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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 **376 - 400** of **1582** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
83650	solute carrier family 35 member G5	SLC35G5	Homo sapiens (human)
401494	3-hydroxyacyl-CoA dehydratase 4	HACD4 Aliases: Em:AL662879.1 OTTHUMG00000021016 Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 4	Homo sapiens (human)	arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cancer
4125	mannosidase alpha class 2B member 1	MAN2B1 Aliases: LAMAN lysosomal alpha-mannosidase	Homo sapiens (human)	IgA glomerulonephritis Klippel-Feil syndrome age related macular degeneration alpha-mannosidosis aspartylglucosaminuria cerebral degeneration congenital nystagmus degeneration of macula and posterior pole dissociated nystagmus fucosidosis gingival hypertrophy gingival overgrowth glycogen storage disease II hypertrichosis inguinal hernia intellectual disability learning disability lingual-facial-buccal dyskinesia lysosomal storage disease macular degeneration methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency movement disease mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis pathologic nystagmus retinal degeneration sensorineural hearing loss spondylolisthesis spontaneous ocular nystagmus
2203	fructose-bisphosphatase 1	FBP1	Homo sapiens (human)	B-cell lymphoma Marfan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Rett syndrome acute myocardial infarction bile duct adenocarcinoma bile duct carcinoma bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer cervical adenocarcinoma cervical cancer cervix carcinoma childhood osteosarcoma cholangiocarcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary thrombosis cryptococcosis cystinuria diabetes mellitus diabetic ketoacidosis diarrhea diffuse large B-cell lymphoma distal arthrogryposis embryoma epilepsy follicular lymphoma fructose-1,6-bisphosphatase deficiency galactosemia giant cell glioblastoma glioblastoma gliosarcoma glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hemolytic anemia hepatitis C hepatitis hepatocellular carcinoma high grade glioma hydrocephalus hyperuricemia hypoglycemia intellectual disability intrahepatic cholangiocarcinoma lactic acidosis large intestine cancer learning disability liver cancer liver carcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma maturity-onset diabetes of the young microphthalmia mixed glioma myocardial infarction neonatal jaundice nonpapillary renal cell carcinoma obsolete Matthew-Wood syndrome obsolete ymphosarcoma osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary renal cell carcinoma prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia silent myocardial infarction situs inversus squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma tongue squamous cell carcinoma tuberous sclerosis type 2 diabetes mellitus viral infectious disease visual epilepsy
1798	dolichyl-phosphate N-acetylglucosaminephosphotransferase 1	DPAGT1 Aliases: ALG7 CDG-Ij D11S366 DGPT GPT GlcNAc-1-P transferase 1 UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase 1	Homo sapiens (human)	Bell's palsy Ebola hemorrhagic fever Lambert-Eaton myasthenic syndrome acute intermittent porphyria agnosia alternating exotropia breast cancer cancer cataract clubfoot colorectal cancer colorectal carcinoma congenital disorder of glycosylation Ij congenital disorder of glycosylation type I congenital disorder of glycosylation congenital myasthenic syndrome 13 congenital myasthenic syndrome congenital nystagmus congenital ptosis cutaneous leishmaniasis developmental and epileptic encephalopathy 36 developmental coordination disorder dissociated nystagmus epilepsy essential hypertension exotropia facial nerve disease facial paralysis familial periodic paralysis fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome glycoproteinosis hepatocellular carcinoma hypertension intellectual disability isolated elevated serum creatine phosphokinase levels large intestine cancer learning disability leishmaniasis liver cancer microcephaly monocular exotropia mucolipidosis II alpha/beta myopathy pathologic nystagmus pseudosarcomatous fibromatosis ptosis scoliosis spontaneous ocular nystagmus squamous cell carcinoma stomach cancer stomach carcinoma stuttering syndromic X-linked intellectual disability 94 tongue squamous cell carcinoma tuberculosis visceral leishmaniasis visual epilepsy
5502	protein phosphatase 1 regulatory inhibitor subunit 1A	PPP1R1A	Homo sapiens (human)
137797	LY6/PLAUR domain containing 2	LYPD2 Aliases: RGTR430 UNQ430	Homo sapiens (human)
