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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 **392376 - 392400** of **393515** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
22933	sirtuin 2	SIRT2	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 Chagas disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Loeffler syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Rett syndrome Reye syndrome Richter's syndrome Werner syndrome abdominal obesity-metabolic syndrome 1 acute myeloid leukemia acute myocardial infarction acute pancreatitis adenocarcinoma adenoma allergic asthma alternating hemiplegia of childhood amyotrophic lateral sclerosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis autonomic neuropathy autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy bacterial infectious disease bacterial sepsis basal cell carcinoma bile duct adenocarcinoma bile duct carcinoma bladder carcinoma brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease central nervous system cancer central nervous system disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cholangiocarcinoma chromophobe renal cell carcinoma chronic apical periodontitis chronic lymphocytic leukemia chronic obstructive pulmonary disease clear cell renal cell carcinoma cocaine dependence collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis cribriform carcinoma cystic fibrosis degenerative disc disease dementia depressive disorder diabetes mellitus diabetic ketoacidosis distal arthrogryposis distal myopathy dysthymic disorder embryoma endometrial cancer endometrial carcinoma eosinophilic pneumonia epithelioid sarcoma essential hypertension facioscapulohumeral muscular dystrophy gastritis gastrointestinal system cancer giant cell glioblastoma glioblastoma gliosarcoma glucose intolerance granular cell carcinoma heart disease hepatitis B hepatitis hepatocellular carcinoma high grade glioma hyperglycemia hypertension inclusion body myositis intermittent claudication intrahepatic cholangiocarcinoma intrinsic asthma large intestine cancer leukemia limb-girdle muscular dystrophy listeriosis liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder melancholic depression melanoma metabolic dysfunction-associated steatotic liver disease middle cerebral artery infarction mixed glioma mood disorder multiple sclerosis muscular dystrophy myocardial infarction nasopharynx carcinoma nervous system disease neurodegenerative disease neurofibromatosis neurotic disorder nonpapillary renal cell carcinoma obesity obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete melancholia obsolete type 1 diabetes mellitus 9 oculopharyngeal muscular dystrophy osteoarthritis osteoporosis ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatitis papillary renal cell carcinoma periapical granuloma periapical periodontitis placental insufficiency prediabetes syndrome primary cutaneous T-cell non-Hodgkin lymphoma progeria progressive muscular atrophy prolymphocytic leukemia prostate cancer prostate carcinoma pulmonary embolism pulmonary eosinophilia renal carcinoma renal cell carcinoma rhabdomyosarcoma sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma secondary Parkinson disease silent myocardial infarction skin benign neoplasm skin cancer skin melanoma spindle cell sarcoma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma synovial sarcoma tongue squamous cell carcinoma trypanosomiasis tuberculosis tubular adenocarcinoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus urethral obstruction urinary bladder cancer uterine corpus cancer vestibular schwannomatosis
22927	hyaluronan binding protein 4	HABP4 Aliases: IHABP4 SERBP1L	Homo sapiens (human)	Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma
