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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	October 29, 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 **6276 - 6300** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
6195	ribosomal protein S6 kinase A1	RPS6KA1	Homo sapiens (human)
7423	vascular endothelial growth factor B	VEGFB	Homo sapiens (human)
54578	UDP glucuronosyltransferase family 1 member A6	UGT1A6 Aliases: GNT1 HLUGP UGT1F	Homo sapiens (human)	Crigler-Najjar syndrome Gaucher's disease Gilbert syndrome abdominal obesity-metabolic syndrome 1 adenocarcinoma adenoma agranulocytosis allergic asthma alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia arteriosclerotic cardiovascular disease asthma atherosclerosis beta thalassemia bilirubin metabolic disorder bladder carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiac arrest cardiovascular system disease childhood acute lymphocytic leukemia cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chronic myeloid leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma contact dermatitis coronary artery disease cryptococcosis cystinuria diabetes mellitus diarrhea differentiated thyroid gland carcinoma embryoma epilepsy female reproductive organ cancer follicular adenoma galactosemia gallbladder disease gastritis glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease Ia glycogen storage disease head and neck cancer head and neck squamous cell carcinoma heart disease hemoglobin H disease hepatitis B hepatitis D hepatocellular carcinoma hereditary spherocytosis influenza intrinsic asthma kernicterus due to isoimmunization kernicterus large intestine cancer leukopenia liver cancer liver disease lung benign neoplasm lung cancer lung carcinoma microcystic adenoma neonatal jaundice neutropenia nodular prostate nutmeg liver obesity occupational dermatitis papillary adenoma prostate cancer prostate carcinoma prostatic adenoma rheumatoid arthritis sarcomatoid carcinoma severe congenital neutropenia sickle cell anemia status epilepticus steatotic liver disease stomach cancer stomach carcinoma thalassemia type 2 diabetes mellitus urinary bladder cancer visual epilepsy xeroderma pigmentosum group D
64106	neuropeptide FF receptor 1	NPFFR1	Homo sapiens (human)
3784	potassium voltage-gated channel subfamily Q member 1	KCNQ1	Homo sapiens (human)	Jervell-Lange Nielsen syndrome atrial fibrillation familial atrial fibrillation hypertension long QT syndrome 1 long QT syndrome seminoma short QT syndrome type 2 diabetes mellitus
64838	fibronectin type III domain containing 4	FNDC4	Homo sapiens (human)
116255	monoacylglycerol O-acyltransferase 1	MOGAT1 Aliases: DGAT2L MGAT1	Homo sapiens (human)	multiple sclerosis overnutrition steatotic liver disease
7039	transforming growth factor alpha	TGFA	Homo sapiens (human)
5976	UPF1 RNA helicase and ATPase	UPF1	Homo sapiens (human)
23062	golgi associated, gamma adaptin ear containing, ARF binding protein 2	GGA2	Homo sapiens (human)
54480	chondroitin polymerizing factor 2	CHPF2 Aliases: CSGlcA-T ChSy-3 KIAA1402 chondroitin sulfate glucuronyltransferase	Homo sapiens (human)	cancer colorectal cancer colorectal carcinoma embryoma large intestine cancer
10695	canopy FGF signaling regulator 3	CNPY3	Homo sapiens (human)
4706	NADH:ubiquinone oxidoreductase subunit AB1	NDUFAB1 Aliases: ACP ACP1 FASN2A SDAP acyl carrier protein, mitochondrial complex I SDAP subunit	Homo sapiens (human)	Alzheimer's disease HCL-V Lynch syndrome Marfan syndrome Richter's syndrome Wilson disease X-linked dilated cardiomyopathy actinic keratosis adamantinous craniopharyngioma adult lymphoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease ataxic cerebral palsy atherosclerosis brain cancer cancer central nervous system lymphoma central retinal vein occlusion cerebral infarction cerebrovascular disease childhood lymphoma chronic lymphocytic leukemia congenital hemolytic anemia congestive heart failure coronary artery disease craniopharyngioma cystinuria dementia dental caries dentin sensitivity 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 endometrial cancer endometrial carcinoma favism galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease gonorrhea hairy cell leukemia hemochromatosis hereditary elliptocytosis iron metabolism disease lymphoma neurodegeneration with brain iron accumulation neurodegenerative disease nutmeg liver obesity obsolete ymphosarcoma osteoporosis papillary craniopharyngioma root caries situs inversus trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberculosis tuberous sclerosis uterine corpus cancer