4534	myotubularin 1	MTM1	Homo sapiens (human)	Bell's palsy 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 4 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 IgA glomerulonephritis Poland syndrome X-linked dilated cardiomyopathy abdominal obesity-metabolic syndrome 1 adult respiratory distress syndrome agenesis of the corpus callosum with peripheral neuropathy atrioventricular block autosomal dominant centronuclear myopathy autosomal recessive centronuclear myopathy breast cancer breast carcinoma cancer capillary hemangioma cavernous hemangioma centronuclear myopathy 1 centronuclear myopathy X-linked centronuclear myopathy chronic kidney disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer communicating hydrocephalus congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital myopathy 1A congenital myopathy 4A congenital ptosis congenital structural myopathy cryptorchidism cystinuria dental caries dentin caries diabetes mellitus diabetic ketoacidosis diaphragmatic eventration diarrhea dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy embryoma endocarditis epilepsy facial nerve disease facial paralysis familial periodic paralysis galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease hemangioma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 hydrocephalus infective endocarditis intrahepatic cholestasis large intestine cancer megaconial type congenital muscular dystrophy motor peripheral neuropathy muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 myofibrillar myopathy 1 myopathy myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 nemaline myopathy neurodegenerative disease neuromuscular disease neuropathy newborn respiratory distress syndrome obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obstructive hydrocephalus oculocerebrorenal syndrome ophthalmoplegia peripheral nervous system disease placental insufficiency polyhydramnios polyneuropathy ptosis pyloric stenosis rabies rigid spine muscular dystrophy 1 scoliosis senile degeneration of brain subacute bacterial endocarditis tubular aggregate myopathy 1 type 2 diabetes mellitus visual epilepsy
11313	lysophospholipase 2	LYPLA2 Aliases: APT-2 acyl-protein thioesterase 2	Homo sapiens (human)	familial combined hyperlipidemia melanoma skin melanoma
8527	diacylglycerol kinase delta	DGKD Aliases: DGKdelta KIAA0145 diglyceride kinase	Homo sapiens (human)	Lennox-Gastaut syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease cancer diabetes mellitus embryoma epilepsy hyperglycemia nephrolithiasis obsessive-compulsive disorder open-angle glaucoma primary open angle glaucoma type 2 diabetes mellitus uric acid nephrolithiasis visual epilepsy
6675	UDP-N-acetylglucosamine pyrophosphorylase 1	UAP1 Aliases: AGX1 AgX UDP-N-acetylglucosamine diphosphorylase 1 UDP-N-acetylhexosamine pyrophosphorylase 1	Homo sapiens (human)	hepatitis B hepatocellular carcinoma liver cancer pneumocystosis
256356	glycerol kinase 5	GK5	Homo sapiens (human)
79623	polypeptide N-acetylgalactosaminyltransferase 14	GALNT14 Aliases: FLJ12691 GalNac-T10 GalNac-T14 polypeptide GalNAc transferase 14	Homo sapiens (human)	Balo concentric sclerosis Cockayne syndrome Cornelia de Lange syndrome 1 Cornelia de Lange syndrome Dubowitz 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 acute myeloid leukemia adrenoleukodystrophy autistic disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome basal cell carcinoma breast cancer breast carcinoma cancer central nervous system disease chondrodysplasia-pseudohermaphroditism syndrome colorectal cancer colorectal carcinoma corneal disease embryoma esophagus squamous cell carcinoma giant cell glioblastoma glioblastoma hepatocellular carcinoma high grade glioma keratoconus large intestine cancer liver cancer liver carcinoma lung adenocarcinoma lung cancer lung non-small cell carcinoma melanoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II narcolepsy neuroblastoma otitis media ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma signet ring cell adenocarcinoma skin melanoma
93611	F-box protein 44	FBXO44 Aliases: FBG3 FBX30 Fbx44 Fbxo6a MGC14140	Homo sapiens (human)	polycystic ovary syndrome prostate cancer prostate carcinoma
