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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 **7376 - 7400** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▲	Organism	Disease Ontology
5993	regulatory factor X5	RFX5	Homo sapiens (human)
64864	regulatory factor X7	RFX7	Homo sapiens (human)
57139	ral guanine nucleotide dissociation stimulator like 3	RGL3	Homo sapiens (human)
56963	repulsive guidance molecule BMP co-receptor a	RGMA Aliases: RGM	Homo sapiens (human)	Mycobacterium avium complex disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease basal cell carcinoma breast cancer bronchiectasis cancer chronic fatigue syndrome chronic kidney disease complex partial epilepsy cone-rod dystrophy 2 cone-rod dystrophy cystic fibrosis disease of mental health embryoma encephalitis encephalomyelitis epilepsy hemochromatosis type 2 hemochromatosis type 2A hemochromatosis heroin dependence lesion of sciatic nerve lung disease middle cerebral artery infarction morphine dependence multiple sclerosis myelitis neuromyelitis optica obesity opiate dependence primary progressive multiple sclerosis progressive relapsing multiple sclerosis prostate cancer prostate carcinoma psychotic disorder sciatic neuropathy secondary progressive multiple sclerosis temporal lobe epilepsy visual epilepsy
285704	repulsive guidance molecule BMP co-receptor b	RGMB Aliases: DRAGON FLJ90406	Homo sapiens (human)	allergic asthma asthma atrial fibrillation brain stem infarction breast cancer cancer cerebral artery occlusion cerebral infarction cerebrovascular disease colorectal cancer colorectal carcinoma embryoma hemochromatosis type 2 hemochromatosis type 2A hemochromatosis hepatocellular carcinoma intrinsic asthma large intestine cancer liver cancer lung cancer lung non-small cell carcinoma middle cerebral artery infarction multiple sclerosis prostate cancer prostate carcinoma rheumatoid arthritis
9104	regucalcin	RGN Aliases: RC SMP30 gluconolactonase senescence marker protein-30	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 Becker muscular dystrophy Duchenne muscular dystrophy Pick's disease Reye syndrome adenocarcinoma adenoma argininosuccinic aciduria 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 breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cataract cerebral degeneration cervical adenocarcinoma cervix carcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease cribriform carcinoma depressive disorder diarrhea distal myopathy dry eye syndrome dysthymic disorder embryoma endomyocardial fibrosis essential hypertension facioscapulohumeral muscular dystrophy familial hyperlipidemia gallbladder disease gastroenteritis glomerulonephritis granular cell carcinoma hepatitis B hepatitis hepatoblastoma hepatocellular carcinoma hypertension ileitis ileocolitis invasive ductal carcinoma kidney cancer kidney disease kidney failure large intestine cancer limb-girdle muscular dystrophy liver cancer liver carcinoma liver cirrhosis liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder male infertility melancholic depression muscular dystrophy nephritis nephrosis neuropathy neurotic disorder nonpapillary renal cell carcinoma 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 oculopharyngeal muscular dystrophy osteomalacia pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma peripheral nervous system disease polyneuropathy prostate cancer prostate carcinoma pulmonary emphysema pyoureter renal carcinoma renal cell carcinoma rhabdomyosarcoma rickets sarcomatoid renal cell carcinoma scurvy stomach cancer tubular adenocarcinoma uremia vascular dementia vitelliform macular dystrophy xerophthalmia
400966	RANBP2 like and GRIP domain containing 1	RGPD1	Homo sapiens (human)
653489	RANBP2 like and GRIP domain containing 3	RGPD3	Homo sapiens (human)
285190	RANBP2 like and GRIP domain containing 4	RGPD4	Homo sapiens (human)
84220	RANBP2 like and GRIP domain containing 5	RGPD5	Homo sapiens (human)
729540	RANBP2 like and GRIP domain containing 6	RGPD6	Homo sapiens (human)
727851	RANBP2 like and GRIP domain containing 8	RGPD8	Homo sapiens (human)
5995	retinal G protein coupled receptor	RGR	Homo sapiens (human)
5996	regulator of G protein signaling 1	RGS1	Homo sapiens (human)
5998	regulator of G protein signaling 3	RGS3	Homo sapiens (human)
85397	regulator of G protein signaling 8	RGS8	Homo sapiens (human)
6005	Rh associated glycoprotein	RHAG	Homo sapiens (human)
57414	rhomboid domain containing 2	RHBDD2	Homo sapiens (human)
64285	rhomboid 5 homolog 1	RHBDF1	Homo sapiens (human)
79651	rhomboid 5 homolog 2	RHBDF2	Homo sapiens (human)
57127	Rh family B glycoprotein	RHBG	Homo sapiens (human)
51458	Rh family C glycoprotein	RHCG	Homo sapiens (human)
6009	Ras homolog, mTORC1 binding	RHEB	Homo sapiens (human)
6010	rhodopsin	RHO	Homo sapiens (human)
387	ras homolog family member A	RHOA Aliases: RHOH12 Rho12	Homo sapiens (human)

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