22925	phospholipase A2 receptor 1	PLA2R1 Aliases: CLEC13C PLA2-R PLA2G1R PLA2IR	Homo sapiens (human)	IgA glomerulonephritis T-cell acute lymphoblastic leukemia Werner syndrome acute biphenotypic leukemia acute leukemia acute myeloid leukemia adrenoleukodystrophy allergic asthma asthma autoimmune disease autoimmune lymphoproliferative syndrome breast cancer breast carcinoma cancer cardiac arrest childhood leukemia chromophobe renal cell carcinoma chronic kidney disease clear cell renal cell carcinoma collecting duct carcinoma embryoma essential thrombocythemia familial nephrotic syndrome focal segmental glomerulosclerosis glomerulonephritis immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome immune system disease interstitial nephritis intrinsic asthma kidney cancer kidney disease leukemia lipoid nephrosis lupus erythematosus lupus nephritis membranous glomerulonephritis myelodysplastic syndrome nephritis nephrosis nephrotic syndrome nonpapillary renal cell carcinoma papillary renal cell carcinoma progeria prostate cancer prostate carcinoma pyelitis pyelonephritis pyoureter renal carcinoma renal cell carcinoma renal infectious disease sarcomatoid renal cell carcinoma substance abuse substance-related disorder systemic lupus erythematosus thyroid adenoma thyroid cancer thyroid gland carcinoma
22918	CD93 molecule	CD93 Aliases: C1qR(P) C1qRP CDw93 ECSM3 dJ737E23.1	Homo sapiens (human)	Kuhnt-Junius degeneration acute leukemia acute myocardial infarction allergic asthma asthma cancer central nervous system cancer chronic fatigue syndrome coronary artery disease coronary thrombosis embryoma encephalitis encephalomyelitis giant cell glioblastoma glioblastoma gliosarcoma high grade glioma intrinsic asthma lung cancer lung non-small cell carcinoma mixed glioma myelitis myocardial infarction nasopharynx carcinoma parapsoriasis psoriasis pustulosis of palm and sole silent myocardial infarction thyroid gland carcinoma vascular cancer
22914	killer cell lectin like receptor K1	KLRK1 Aliases: CD314 KLR NKG2-D NKG2D	Homo sapiens (human)	B-cell lymphoma Barrett's esophagus Behcet's disease Burkitt lymphoma Crohn's colitis Crohn's disease Ewing sarcoma Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Kaposi's sarcoma Kawasaki disease Langerhans-cell histiocytosis Sezary's disease X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia acute leukemia acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adult lymphoma alopecia alveolar echinococcosis anogenital venereal wart arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asbestosis ataxia telangiectasia atherosclerosis atypical chronic myeloid leukemia, BCR-ABL1 negative autoimmune disease autoimmune hepatitis autoimmune lymphoproliferative syndrome basal cell carcinoma benign deep fibrous histiocytoma benign mesothelioma bile duct adenocarcinoma bile duct carcinoma bone osteosarcoma breast cancer breast carcinoma bronchiolitis obliterans bronchiolitis bronchus cancer bronchus carcinoma byssinosis cancer carcinoma celiac disease central nervous system cancer cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood acute myeloid leukemia childhood leukemia childhood lymphoma childhood osteosarcoma cholangiocarcinoma chronic fatigue syndrome chronic monocytic leukemia chronic obstructive pulmonary disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma cutaneous fibrous histiocytoma diabetes mellitus diabetic ketoacidosis distal arthrogryposis embryoma encephalitis encephalomyelitis endometriosis of uterus endometriosis epithelioid sarcoma esophagus squamous cell carcinoma familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperlipidemia familial retinoblastoma fibrosarcoma gallbladder disease gastrointestinal system cancer giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hepatitis A hepatitis B hepatitis C hepatitis hepatocellular carcinoma high grade glioma histiocytoma hyperglycemia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis immune system disease inflammatory bowel disease 1 inflammatory bowel disease intrahepatic cholangiocarcinoma islet cell tumor large intestine cancer leukemia