1718	24-dehydrocholesterol reductase	DHCR24 Aliases: Delta(24)-sterol reductase KIAA0018 seladin-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 Clouston syndrome Creutzfeldt-Jakob disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Joubert syndrome Laron syndrome Marfan syndrome Miller-Dieker lissencephaly syndrome Pick's disease Potter's syndrome Q fever Reye syndrome X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 achondroplasia acoustic neuroma actinic keratosis acute myocardial infarction adenocarcinoma adenoma adrenal adenoma adrenal carcinoma adrenal cortex cancer adrenal gland cancer adrenocortical carcinoma adult cystic teratoma adult respiratory distress syndrome adult teratoma angiomatous meningioma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthropathy atherosclerosis autism spectrum disorder autistic disorder autosomal dominant chondrodysplasia punctata autosomal dominant osteopetrosis 2 autosomal recessive osteopetrosis 7 bacterial sepsis benign meningioma bilateral renal aplasia bladder carcinoma brain cancer breast cancer breast carcinoma breast fibroadenoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer cerebral convexity meningioma cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma chondrodysplasia punctata chromophobe renal cell carcinoma chronic kidney disease chronic obstructive pulmonary disease clear cell meningioma clear cell renal cell carcinoma cleft palate clubfoot collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital nystagmus coronary artery disease coronary thrombosis cortical dysplasia-focal epilepsy syndrome cribriform carcinoma cutaneous mastocytosis cystic teratoma diffuse cutaneous mastocytosis disorder of sexual development dissociated nystagmus embryoma endometrial cancer endometrial carcinoma epilepsy epithelioid leiomyosarcoma epithelioid sarcoma esophageal cancer esophageal carcinoma familial adenomatous polyposis fibrous meningioma follicular adenoma giant cell glioblastoma gingival overgrowth glioblastoma gliosarcoma glucose metabolism disease granular cell carcinoma head and neck squamous cell carcinoma hepatitis C hepatocellular carcinoma hermaphroditism high grade glioma hydranencephaly hydrocephalus hypertropia inflammatory breast carcinoma insulinoma intellectual disability intraorbital meningioma intraventricular meningioma invasive ductal carcinoma islet cell tumor isolated cleft palate kidney cancer large intestine cancer learning disability leiomyoma leiomyosarcoma lipid metabolism disorder lissencephaly liver cancer lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lymphoplasmacyte-rich meningioma malignant teratoma mastocytosis mature teratoma mechanical strabismus melanoma meningioma meningothelial meningioma microcephaly microcystic adenoma microcystic meningioma migraine without aura mixed glioma multiple myeloma multiple sclerosis myocardial infarction myofibroma myxoid leiomyosarcoma nasopharynx carcinoma neuroblastoma neurodegenerative disease neurogenic arthropathy obstructive hydrocephalus olfactory groove meningioma ophthalmoplegia osteomyelitis osteopetrosis osteosclerosis ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma parasagittal meningioma patent ductus arteriosus pathologic nystagmus pituitary adenoma placental insufficiency pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 prostate cancer prostate carcinoma psammomatous meningioma pseudohermaphroditism rectal benign neoplasm rectum adenocarcinoma rectum cancer relapsing-remitting multiple sclerosis renal cell carcinoma rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma scimitar syndrome seborrheic keratosis secretory meningioma senile degeneration of brain septooptic dysplasia serous cystadenocarcinoma short-rib thoracic dysplasia 14 with polydactyly silent myocardial infarction situs inversus skin atrophy skin disease skin melanoma spinal meningioma spindle cell sarcoma spontaneous ocular nystagmus status epilepticus strabismus syndromic X-linked intellectual disability Najm type synovitis tenosynovitis teratoma thyroid gland papillary carcinoma transient cerebral ischemia transitional cell carcinoma transitional meningioma trigeminal neuralgia trypanosomiasis tuberous sclerosis tubular adenocarcinoma typhus ureteric orifice cancer urinary bladder cancer urticaria pigmentosa uterine corpus cancer uterine fibroid vertebrobasilar insufficiency visual epilepsy
