GlyCosmos Portal

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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 **8251 - 8275** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
399979	sorting nexin 19	SNX19	Homo sapiens (human)
64434	nucleolar protein with MIF4G domain 1	NOM1	Homo sapiens (human)
8697	cell division cycle 23	CDC23	Homo sapiens (human)
55117	solute carrier family 6 member 15	SLC6A15	Homo sapiens (human)
5754	protein tyrosine kinase 7 (inactive)	PTK7	Homo sapiens (human)
9604	ring finger protein 14	RNF14	Homo sapiens (human)
114818	kelch like family member 29	KLHL29	Homo sapiens (human)
57524	CASK interacting protein 1	CASKIN1	Homo sapiens (human)
26470	seizure related 6 homolog like 2	SEZ6L2	Homo sapiens (human)
27439	transmembrane protein 121B	TMEM121B	Homo sapiens (human)
8218	clathrin heavy chain like 1	CLTCL1	Homo sapiens (human)
80712	ESX homeobox 1	ESX1	Homo sapiens (human)
23136	erythrocyte membrane protein band 4.1 like 3	EPB41L3	Homo sapiens (human)
53829	purinergic receptor P2Y13	P2RY13	Homo sapiens (human)
284415	V-set and transmembrane domain containing 1	VSTM1	Homo sapiens (human)
8526	diacylglycerol kinase epsilon	DGKE Aliases: DAGK6 DGK	Homo sapiens (human)	Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease acute kidney failure allergic asthma asthma atypical hemolytic-uremic syndrome breast cancer cancer capillary disease cardiovascular system disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cone-rod dystrophy embryoma epilepsy familial nephrotic syndrome fundus albipunctatus glomerulonephritis heart disease hemolytic anemia hemolytic-uremic syndrome hereditary hemorrhagic telangiectasia intrinsic asthma kidney disease kidney failure large intestine cancer lipoid nephrosis liver cirrhosis membranoproliferative glomerulonephritis mitochondrial DNA depletion syndrome nephritis nephrosis nephrotic syndrome type 7 nephrotic syndrome obesity proteinuria pyoureter retinitis pigmentosa telangiectasis thrombocytopenia thrombotic thrombocytopenic purpura uremia visual epilepsy
10300	katanin regulatory subunit B1	KATNB1	Homo sapiens (human)
3899	ALF transcription elongation factor 3	AFF3	Homo sapiens (human)
7075	tyrosine kinase with immunoglobulin like and EGF like domains 1	TIE1	Homo sapiens (human)
26290	polypeptide N-acetylgalactosaminyltransferase 8	GALNT8 Aliases: GALNAC-T8 polypeptide GalNAc transferase 8	Homo sapiens (human)	autosomal dominant hypophosphatemic rickets disease of metabolism hepatitis C
1293	collagen type VI alpha 3 chain	COL6A3	Homo sapiens (human)
147323	StAR related lipid transfer domain containing 6	STARD6	Homo sapiens (human)
8819	Sin3A associated protein 30	SAP30	Homo sapiens (human)
134	adenosine A1 receptor	ADORA1	Homo sapiens (human)
80025	pantothenate kinase 2	PANK2	Homo sapiens (human)

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