leukocyte adhesion deficiency 1 leukocyte adhesion deficiency liver cancer liver carcinoma liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus erythematosus lymphoblastic lymphoma lymphoid leukemia lymphoma lymphoproliferative syndrome malignant mesothelioma melanoma mixed glioma monoclonal gammopathy of uncertain significance monocytic leukemia multiple myeloma multiple sclerosis myelitis myeloid leukemia myocardial infarction myocarditis nasopharynx carcinoma neuroblastoma non-Hodgkin lymphoma obsolete ymphosarcoma osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancytopenia paroxysmal nocturnal hemoglobinuria primary sclerosing cholangitis prolactinoma prostate cancer prostate carcinoma refractory plasma cell neoplasm reticulohistiocytic granuloma reticulosarcoma retinoblastoma rheumatoid arthritis sarcoma sclerosing cholangitis sclerosing hemangioma sebaceous carcinoma silent myocardial infarction skin melanoma spindle cell sarcoma spondyloarthropathy spondylosis squamous cell carcinoma squamous cell neoplasm stomach cancer stomach carcinoma sweat gland cancer systemic lupus erythematosus temporal arteritis thyroid gland anaplastic carcinoma tongue squamous cell carcinoma trilateral retinoblastoma tropical spastic paraparesis tuberculosis tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis viral infectious disease
22908	SAC1 like phosphatidylinositide phosphatase	SACM1L Aliases: KIAA0851 SAC1	Homo sapiens (human)	IgA glomerulonephritis T-cell acute lymphoblastic leukemia acute lymphoblastic leukemia adult T-cell leukemia/lymphoma brain infarction breast cancer carotid artery thrombosis carotid stenosis cerebral infarction cerebrovascular disease coronary artery disease diabetes mellitus diabetic ketoacidosis epilepsy essential hypertension glomerulonephritis hemophilia B hypertension kidney disease lymphoblastic lymphoma maturity-onset diabetes of the young nephritis nephrosis obsolete T-cell lymphoblastic leukemia/lymphoma pyoureter rheumatoid arthritis type 2 diabetes mellitus visual epilepsy von Willebrand's disease 3 von Willebrand's disease
22901	arylsulfatase G	ARSG Aliases: KIAA1001	Homo sapiens (human)	Usher syndrome type 2 Usher syndrome type 3 Usher syndrome type 3A Usher syndrome anxiety disorder astigmatism blepharospasm blindness cancer cataract cerebellar ataxia cerebellar disease congenital stationary night blindness 1A congenital stationary night blindness depressive disorder dysthymic disorder dystonia embryoma focal dystonia focal hand dystonia generalized anxiety disorder generalized dystonia lysosomal storage disease major depressive disorder melancholic depression metachromatic leukodystrophy mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis 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 neurotic disorder night blindness obsolete melancholia peripheral retinal degeneration prostate cancer prostate carcinoma retinitis pigmentosa-deafness syndrome schizophrenia scotoma sensorineural hearing loss
22876	inositol polyphosphate-5-phosphatase F	INPP5F Aliases: KIAA0966 Phosphatidylinositide phosphatase SAC2 SAC2 Sac domain-containing inositol phosphatase 2 Sac domain-containing phosphoinositide 4-phosphatase 2 hSac2	Homo sapiens (human)	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease breast cancer diabetes mellitus diabetic ketoacidosis familial hyperlipidemia hyperglycemia type 2 diabetes mellitus