4350	N-methylpurine DNA glycosylase	MPG Aliases: MDG alkyladenine DNA glycosylase	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 Bloch-Sulzberger syndrome IgA glomerulonephritis Pick's disease Reye syndrome adenocarcinoma adenoma anal carcinoma in situ anemia aortic valve disease 2 aortic valve stenosis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer cerebral degeneration cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ chikungunya colorectal cancer colorectal carcinoma common wart dengue hemorrhagic fever depressive disorder diabetes mellitus diabetic ketoacidosis dysthymic disorder embryoma eosinophilic esophagitis esophagus adenocarcinoma familial retinoblastoma follicular adenoma gallbladder cancer gallbladder carcinoma giant cell glioblastoma glioblastoma gliosarcoma hepatitis C hepatocellular carcinoma high grade glioma hyperglycemia hypomelanosis of Ito idiopathic interstitial pneumonia idiopathic pulmonary fibrosis inflammatory bowel disease 1 inflammatory bowel disease large intestine cancer leishmaniasis liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma macrocytic anemia major depressive disorder male infertility melancholic depression melanoma microcystic adenoma mixed glioma multiple myeloma neurotic disorder obsolete melancholia papillary adenoma polycystic ovary syndrome postinflammatory pulmonary fibrosis pulmonary fibrosis retinoblastoma rheumatoid arthritis sarcomatoid carcinoma skin melanoma trilateral retinoblastoma tuberculosis type 2 diabetes mellitus ulcerative colitis visceral leishmaniasis xeroderma pigmentosum group C
7365	UDP glucuronosyltransferase family 2 member B10	UGT2B10	Homo sapiens (human)	cancer embryoma prostate cancer prostate carcinoma
253430	inositol polyphosphate multikinase	IPMK	Homo sapiens (human)	Alzheimer's disease Crohn's colitis Crohn's disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease cancer hepatitis idiopathic scoliosis inflammatory bowel disease 1 inflammatory bowel disease ovarian cancer ovarian carcinoma parapsoriasis psoriasis pustulosis of palm and sole ulcerative colitis
2619	growth arrest specific 1	GAS1	Homo sapiens (human)	Baraitser-Winter syndrome Fraser syndrome Goldenhar syndrome Kallmann syndrome Laron syndrome Marfan syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Potter's syndrome Sakati-Nyhan syndrome Sheehan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome achondroplasia allergic asthma asthma bilateral renal aplasia bladder carcinoma bone osteosarcoma branchiootic syndrome breast cancer breast carcinoma cancer cavernous hemangioma central nervous system cancer childhood osteosarcoma choanal atresia chorioangioma chromophobe renal cell carcinoma clear cell renal cell carcinoma cleft palate collecting duct carcinoma coloboma colorectal cancer colorectal carcinoma congenital hypothyroidism degenerative disc disease diabetes mellitus diabetic ketoacidosis disorder of sexual development duodenal atresia embryoma epilepsy gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glomus tumor hemangioma hereditary sensory and autonomic neuropathy type 1 hereditary sensory and autonomic neuropathy type 1A hereditary sensory neuropathy hermaphroditism high grade glioma histiocytoid hemangioma holoprosencephaly 1 holoprosencephaly hypertropia 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 hypothyroidism intellectual disability intramuscular hemangioma 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 kidney disease large intestine cancer learning disability lymphangioma mechanical strabismus melanoma microcephaly mixed glioma myxedema nephritis nephrosis neuroblastoma neuropathy nevoid basal cell carcinoma syndrome nonpapillary renal cell carcinoma ophthalmoplegia orofaciodigital syndrome I orofaciodigital syndrome X osteosarcoma panhypopituitarism papillary adenocarcinoma papillary renal cell carcinoma peripheral nervous system disease placental insufficiency primary open angle glaucoma pseudohermaphroditism pyoureter rabies renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma scoliosis sensorineural hearing loss sensory peripheral neuropathy situs inversus skin melanoma solitary median maxillary central incisor stomach cancer stomach carcinoma strabismus tetralogy of Fallot thymus gland disease thyroid gland papillary carcinoma tuberous sclerosis type 2 diabetes mellitus urinary bladder cancer visual epilepsy
54576	UDP glucuronosyltransferase family 1 member A8	UGT1A8 Aliases: UGT1H	Homo sapiens (human)	Crigler-Najjar syndrome Gaucher's disease Gilbert syndrome abdominal obesity-metabolic syndrome 1 agranulocytosis alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia beta thalassemia bilirubin metabolic disorder bladder carcinoma breast cancer breast carcinoma cancer carcinoma cardiac arrest cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chronic myeloid leukemia colorectal cancer colorectal carcinoma cryptococcosis cystinuria diabetes mellitus diarrhea differentiated thyroid gland carcinoma embryoma epilepsy esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma female reproductive organ cancer galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease Ia glycogen storage disease hemoglobin H disease hepatitis D hereditary spherocytosis influenza kernicterus due to isoimmunization kernicterus large intestine cancer leiomyoma leukopenia liver disease myofibroma neonatal jaundice neutropenia nodular prostate obesity prostate cancer prostate carcinoma prostatic adenoma rheumatoid arthritis sarcomatoid carcinoma schizophrenia severe congenital neutropenia sickle cell anemia steatotic liver disease stomach cancer stomach carcinoma thalassemia type 2 diabetes mellitus urinary bladder cancer uterine fibroid visual epilepsy xeroderma pigmentosum group D
