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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 **1126 - 1150** of **393515** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
22271	uridine phosphorylase 1	Upp1	Mus musculus (house mouse)	middle cerebral artery infarction
22278	upstream transcription factor 1	Usf1	Mus musculus (house mouse)	cardiovascular system disease type 2 diabetes mellitus
22619	sialic acid acetylesterase	Siae	Mus musculus (house mouse)	autoimmune disease
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
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
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
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
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
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
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
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
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
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
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
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
22934	ribose 5-phosphate isomerase A	RPIA	Homo sapiens (human)	Chagas disease agnosia cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital nystagmus critical illness polyneuropathy disease of metabolism dissociated nystagmus epilepsy familial adenomatous polyposis 1 familial adenomatous polyposis hepatocellular carcinoma inflammatory and toxic neuropathy islet cell tumor large intestine cancer liver cancer liver carcinoma meningoencephalitis multiple myeloma neuropathy optic atrophy papillary adenocarcinoma papillary renal cell carcinoma pathologic nystagmus peripheral nervous system disease polyneuropathy spontaneous ocular nystagmus thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland medullary carcinoma thyroid gland papillary carcinoma trypanosomiasis visual epilepsy
23007	phospholipase C eta 1	PLCH1 Aliases: 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase eta-1 DKFZp434C1372 KIAA1069 MGC117152 PLCeta1	Homo sapiens (human)	bronchus cancer bronchus carcinoma colon cancer colonic benign neoplasm colorectal cancer holoprosencephaly idiopathic scoliosis large intestine cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma squamous cell carcinoma tongue squamous cell carcinoma
23038	WD and tetratricopeptide repeats 1	WDTC1	Homo sapiens (human)	obesity
23098	sterile alpha and TIR motif containing 1	SARM1 Aliases: KIAA0524 SAMD2 SARM	Homo sapiens (human)	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease alternating hemiplegia of childhood amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis type 6 amyotrophic lateral sclerosis anterior horn cell disease autonomic neuropathy autosomal recessive distal hereditary motor neuronopathy 1 bacterial sepsis central nervous system disease chronic obstructive pulmonary disease disease of metabolism frontotemporal dementia late onset Parkinson's disease lateral sclerosis motor neuron disease nervous system disease neurodegenerative disease neuropathy peripheral nervous system disease polyneuropathy progressive muscular atrophy prostate cancer prostate carcinoma steatotic liver disease stomach cancer stomach carcinoma substance abuse substance-related disorder
23127	collagen beta(1-O)galactosyltransferase 2	COLGALT2 Aliases: KIAA0584 Procollagen galactosyltransferase	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 bone osteosarcoma breast cancer cerebral degeneration hepatitis A hepatitis lung benign neoplasm osteoarthritis osteosarcoma
23169	solute carrier family 35 member D1	SLC35D1 Aliases: KIAA0260 UDP-glucuronic acid/UDP-N-acetylgalactosamine transporter UGTREL7	Homo sapiens (human)	cleft palate cryptorchidism dermatitis elephantiasis fibrochondrogenesis isolated cleft palate lymphedema mucopolysaccharidosis IV multiple epiphyseal dysplasia osteochondrodysplasia polyhydramnios schneckenbecken dysplasia
23171	glycerol-3-phosphate dehydrogenase 1 like	GPD1L Aliases: KIAA0089	Homo sapiens (human)	Brugada syndrome 1 Brugada syndrome 2 Brugada syndrome 3 Brugada syndrome 4 Brugada syndrome 5 Brugada syndrome 6 Brugada syndrome 7 Brugada syndrome 8 Brugada syndrome 9 Brugada syndrome arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atrial fibrillation congestive heart failure coronary artery disease head and neck squamous cell carcinoma nutmeg liver osteoarthritis sick sinus syndrome steatotic liver disease sudden infant death syndrome
23175	lipin 1	LPIN1 Aliases: KIAA0188 phosphatidate phosphatase LPIN1	Homo sapiens (human)	46,XY sex reversal 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 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 3 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 Pearson syndrome Richter's syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute kidney failure adrenoleukodystrophy agenesis of the corpus callosum with peripheral neuropathy breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease cervix uteri carcinoma in situ chronic kidney disease chronic lymphocytic leukemia colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 diabetes mellitus diabetic ketoacidosis embryoma end stage renal disease essential hypertension familial periodic paralysis fibromyalgia gastroenteritis gestational diabetes glucose intolerance heart disease hepatoblastoma hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hyperinsulinism hypertension ileitis ileocolitis isolated elevated serum creatine phosphokinase levels large intestine cancer lipid metabolism disorder lipoatrophic diabetes mellitus lipodystrophy liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma middle cerebral artery infarction morbid obesity motor peripheral neuropathy myoglobinuria myopathy myositis neuropathy obesity obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum peripheral nervous system disease polycystic ovary syndrome polyneuropathy prediabetes syndrome prostate cancer prostate carcinoma retinitis pigmentosa 9 sarcomatoid carcinoma steatotic liver disease type 2 diabetes mellitus very long chain acyl-CoA dehydrogenase deficiency
23193	glucosidase II alpha subunit	GANAB Aliases: G2AN GIIA GluII KIAA0088 neutral alpha-glucosidase AB	Homo sapiens (human)	Meckel syndrome arthritis arthropathy autosomal dominant polycystic kidney disease chronic fatigue syndrome encephalitis encephalomyelitis gallbladder disease liver disease multiple sclerosis myelitis osteoarthritis polycystic kidney disease 1 polycystic kidney disease 2 polycystic kidney disease 3 polycystic kidney disease polycystic liver disease
23205	acyl-CoA synthetase bubblegum family member 1	ACSBG1 Aliases: BG1 BGM FLJ30320 KIAA0631 MGC14352 bubblegum hBG1 hsBG lipidosin very long-chain acyl-CoA synthetase	Homo sapiens (human)	B-cell lymphoma Clostridium difficile colitis Crohn's colitis Crohn's disease Evans' syndrome HCL-V 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 Langerhans-cell histiocytosis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Richter's syndrome adrenoleukodystrophy autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome autoimmune thrombocytopenic purpura breast adenocarcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer central nervous system lymphoma chronic kidney disease chronic lymphocytic leukemia colitis colon carcinoma colorectal cancer diffuse large B-cell lymphoma embryoma gastroenteritis gliosarcoma hairy cell leukemia hemophagocytic lymphohistiocytosis hepatocellular carcinoma high grade glioma ileitis ileocolitis ileus immune system disease inflammatory bowel disease 1 inflammatory bowel disease intestinal obstruction irritable bowel syndrome kwashiorkor late onset Parkinson's disease liver cancer long QT syndrome lung benign neoplasm lung cancer lung carcinoma lymphoma lymphoplasmacytic lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 macroglobulinemia marasmus mixed glioma multiple myeloma mycosis fungoides neurocirculatory asthenia neurodegenerative disease non-Hodgkin lymphoma nutrition disease obsolete lymphoplasmacytic lymphoma obsolete ymphosarcoma primary immunodeficiency disease protein-energy malnutrition reticulosarcoma rheumatoid arthritis scleroderma systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic scleroderma ulcerative colitis viral infectious disease

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GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

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