22856	chondroitin sulfate synthase 1	CHSY1 Aliases: CSS1 KIAA0990	Homo sapiens (human)	Laron syndrome X-linked nonsyndromic deafness achondroplasia adult malignant schwannoma anodontia autosomal dominant auditory neuropathy 1 autosomal dominant nonsyndromic deafness 10 autosomal dominant nonsyndromic deafness 11 autosomal dominant nonsyndromic deafness 12 autosomal dominant nonsyndromic deafness 13 autosomal dominant nonsyndromic deafness 15 autosomal dominant nonsyndromic deafness 16 autosomal dominant nonsyndromic deafness 17 autosomal dominant nonsyndromic deafness 18 autosomal dominant nonsyndromic deafness 1 autosomal dominant nonsyndromic deafness 20 autosomal dominant nonsyndromic deafness 21 autosomal dominant nonsyndromic deafness 22 autosomal dominant nonsyndromic deafness 23 autosomal dominant nonsyndromic deafness 24 autosomal dominant nonsyndromic deafness 25 autosomal dominant nonsyndromic deafness 27 autosomal dominant nonsyndromic deafness 28 autosomal dominant nonsyndromic deafness 2A autosomal dominant nonsyndromic deafness 2B autosomal dominant nonsyndromic deafness 30 autosomal dominant nonsyndromic deafness 31 autosomal dominant nonsyndromic deafness 33 autosomal dominant nonsyndromic deafness 36 autosomal dominant nonsyndromic deafness 3A autosomal dominant nonsyndromic deafness 3B autosomal dominant nonsyndromic deafness 40 autosomal dominant nonsyndromic deafness 41 autosomal dominant nonsyndromic deafness 43 autosomal dominant nonsyndromic deafness 44 autosomal dominant nonsyndromic deafness 47 autosomal dominant nonsyndromic deafness 48 autosomal dominant nonsyndromic deafness 49 autosomal dominant nonsyndromic deafness 4A autosomal dominant nonsyndromic deafness 4B autosomal dominant nonsyndromic deafness 50 autosomal dominant nonsyndromic deafness 51 autosomal dominant nonsyndromic deafness 52 autosomal dominant nonsyndromic deafness 53 autosomal dominant nonsyndromic deafness 54 autosomal dominant nonsyndromic deafness 56 autosomal dominant nonsyndromic deafness 58 autosomal dominant nonsyndromic deafness 59 autosomal dominant nonsyndromic deafness 5 autosomal dominant nonsyndromic deafness 64 autosomal dominant nonsyndromic deafness 65 autosomal dominant nonsyndromic deafness 66 autosomal dominant nonsyndromic deafness 67 autosomal dominant nonsyndromic deafness 68 autosomal dominant nonsyndromic deafness 69 autosomal dominant nonsyndromic deafness 6 autosomal dominant nonsyndromic deafness 70 autosomal dominant nonsyndromic deafness 7 autosomal dominant nonsyndromic deafness 9 autosomal dominant nonsyndromic deafness autosomal recessive nonsyndromic deafness 101 autosomal recessive nonsyndromic deafness 102 autosomal recessive nonsyndromic deafness 103 autosomal recessive nonsyndromic deafness 104 autosomal recessive nonsyndromic deafness 12 autosomal recessive nonsyndromic deafness 13 autosomal recessive nonsyndromic deafness 14 autosomal recessive nonsyndromic deafness 15 autosomal recessive nonsyndromic deafness 16 autosomal recessive nonsyndromic deafness 17 autosomal recessive nonsyndromic deafness 18A autosomal recessive nonsyndromic deafness 18B autosomal recessive nonsyndromic deafness 1A autosomal recessive nonsyndromic deafness 1B autosomal recessive nonsyndromic deafness 20 autosomal recessive nonsyndromic deafness 21 autosomal recessive nonsyndromic deafness 22 autosomal recessive nonsyndromic deafness 23 autosomal recessive nonsyndromic deafness 24 autosomal recessive nonsyndromic deafness 25 autosomal recessive nonsyndromic deafness 26 autosomal recessive nonsyndromic deafness 27 autosomal recessive nonsyndromic deafness 28 autosomal recessive nonsyndromic deafness 29 autosomal recessive nonsyndromic deafness 2 autosomal recessive nonsyndromic deafness 30 autosomal recessive nonsyndromic deafness 31 autosomal recessive nonsyndromic deafness 32 autosomal recessive nonsyndromic deafness 33 autosomal recessive nonsyndromic deafness 35 autosomal recessive nonsyndromic deafness 36 autosomal recessive nonsyndromic deafness 37 autosomal recessive nonsyndromic deafness 38 autosomal recessive nonsyndromic deafness 39 autosomal recessive nonsyndromic deafness 3 autosomal recessive nonsyndromic deafness 40 autosomal recessive nonsyndromic deafness 42 autosomal recessive nonsyndromic deafness 44 autosomal recessive nonsyndromic deafness 45 autosomal recessive nonsyndromic deafness 46 autosomal recessive nonsyndromic deafness 47 autosomal recessive nonsyndromic