2588	galactosamine (N-acetyl)-6-sulfatase	GALNS Aliases: GALNAC6S GAS GalN6S Morquio syndrome N-acetylgalactosamine-6-sulfatase chondroitinase chondroitinsulfatase galactose-6-sulfate sulfatase mucopolysaccharidosis type IVA	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 GM1 gangliosidosis Laron syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome Wilson disease achondroplasia acne adenine phosphoribosyltransferase deficiency adenocarcinoma adenoma age related macular degeneration amyloidosis anthrax disease anxiety disorder arachnoiditis bacterial meningitis bacterial sepsis bacterial vaginosis bile duct adenocarcinoma bile duct carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiovascular system disease cerebral degeneration cholangiocarcinoma chronic lymphocytic leukemia chronic obstructive pulmonary disease chronic ulcer of skin colorectal cancer colorectal carcinoma cribriform carcinoma degeneration of macula and posterior pole dental caries dentin caries diabetes mellitus diabetic ketoacidosis disease of mental health disease of metabolism embryoma enterocele generalized anxiety disorder glomerulonephritis granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hemochromatosis hole retinal cyst impetigo influenza inguinal hernia intrahepatic cholangiocarcinoma iron metabolism disease kidney disease large intestine cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lysosomal storage disease macular degeneration macular holes mastitis meningitis metachromatic leukodystrophy mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis VI mucopolysaccharidosis type IVB mucopolysaccharidosis multiple epiphyseal dysplasia myositis necrotizing fasciitis nephritis osteochondrodysplasia osteoporosis pharyngitis phobic disorder prostate cancer prostate carcinoma psychotic disorder pyoderma retinal perforation rheumatic fever scarlet fever scoliosis sensorineural hearing loss stomach cancer stomach carcinoma tonsillitis tuberculosis tubular adenocarcinoma type 2 diabetes mellitus vaginitis viral meningitis vulvitis vulvovaginitis
130589	galactose mutarotase	GALM Aliases: aldose 1-epimerase aldose mutarotase galactomutarotase	Homo sapiens (human)	Crohn's colitis Crohn's disease classic galactosemia colitis colorectal cancer colorectal carcinoma galactokinase deficiency galactosemia gastroenteritis ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease 2 inflammatory bowel disease large intestine cancer ulcerative colitis
27159	chitinase acidic	CHIA Aliases: AMCase CHIT2 TSA1902 acidic mammalian chitinase	Homo sapiens (human)	Sjogren's syndrome allergic asthma allergic conjunctivitis allergic rhinitis asthma cryptococcosis dry eye syndrome eosinophilic esophagitis giant papillary conjunctivitis intrinsic asthma keratoconjunctivitis sicca silicosis sinusitis vasomotor rhinitis vernal conjunctivitis xerophthalmia
247	arachidonate 15-lipoxygenase type B	ALOX15B Aliases: 15-LOX-2	Homo sapiens (human)	Clouston syndrome adenocarcinoma adenoma adrenal adenoma adrenal cortex cancer allergic asthma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma colorectal cancer colorectal carcinoma coronary artery disease cribriform carcinoma diabetic ketoacidosis embryoma esophageal cancer esophageal carcinoma essential hypertension granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma hypertension intrinsic asthma large intestine cancer lung cancer lung carcinoma lung non-small cell carcinoma nodular prostate nutmeg liver obsolete type 1 diabetes mellitus 9 parapsoriasis prostate adenocarcinoma prostate cancer prostate carcinoma prostatic adenoma psoriasis pustulosis of palm and sole sarcomatoid 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
9110	myotubularin related protein 4	MTMR4 Aliases: KIAA0647 ZFYVE11	Homo sapiens (human)	Charcot-Marie-Tooth disease anterior horn cell disease benign mesothelioma centronuclear myopathy X-linked herpes simplex malignant mesothelioma muscular atrophy

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