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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 **1826 - 1850** of **393515** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
57171	dolichyldiphosphatase 1	DOLPP1 Aliases: LSFR2 linked to Surfeit genes in Fugu rubripes 2	Homo sapiens (human)	endometrial cancer endometrial carcinoma uterine corpus cancer
57214	cell migration inducing hyaluronidase 1	CEMIP Aliases: HYBID IR2155535 TMEM2L hyaluronan-binding protein involved in hyaluronan depolymerization	Homo sapiens (human)	acute myeloid leukemia adenocarcinoma adenoma arthritis arthropathy breast cancer breast carcinoma cancer chromophobe renal cell carcinoma chronic fatigue syndrome clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart cribriform carcinoma embryoma encephalitis encephalomyelitis familial adenomatous polyposis 2 familial retinoblastoma follicular adenoma granular cell carcinoma hepatocellular carcinoma idiopathic interstitial pneumonia idiopathic pulmonary fibrosis large intestine cancer liver cancer lung cancer lung non-small cell carcinoma microcystic adenoma microphthalmia multiple sclerosis myelitis nonpapillary renal cell carcinoma obsolete Matthew-Wood syndrome osteoarthritis ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma pneumonia prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma retinoblastoma rheumatoid arthritis sarcomatoid renal cell carcinoma stomach cancer stomach carcinoma thyroid gland papillary carcinoma trilateral retinoblastoma tubular adenocarcinoma
57223	protein phosphatase 4 regulatory subunit 3B	PPP4R3B	Homo sapiens (human)
57370	UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 3	B4galt3	Mus musculus (house mouse)
57377	mannosyl-oligosaccharide glucosidase	Mogs	Mus musculus (house mouse)	congenital disorder of glycosylation type IIb
57452	polypeptide N-acetylgalactosaminyltransferase 16	GALNT16 Aliases: GalNAc-T16 KIAA1130 polypeptide GalNAc transferase 16	Homo sapiens (human)	breast cancer breast carcinoma idiopathic scoliosis
57462	myogenesis regulating glycosidase (putative)	MYORG Aliases: NET37	Homo sapiens (human)	amnestic disorder basal ganglia calcification choreatic disease dystonia epilepsy hydrocephalus lingual-facial-buccal dyskinesia microcephaly migraine neurodegenerative disease placental insufficiency recurrent corneal erosion retrograde amnesia secondary Parkinson disease syndromic X-linked intellectual disability type 10 thrombocytopenia visual epilepsy
57511	component of oligomeric golgi complex 6	COG6 Aliases: COD2 KIAA1134	Homo sapiens (human)	Gilbert syndrome acquired hyperkeratosis allergic asthma anemia anhidrosis asthma bilirubin metabolic disorder blood coagulation disease cerebral degeneration cholestasis congenital disorder of glycosylation type II congenital disorder of glycosylation type IIl congenital disorder of glycosylation coronary artery disease dental caries dental enamel hypoplasia dentin caries developmental and epileptic encephalopathy 36 epilepsy gastroenteritis gastrointestinal system disease hydrocephalus hypohidrosis intellectual disability intestinal disease intrinsic asthma juvenile rheumatoid arthritis learning disability leiomyoma macrocytic anemia microcephaly myofibroma nonepidermolytic palmoplantar keratoderma palmoplantar keratosis pancytopenia parapsoriasis placental insufficiency primary biliary cholangitis primary immunodeficiency disease proctitis psoriasis pustulosis of palm and sole rheumatoid arthritis systemic lupus erythematosus thrombocytopenia uterine fibroid visual epilepsy
57678	glycerol-3-phosphate acyltransferase, mitochondrial	GPAM Aliases: GPAT1 KIAA1560 MGC26846 glycerol-3-phosphate acyltransferase 1, mitochondrial	Homo sapiens (human)	cancer embryoma familial nephrotic syndrome lipoid nephrosis melanoma metabolic dysfunction-associated steatotic liver disease nephrotic syndrome obesity overnutrition skin melanoma steatotic liver disease