deafness 48 autosomal recessive nonsyndromic deafness 49 autosomal recessive nonsyndromic deafness 4 autosomal recessive nonsyndromic deafness 51 autosomal recessive nonsyndromic deafness 53 autosomal recessive nonsyndromic deafness 55 autosomal recessive nonsyndromic deafness 59 autosomal recessive nonsyndromic deafness 5 autosomal recessive nonsyndromic deafness 61 autosomal recessive nonsyndromic deafness 62 autosomal recessive nonsyndromic deafness 63 autosomal recessive nonsyndromic deafness 65 autosomal recessive nonsyndromic deafness 66 autosomal recessive nonsyndromic deafness 67 autosomal recessive nonsyndromic deafness 68 autosomal recessive nonsyndromic deafness 6 autosomal recessive nonsyndromic deafness 70 autosomal recessive nonsyndromic deafness 71 autosomal recessive nonsyndromic deafness 74 autosomal recessive nonsyndromic deafness 76 autosomal recessive nonsyndromic deafness 77 autosomal recessive nonsyndromic deafness 79 autosomal recessive nonsyndromic deafness 7 autosomal recessive nonsyndromic deafness 83 autosomal recessive nonsyndromic deafness 84A autosomal recessive nonsyndromic deafness 84B autosomal recessive nonsyndromic deafness 85 autosomal recessive nonsyndromic deafness 86 autosomal recessive nonsyndromic deafness 88 autosomal recessive nonsyndromic deafness 89 autosomal recessive nonsyndromic deafness 8 autosomal recessive nonsyndromic deafness 91 autosomal recessive nonsyndromic deafness 93 autosomal recessive nonsyndromic deafness 96 autosomal recessive nonsyndromic deafness 97 autosomal recessive nonsyndromic deafness 98 autosomal recessive nonsyndromic deafness 9 autosomal recessive nonsyndromic deafness breast cancer breast carcinoma cancer childhood malignant schwannoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma embryoma epithelioid malignant peripheral nerve sheath tumor epithelioid sarcoma giant cell glioblastoma glioblastoma hepatocellular carcinoma high grade glioma large intestine cancer liver cancer malignant peripheral nerve sheath tumor myxofibrosarcoma neurilemmoma neurofibrosarcoma neuropathy nonpapillary renal cell carcinoma obsolete autosomal recessive nonsyndromic deafness 105 optic atrophy papillary renal cell carcinoma peripheral nervous system disease renal carcinoma renal cell carcinoma sarcoma sarcomatoid renal cell carcinoma spindle cell sarcoma syndactyly temtamy preaxial brachydactyly syndrome tooth agenesis
22854	netrin G1	NTNG1 Aliases: KIAA0976 Lmnt1 Netrin-G1 netrin G1f	Homo sapiens (human)	Rett syndrome anorexia nervosa autistic disorder bipolar disorder brain disease cancer cerebral infarction cerebrovascular disease cocaine abuse cocaine dependence colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma epilepsy esophagitis gastroesophageal reflux disease head and neck squamous cell carcinoma hydrocephalus intellectual disability large intestine cancer learning disability lingual-facial-buccal dyskinesia microcephaly morphine dependence movement disease nephrolithiasis neuroendocrine carcinoma neuroendocrine tumor neuropathy patent ductus arteriosus peptic esophagitis peripheral nervous system disease polyneuropathy schizophrenia sensorineural hearing loss uric acid nephrolithiasis visual epilepsy
22845	dolichol kinase	DOLK Aliases: DK1 KIAA1094 dolichol kinase 1	Homo sapiens (human)	Marfan syndrome X-linked dilated cardiomyopathy autosomal recessive polycystic kidney disease congenital disorder of glycosylation Im congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 dilated cardiomyopathy 1A dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy ichthyosis isolated elevated serum creatine phosphokinase levels lipoatrophic diabetes mellitus lipodystrophy nonepidermolytic palmoplantar keratoderma palmoplantar keratosis polycystic kidney disease 4 sensorineural hearing loss situs inversus tuberous sclerosis
