ovarian cancer ovarian carcinoma palindromic rheumatism pancreatic adenocarcinoma panhypopituitarism papillary renal cell carcinoma papilloma paracoccidioidomycosis parapsoriasis parasagittal meningioma patent ductus arteriosus pathologic nystagmus periodontitis peripheral vascular disease phosphorus metabolism disease pilocytic astrocytoma pituitary adenoma pituitary cancer pituitary carcinoma placental choriocarcinoma pleomorphic adenoma pleomorphic liposarcoma plexiform schwannoma pneumocystosis pneumonia polycystic ovary syndrome polyp of middle ear pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 postpartum depression primary sclerosing cholangitis prostate cancer prostate carcinoma prostatic adenoma protein C deficiency protein S deficiency protoplasmic astrocytoma psammomatous meningioma pseudohypoparathyroidism pseudoxanthoma elasticum psoriasis pustulosis of palm and sole pyoureter recessive dystrophic epidermolysis bullosa recurrent corneal erosion red color blindness red-green color blindness renal carcinoma renal cell carcinoma respiratory syncytial virus infectious disease retinal disease retinitis retrograde amnesia rheumatoid arthritis rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia sclerosing cholangitis seborrheic keratosis secretory meningioma seminoma septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly skin disease skin melanoma skin papilloma skin tag speech disorder spinal meningioma spindle cell sarcoma spontaneous ocular nystagmus squamous cell carcinoma squamous cell papilloma steatotic liver disease stomach cancer stomach carcinoma subependymal giant cell astrocytoma suppurative cholangitis syndromic X-linked intellectual disability Najm type syringoma testicular cancer testicular germ cell cancer testis seminoma thrombophilia tick-borne encephalitis tongue squamous cell carcinoma transitional meningioma trichohepatoenteric syndrome 1 trichohepatoenteric syndrome trypanosomiasis tuberculosis tubular adenocarcinoma type 2 diabetes mellitus urinary bladder cancer uterine corpus cancer varicose veins vasculitis visual epilepsy
83931	serine/threonine kinase 40	STK40	Homo sapiens (human)
8987	starch binding domain 1	STBD1 Aliases: FLJ41801 GENX-3414 genethonin 1	Homo sapiens (human)	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease glycogen storage disease II
338596	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 6	ST8SIA6 Aliases: ST8Sia VI	Homo sapiens (human)	acute lymphoblastic leukemia lymphoblastic lymphoma
29906	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5	ST8SIA5 Aliases: ST8Sia V	Homo sapiens (human)	idiopathic scoliosis
7903	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	ST8SIA4 Aliases: PST PST1 ST8Sia IV	Homo sapiens (human)	Duchenne muscular dystrophy Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Norum disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Tangier disease abetalipoproteinemia acne acute pancreatitis adrenoleukodystrophy alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis alternating hemiplegia of childhood anal carcinoma in situ anaplastic astrocytoma ankylosing spondylitis arteriosclerotic cardiovascular disease atherosclerosis autonomic neuropathy breast cancer breast carcinoma bronchus cancer bronchus carcinoma bulimia nervosa cancer carcinoma carotid artery thrombosis carotid stenosis central nervous system disease cerebral infarction cerebrovascular disease cervix uteri carcinoma in situ childhood cerebral astrocytoma childhood leukemia cholecystolithiasis choledocholithiasis cholelithiasis choreaacanthocytosis chromophobe renal cell carcinoma chronic kidney disease chronic myeloid leukemia clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma complement deficiency coronary artery disease depressive disorder diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy diarrhea dysthymic disorder embryoma esophageal cancer esophageal carcinoma essential hypertension fibrillary astrocytoma fragile X syndrome gallbladder cancer gallbladder carcinoma gallbladder disease gemistocytic astrocytoma giant cell glioblastoma glioblastoma glomerulonephritis gyrate atrophy hepatocellular carcinoma hereditary spherocytosis high grade glioma hypertension hypolipoproteinemia hypoparathyroidism juvenile pilocytic astrocytoma kidney disease large intestine cancer laryngeal squamous cell carcinoma leukemia liver cancer liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma major depressive disorder malignant astrocytoma melancholic depression muscular dystrophy myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 nephritis nervous system disease neuroblastoma neurotic disorder nonpapillary renal cell carcinoma nutmeg liver obsolete melancholia pancreatitis papillary renal cell carcinoma papilloma periodontitis pilocytic astrocytoma pneumonia prostate cancer prostate carcinoma protoplasmic astrocytoma pseudohypoparathyroidism renal carcinoma renal cell carcinoma rhabdomyosarcoma rhinitis sarcoidosis sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia sinusitis squamous cell carcinoma squamous cell papilloma steatotic liver disease subependymal giant cell astrocytoma substance abuse substance-related disorder systemic lupus erythematosus thyroid gland follicular carcinoma tongue squamous cell carcinoma type 2 diabetes mellitus uveoparotid fever
51046	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3	ST8SIA3 Aliases: ST8Sia III	Homo sapiens (human)	acute myeloid leukemia basal ganglia disease cancer embryoma schizophrenia
8128	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	ST8SIA2 Aliases: HsT19690 ST8SIA-II STX	Homo sapiens (human)	adenocarcinoma adenoma allergic rhinitis anaplastic astrocytoma autism spectrum disorder autistic disorder bipolar disorder breast cancer breast carcinoma cancer childhood cerebral astrocytoma colitis cribriform carcinoma diarrhea disease of mental health embryoma epilepsy fibrillary astrocytoma gastroenteritis gemistocytic astrocytoma granular cell carcinoma hemolytic-uremic syndrome high grade glioma ileitis ileocolitis intestinal infectious disease juvenile pilocytic astrocytoma lung cancer lung non-small cell carcinoma malignant astrocytoma mood disorder neuroblastoma pilocytic astrocytoma protoplasmic astrocytoma psychotic disorder rhabdomyosarcoma schizophrenia shigellosis subependymal giant cell astrocytoma tubular adenocarcinoma vasomotor rhinitis
6489	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1	ST8SIA1 Aliases: ST8Sia I	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Pick's disease Reye syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis breast cancer breast carcinoma cancer central nervous system cancer cerebral degeneration chronic myeloid leukemia colorectal cancer colorectal carcinoma coronary artery disease endocrine exophthalmos gallbladder disease giant cell glioblastoma glioblastoma gliosarcoma high grade glioma invasive ductal carcinoma large intestine cancer liver disease lung benign neoplasm lung carcinoma melanoma mixed glioma multiple sclerosis neuroblastoma primary immunodeficiency disease secondary Parkinson disease skin melanoma thromboangiitis obliterans toxic encephalopathy
30815	ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 6	ST6GALNAC6 Aliases: ST6GALNACVI	Homo sapiens (human)	kidney cancer

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