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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 **1351 - 1375** of **393515** in total

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Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▲
853113	dolichyl-phosphate-mannose-protein mannosyltransferase PMT6	PMT6	Saccharomyces cerevisiae S288C	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy congenital muscular dystrophy-dystroglycanopathy type A2 lissencephaly muscular dystrophy-dystroglycanopathy type B2 muscular dystrophy-dystroglycanopathy muscular dystrophy
100490100	protein-O-mannosyltransferase 2	pomt2	Xenopus tropicalis (tropical clawed frog)	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy congenital muscular dystrophy-dystroglycanopathy type A2 lissencephaly muscular dystrophy-dystroglycanopathy type B2 muscular dystrophy-dystroglycanopathy muscular dystrophy
563878	protein-O-mannosyltransferase 2	pomt2	Danio rerio (zebrafish)	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy congenital muscular dystrophy-dystroglycanopathy type A2 lissencephaly muscular dystrophy-dystroglycanopathy type B2 muscular dystrophy-dystroglycanopathy muscular dystrophy
571876	protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)	pomgnt1	Danio rerio (zebrafish)	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2O congenital muscular dystrophy-dystroglycanopathy type A3 lissencephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B3 muscular dystrophy retinitis pigmentosa
68273	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	Pomgnt1	Mus musculus (house mouse)	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2O congenital muscular dystrophy-dystroglycanopathy type A3 lissencephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B3 muscular dystrophy retinitis pigmentosa
362567	protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)	Pomgnt1	Rattus norvegicus (Norway rat)	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2O congenital muscular dystrophy-dystroglycanopathy type A3 lissencephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B3 muscular dystrophy retinitis pigmentosa
100158594	protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)	pomgnt1	Xenopus tropicalis (tropical clawed frog)	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2O congenital muscular dystrophy-dystroglycanopathy type A3 lissencephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B3 muscular dystrophy retinitis pigmentosa
495292	protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) S homeolog	pomgnt1.S	Xenopus laevis (African clawed frog)	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2O congenital muscular dystrophy-dystroglycanopathy type A3 lissencephaly muscular dystrophy-dystroglycanopathy type B3 muscular dystrophy retinitis pigmentosa
414570	protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) L homeolog	pomgnt1.L	Xenopus laevis (African clawed frog)	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2O congenital muscular dystrophy-dystroglycanopathy type A3 lissencephaly muscular dystrophy-dystroglycanopathy type B3 muscular dystrophy retinitis pigmentosa
299841	ribitol xylosyltransferase 1	Rxylt1	Rattus norvegicus (Norway rat)	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A10
216395	ribitol xylosyltransferase 1	Rxylt1	Mus musculus (house mouse)	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A10
100145540	ribitol xylosyltransferase 1	rxylt1	Xenopus tropicalis (tropical clawed frog)	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A10
557187	ribitol xylosyltransferase 1	rxylt1	Danio rerio (zebrafish)	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A10
100170600	beta-1,4-glucuronyltransferase 1	b4gat1	Xenopus tropicalis (tropical clawed frog)	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A13 muscular dystrophy-dystroglycanopathy type B1
37861	uncharacterized protein	CG3253	Drosophila melanogaster (fruit fly)	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A13 muscular dystrophy-dystroglycanopathy type B1
101669768	beta-1,4-glucuronyltransferase 1	b4gat1	Danio rerio (zebrafish)	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A13 muscular dystrophy-dystroglycanopathy type B1
293667	beta-1,4-glucuronyltransferase 1	B4gat1	Rattus norvegicus (Norway rat)	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A13 muscular dystrophy-dystroglycanopathy type B1
108902	beta-1,4-glucuronyltransferase 1	B4gat1	Mus musculus (house mouse)	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A13 muscular dystrophy-dystroglycanopathy type B1
84317	coiled-coil domain containing 115	CCDC115 Aliases: FLJ30131 MGC12981 ccp1	Homo sapiens (human)	Wilson disease cancer congenital disorder of glycosylation type IIo congenital disorder of glycosylation gallbladder disease hemochromatosis iron metabolism disease liver disease male infertility measles neuroblastoma neurodegenerative disease prostate adenocarcinoma prostate cancer prostate carcinoma
51422	protein kinase AMP-activated non-catalytic subunit gamma 2	PRKAG2	Homo sapiens (human)	Wolff-Parkinson-White syndrome glycogen storage disease hypertrophic cardiomyopathy 6 lethal congenital glycogen storage disease of heart neurodegenerative disease
108099	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	Prkag2	Mus musculus (house mouse)	Wolff-Parkinson-White syndrome glycogen storage disease hypertrophic cardiomyopathy 6 lethal congenital glycogen storage disease of heart neurodegenerative disease
241113	protein kinase, AMP-activated, gamma 3 non-catalytic subunit	Prkag3	Mus musculus (house mouse)	Wolff-Parkinson-White syndrome lethal congenital glycogen storage disease of heart neurodegenerative disease
53632	protein kinase AMP-activated non-catalytic subunit gamma 3	PRKAG3	Homo sapiens (human)	Wolff-Parkinson-White syndrome lethal congenital glycogen storage disease of heart neurodegenerative disease
8435	sterol O-acyltransferase 2	SOAT2 Aliases: ACAT2 acyl-Coenzyme A: cholesterol acyltransferase 2	Homo sapiens (human)	Wolman disease arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cancer celiac disease coronary artery disease end stage renal disease familial hyperlipidemia hepatocellular carcinoma lipid storage disease liver cancer lysosomal acid lipase deficiency nephrotic syndrome nutmeg liver steatotic liver disease
16889	lysosomal acid lipase A	Lipa	Mus musculus (house mouse)	Wolman disease cholesterol ester storage disease lysosomal acid lipase deficiency

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