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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 **6076 - 6100** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
54209	triggering receptor expressed on myeloid cells 2	TREM2	Homo sapiens (human)
54210	triggering receptor expressed on myeloid cells 1	TREM1	Homo sapiens (human)
54221	syntrophin gamma 2	SNTG2	Homo sapiens (human)
54328	G protein-coupled receptor 173	GPR173	Homo sapiens (human)
54329	G protein-coupled receptor 85	GPR85	Homo sapiens (human)
54344	dolichyl-phosphate mannosyltransferase subunit 3, regulatory	DPM3 Aliases: DPM synthase complex subunit MGC125904 MGC125905 MGC34275	Homo sapiens (human)	Duchenne muscular dystrophy autosomal dominant Emery-Dreifuss muscular dystrophy 2 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 cardiomyopathy clubfoot congenital disorder of glycosylation type I congenital muscular dystrophy distal myopathy endomyocardial fibrosis facioscapulohumeral muscular dystrophy hypertrophic cardiomyopathy isolated elevated serum creatine phosphokinase levels limb-girdle muscular dystrophy muscular dystrophy-dystroglycanopathy type B15 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 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 oculopharyngeal muscular dystrophy rippling muscle disease 2
54346	unc-93 homolog A	UNC93A	Homo sapiens (human)
54361	Wnt family member 4	WNT4	Homo sapiens (human)
54363	hydroxyacid oxidase 1	HAO1 Aliases: GOX glycolate oxidase 1	Homo sapiens (human)	familial hyperinsulinemic hypoglycemia 1 familial hyperinsulinemic hypoglycemia 2 hyperinsulinemic hypoglycemia inherited metabolic disorder nephrolithiasis primary hyperoxaluria prostate cancer prostate carcinoma uric acid nephrolithiasis
54386	TERF2 interacting protein	TERF2IP	Homo sapiens (human)
54407	solute carrier family 38 member 2	SLC38A2	Homo sapiens (human)
54413	neuroligin 3	NLGN3	Homo sapiens (human)
54414	sialic acid acetylesterase	SIAE	Homo sapiens (human)	autoimmune disease
54429	taste 2 receptor member 5	TAS2R5	Homo sapiens (human)
54431	DnaJ heat shock protein family (Hsp40) member C10	DNAJC10	Homo sapiens (human)
54432	Yip1 domain family member 1	YIPF1	Homo sapiens (human)
54437	semaphorin 5B	SEMA5B	Homo sapiens (human)
54439	RNA binding motif protein 27	RBM27	Homo sapiens (human)
54443	anillin, actin binding protein	ANLN	Homo sapiens (human)
54455	F-box protein 42	FBXO42	Homo sapiens (human)
54456	Mov10 like RNA helicase 1	MOV10L1	Homo sapiens (human)
54461	F-box and WD repeat domain containing 5	FBXW5	Homo sapiens (human)
54462	coiled-coil serine rich protein 2	CCSER2	Homo sapiens (human)
54463	reticulophagy regulator 1	RETREG1	Homo sapiens (human)
54464	5'-3' exoribonuclease 1	XRN1	Homo sapiens (human)

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