23516	solute carrier family 39 member 14	SLC39A14	Homo sapiens (human)	hypermanganesemia with dystonia 2
55032	solute carrier family 35 member A5	SLC35A5 Aliases: FLJ20730	Homo sapiens (human)
137797	LY6/PLAUR domain containing 2	LYPD2 Aliases: RGTR430 UNQ430	Homo sapiens (human)
647174	serpin family E member 3	SERPINE3	Homo sapiens (human)
57649	PHD finger protein 12	PHF12	Homo sapiens (human)
8001	glycine receptor alpha 3	GLRA3	Homo sapiens (human)
47	ATP citrate lyase	ACLY Aliases: ACL ATP citrate synthase ATPCL CLATP	Homo sapiens (human)	Behcet's disease Zollinger-Ellison syndrome abdominal aortic aneurysm acute myeloid leukemia adult oligodendroglioma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiac arrest cardiovascular system disease childhood oligodendroglioma childhood osteosarcoma chromophobe renal cell carcinoma chronic kidney disease chronic obstructive pulmonary disease clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease diabetes mellitus disease of metabolism embryoma enthesopathy exostosis familial hyperlipidemia heart disease hepatocellular carcinoma high grade glioma hyperinsulinism inclusion body myositis kwashiorkor large intestine cancer liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma marasmus mast-cell leukemia mastocytosis mixed oligodendroglioma-astrocytoma 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 nonpapillary renal cell carcinoma nutrition disease obesity oligodendroglioma osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma papillary renal cell carcinoma periarthritis polycystic kidney disease 3 prostate cancer prostate carcinoma protein-energy malnutrition renal carcinoma renal cell carcinoma renal osteodystrophy sarcomatoid renal cell carcinoma septic arthritis squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma synovitis tendinitis tenosynovitis tongue squamous cell carcinoma trigeminal neuralgia type 2 diabetes mellitus
116841	synaptosome associated protein 47	SNAP47	Homo sapiens (human)
121355	gametocyte specific factor 1	GTSF1	Homo sapiens (human)
187	apelin receptor	APLNR	Homo sapiens (human)
5336	phospholipase C gamma 2	PLCG2	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 Burkitt lymphoma CINCA Syndrome Creutzfeldt-Jakob disease Crohn's colitis Crohn's disease Hailey-Hailey disease Lewy body dementia Muckle-Wells syndrome Pick's disease Reye syndrome Richter's syndrome Rothmund-Thomson syndrome acute lymphoblastic leukemia acute myeloid leukemia adenosarcoma age related macular degeneration allergic rhinitis angioedema autoimmune disease autoimmune lymphoproliferative syndrome autoimmune thyroiditis autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB bone osteosarcoma breast cancer breast carcinoma bronchiolitis cancer candidiasis cellulitis central nervous system lymphoma cerebral degeneration cherubism childhood osteosarcoma childhood type dermatomyositis chronic lymphocytic leukemia coronary artery disease cutis laxa degeneration of macula and posterior pole dermatomyositis diffuse large B-cell lymphoma embryoma exostosis familial adenomatous polyposis 1 familial adenomatous polyposis familial cold autoinflammatory syndrome 1 familial cold autoinflammatory syndrome 3 familial cold autoinflammatory syndrome 4 familial cold autoinflammatory syndrome granuloma annulare hepatocellular carcinoma immune system disease inflammatory bowel disease 1 inflammatory bowel disease interstitial lung disease islet cell tumor kidney cancer leukemia lipoid nephrosis liver cancer lymphoma lymphoplasmacytic lymphoma macroglobulinemia macular degeneration mal de Meleda nephroblastoma neurodegenerative disease obsolete lymphoplasmacytic lymphoma obsolete ymphosarcoma oral candidiasis osteoporosis osteosarcoma progressive supranuclear palsy restrictive dermopathy rheumatoid arthritis stomach cancer thrombophilia ulcerative colitis urticaria vasomotor rhinitis vitiligo
1310	collagen type XIX alpha 1 chain	COL19A1	Homo sapiens (human)

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