57704	glucosylceramidase beta 2	GBA2 Aliases: AD035 DKFZp762K054 KIAA1605 bile acid beta-glucosidase glucocerebrosidase 2 non-lysosomal glucosylceramidase	Homo sapiens (human)	Charcot-Marie-Tooth disease type 5 Gaucher's disease Henoch-Schoenlein purpura Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease MASA syndrome Mast syndrome Niemann-Pick disease type C1 Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease SPOAN syndrome Troyer syndrome alternating hemiplegia of childhood autonomic neuropathy cancer cataract central nervous system disease cerebellar ataxia cerebellar disease cerebral degeneration congenital nystagmus cystic fibrosis dementia dissociated nystagmus glaucoma hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia hypersensitivity vasculitis infertility intellectual disability learning disability male infertility nervous system disease paraplegia pathologic nystagmus scoliosis sensorineural hearing loss spontaneous ocular nystagmus trichohepatoenteric syndrome 1 trichohepatoenteric syndrome
57733	glucosylceramidase beta 3 (gene/pseudogene)	GBA3 Aliases: CBGL1 GLUC KLrP cytosolic β-glucosidase-like protein-1 klotho-related protein	Homo sapiens (human)	Gaucher's disease type I Gaucher's disease Goodpasture syndrome Takayasu's arteritis West Nile fever allergic asthma asthma cancer cystic fibrosis diabetic ketoacidosis granulomatosis with polyangiitis hepatocellular carcinoma kidney disease liver cancer obsolete type 1 diabetes mellitus 9 polyarteritis nodosa stomach cancer stomach carcinoma substance abuse substance-related disorder 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
57818	glucose-6-phosphatase catalytic subunit 2	G6PC2 Aliases: IGRP islet specific glucose 6 phosphatase catalytic subunit related protein	Homo sapiens (human)	Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 breast cancer breast carcinoma cystinuria diabetes mellitus diabetic ketoacidosis galactosemia gestational diabetes glucose intolerance 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 hyperglycemia hyperinsulinism insulinoma obsolete type 1 diabetes mellitus 9 prediabetes syndrome 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
58193	exostosin-like glycosyltransferase 2	Extl2	Mus musculus (house mouse)
58200	protein phosphatase 1, regulatory inhibitor subunit 1A	Ppp1r1a	Mus musculus (house mouse)
58250	carbohydrate sulfotransferase 11	Chst11	Mus musculus (house mouse)
58530	lymphocyte antigen 6 family member G6D	LY6G6D Aliases: G6D LY6-D Ly6-D MEGT1 NG25	Homo sapiens (human)	B-cell lymphoma Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma diabetic ketoacidosis large intestine cancer nonpapillary renal cell carcinoma obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid renal cell carcinoma 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
58810	aldo-keto reductase family 1, member A1	Akr1a1	Mus musculus (house mouse)	breast cancer lung adenocarcinoma
58866	trehalase (brush-border membrane glycoprotein)	Treh	Mus musculus (house mouse)
58924	fucosyltransferase 2	Fut2	Rattus norvegicus (Norway rat)	vitamin B12 deficiency
58977	protein phosphatase 1, regulatory (inhibitor) subunit 1A	Ppp1r1a	Rattus norvegicus (Norway rat)
59027	nicotinamide phosphoribosyltransferase	Nampt	Mus musculus (house mouse)	carotid artery disease coronary artery disease kidney failure metabolic dysfunction-associated steatotic liver disease middle cerebral artery infarction obesity periodontitis psoriasis pulmonary hypertension transient cerebral ischemia type 2 diabetes mellitus
59031	carbohydrate sulfotransferase 12	Chst12	Mus musculus (house mouse)	hypertension
59048	C1GALT1-specific chaperone 1	C1galt1c1	Mus musculus (house mouse)	Tn polyagglutination syndrome hemolytic-uremic syndrome
59167	Olfactory-specific 9	OS9	Drosophila melanogaster (fruit fly)
59320	adenylate cyclase 10	Adcy10	Rattus norvegicus (Norway rat)

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