22796	component of oligomeric golgi complex 2	COG2	Homo sapiens (human)	atrial fibrillation cardiovascular system disease congenital disorder of glycosylation type IIq congenital disorder of glycosylation coronary artery disease diabetes mellitus epilepsy familial hypercholesterolemia heart disease hypobetalipoproteinemia locked-in syndrome obsolete constipation quadriplegia rheumatoid arthritis stomach cancer stomach carcinoma type 2 diabetes mellitus visual epilepsy
22619	sialic acid acetylesterase	Siae	Mus musculus (house mouse)	autoimmune disease
22278	upstream transcription factor 1	Usf1	Mus musculus (house mouse)	cardiovascular system disease type 2 diabetes mellitus
22271	uridine phosphorylase 1	Upp1	Mus musculus (house mouse)	middle cerebral artery infarction
22256	uracil DNA glycosylase	Ung	Mus musculus (house mouse)	dysgammaglobulinemia immunodeficiency with hyper IgM type 5
22247	uridine monophosphate synthetase	Umps	Mus musculus (house mouse)	orotic aciduria purine-pyrimidine metabolic disorder
22239	UDP galactosyltransferase 8A	Ugt8a	Mus musculus (house mouse)
22238	UDP glucuronosyltransferase 2 family, polypeptide B5	Ugt2b5	Mus musculus (house mouse)
22236	UDP glucuronosyltransferase 1 family, polypeptide A2	Ugt1a2	Mus musculus (house mouse)
22234	UDP-glucose ceramide glucosyltransferase	Ugcg	Mus musculus (house mouse)	hypertension
22228	uncoupling protein 2 (mitochondrial, proton carrier)	Ucp2	Mus musculus (house mouse)	Huntington's disease carotid artery disease congestive heart failure diabetic neuropathy end stage renal disease hypertension hypothyroidism metabolic dysfunction-associated steatotic liver disease obesity obstructive jaundice polycystic liver disease steatotic liver disease transient cerebral ischemia type 2 diabetes mellitus
22059	transformation related protein 53	Trp53	Mus musculus (house mouse)	B-lymphoblastic leukemia/lymphoma CHARGE syndrome Graves' disease Leber hereditary optic neuropathy Li-Fraumeni syndrome 1 Li-Fraumeni syndrome T-cell non-Hodgkin lymphoma acute myeloid leukemia adenoid cystic carcinoma aggressive NK-cell leukemia angiosarcoma basal cell carcinoma breast cancer bronchiolo-alveolar adenocarcinoma bronchopulmonary dysplasia cancer cervical adenocarcinoma cervical squamous cell carcinoma cholesteatoma of middle ear choroid plexus papilloma clear cell renal cell carcinoma colorectal adenocarcinoma colorectal cancer colorectal carcinoma coronary artery disease coronary restenosis diffuse large B-cell lymphoma dilated cardiomyopathy disease of cellular proliferation ductal carcinoma in situ dyskeratosis congenita endometrial adenocarcinoma endometrial cancer endometrial carcinoma esophagus squamous cell carcinoma gastric adenocarcinoma glioblastoma graft-versus-host disease hematologic cancer hepatocellular carcinoma high grade glioma ischemia leukemia low tension glaucoma lung non-small cell carcinoma malignant peripheral nerve sheath tumor medulloblastoma melanoma meninges sarcoma mismatch repair cancer syndrome multiple myeloma myelodysplastic syndrome myelofibrosis nasal cavity cancer nasopharynx carcinoma oral mucosa leukoplakia oral squamous cell carcinoma oral submucous fibrosis osteosarcoma ovary serous adenocarcinoma pancreatic cancer pancreatic intraductal papillary-mucinous neoplasm paranasal sinus benign neoplasm pre-malignant neoplasm primary open angle glaucoma prostate cancer pterygium renal cell carcinoma sarcoma serous cystadenocarcinoma squamous cell carcinoma stomach cancer testicular cancer thyroid gland papillary carcinoma tongue squamous cell carcinoma transitional cell carcinoma traumatic brain injury urinary bladder cancer vascular dementia
21991	triosephosphate isomerase 1	Tpi1	Mus musculus (house mouse)	cancer carbohydrate metabolic disorder neurodegenerative disease ocular hypertension triosephosphate isomerase deficiency
21951	tankyrase, TRF1-interacting ankyrin-related ADP-ribose polymerase	Tnks	Mus musculus (house mouse)

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