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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 **8376 - 8400** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
126792	beta-1,3-galactosyltransferase 6	B3GALT6 Aliases: beta-1,3-galactosyltransferase-6 beta3GalT6	Homo sapiens (human)	Ehlers-Danlos syndrome spondylodysplastic type 2 Ehlers-Danlos syndrome Hailey-Hailey disease Hirschsprung's disease Laron syndrome Rothmund-Thomson syndrome achondroplasia aortic valve disease 1 aortic valve disease 2 aortic valve stenosis atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB bicuspid aortic valve disease bone disease cartilage disease cherubism chondrodysplasia punctata chromophobe renal cell carcinoma clear cell renal cell carcinoma cleft palate clubfoot collagen disease collecting duct carcinoma connective tissue disease cutis laxa enophthalmos exostosis heart septal defect hepatocellular carcinoma intellectual disability isolated cleft palate isolated ectopia lentis learning disability liver cancer mal de Meleda mitral valve insufficiency mitral valve prolapse myopia nonpapillary renal cell carcinoma obsolete exophthalmos orbital disease osteogenesis imperfecta osteoporosis papillary renal cell carcinoma paraplegia patent foramen ovale periarthritis renal carcinoma renal cell carcinoma restrictive dermopathy sarcomatoid renal cell carcinoma scoliosis spinal cord disease spondyloepimetaphyseal dysplasia with joint laxity type 1 tendinitis ventricular septal defect
126820	dynein axonemal intermediate chain 3	DNAI3	Homo sapiens (human)
126868	mab-21 like 3	MAB21L3	Homo sapiens (human)
126969	solute carrier family 44 member 3	SLC44A3	Homo sapiens (human)
127059	olfactory receptor family 2 subfamily M member 5	OR2M5	Homo sapiens (human)
127062	olfactory receptor family 2 subfamily M member 3	OR2M3	Homo sapiens (human)
127064	olfactory receptor family 2 subfamily T member 12	OR2T12	Homo sapiens (human)
127066	olfactory receptor family 14 subfamily C member 36	OR14C36	Homo sapiens (human)
127068	olfactory receptor family 2 subfamily T member 34	OR2T34	Homo sapiens (human)
127069	olfactory receptor family 2 subfamily T member 10	OR2T10	Homo sapiens (human)
127074	olfactory receptor family 2 subfamily T member 4	OR2T4	Homo sapiens (human)
127077	olfactory receptor family 2 subfamily T member 11	OR2T11	Homo sapiens (human)
127255	leucine rich repeats and IQ motif containing 3	LRRIQ3	Homo sapiens (human)
127281	peroxiredoxin like 2B	PRXL2B Aliases: MGC26818 prostamide/prostaglandin F synthase thioredoxin-type PGF synthase	Homo sapiens (human)
127294	myomesin 3	MYOM3	Homo sapiens (human)
127343	diencephalon/mesencephalon homeobox 1	DMBX1	Homo sapiens (human)
127385	olfactory receptor family 10 subfamily J member 5	OR10J5	Homo sapiens (human)
127396	zinc finger protein 684	ZNF684	Homo sapiens (human)
127435	podocan	PODN	Homo sapiens (human)
127550	alpha 1,3-galactosyltransferase 2	A3GALT2 Aliases: IGB3S IGBS3S iGb3 synthase isoglobotriaosylceramide synthase	Homo sapiens (human)
127579	DC-STAMP domain containing 2	DCST2	Homo sapiens (human)
127602	dynein axonemal heavy chain 14	DNAH14	Homo sapiens (human)
127623	olfactory receptor family 2 subfamily B member 11	OR2B11	Homo sapiens (human)
127665	zinc finger protein 648	ZNF648	Homo sapiens (human)
127707	kelch domain containing 7A	KLHDC7A	Homo sapiens (human)

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