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 **6351 - 6375** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▼	Disease Ontology
56833	SLAM family member 8	SLAMF8	Homo sapiens (human)
135924	olfactory receptor family 9 subfamily A member 2	OR9A2	Homo sapiens (human)
57496	myocardin related transcription factor B	MRTFB	Homo sapiens (human)
79158	N-acetylglucosamine-1-phosphate transferase subunits alpha and beta	GNPTAB Aliases: KIAA1208 MGC4170	Homo sapiens (human)	Ebola hemorrhagic fever Fabry disease Laron syndrome Legg-Calve-Perthes disease Scheuermann's disease achondroplasia alexia anemia aortic valve insufficiency arrhythmogenic right ventricular cardiomyopathy autistic disorder cancer capillary hemangioma cardiomyopathy cavernous hemangioma chromophobe renal cell carcinoma chylomicron retention disease clear cell renal cell carcinoma clubfoot collecting duct carcinoma congenital central hypoventilation syndrome congestive heart failure corneal dystrophy craniosynostosis disease of metabolism dyslexia embryoma endomyocardial fibrosis enterocele familial hypertrophic cardiomyopathy glycoproteinosis hemangioma hypertrophic cardiomyopathy inguinal hernia intellectual disability keratosis follicularis learning disability lipid storage disease lysosomal storage disease macrocytic anemia megalocornea mixed sleep apnea mongolian spot mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucolipidosis mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis multiple epiphyseal dysplasia nonpapillary renal cell carcinoma obstructive sleep apnea omphalocele osteochondrodysplasia papillary renal cell carcinoma pseudoxanthoma elasticum renal carcinoma renal cell carcinoma retinal degeneration retinal disease retinitis sarcomatoid renal cell carcinoma scoliosis sleep apnea spinal cord disease stuttering syringomyelia umbilical hernia
762	carbonic anhydrase 4	CA4 Aliases: CAIV Car4	Homo sapiens (human)	Behcet's disease Zollinger-Ellison syndrome achromatopsia acquired color blindness blindness blue color blindness brain cancer cancer cataract chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm color blindness colorectal cancer colorectal carcinoma cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness corneal disease diabetes mellitus dissociated nystagmus eye disease fundus albipunctatus glaucoma hyperinsulinism hypogonadism intellectual disability keratoconus large intestine cancer learning disability lung cancer lung non-small cell carcinoma myocarditis night blindness nonpapillary renal cell carcinoma obesity obsolete asthenopia ophthalmoplegia optic atrophy papillary renal cell carcinoma pathologic nystagmus red color blindness red-green color blindness renal carcinoma renal cell carcinoma retinitis pigmentosa 17 retinitis pigmentosa sarcomatoid renal cell carcinoma sensorineural hearing loss spontaneous ocular nystagmus type 2 diabetes mellitus
392390	olfactory receptor family 1 subfamily L member 6	OR1L6	Homo sapiens (human)
256691	MAM domain containing 2	MAMDC2	Homo sapiens (human)
79004	CUE domain containing 2	CUEDC2	Homo sapiens (human)
84132	ubiquitin specific peptidase 42	USP42	Homo sapiens (human)
4677	asparaginyl-tRNA synthetase 1	NARS1	Homo sapiens (human)
1296	collagen type VIII alpha 2 chain	COL8A2	Homo sapiens (human)
284194	galectin 9B	LGALS9B	Homo sapiens (human)
968	CD68 molecule	CD68	Homo sapiens (human)
5201	prefoldin subunit 1	PFDN1	Homo sapiens (human)
9287	trace amine associated receptor 2	TAAR2	Homo sapiens (human)
126147	netrin 5	NTN5	Homo sapiens (human)
11200	checkpoint kinase 2	CHEK2	Homo sapiens (human)
57626	kelch like family member 1	KLHL1	Homo sapiens (human)
25833	POU class 2 homeobox 3	POU2F3	Homo sapiens (human)
120793	olfactory receptor family 56 subfamily A member 4	OR56A4	Homo sapiens (human)
489	ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 3	ATP2A3	Homo sapiens (human)
1521	cathepsin W	CTSW	Homo sapiens (human)
129530	lysozyme g1	LYG1 Aliases: LYGA1 SALW1939	Homo sapiens (human)	cancer
6540	solute carrier family 6 member 13	SLC6A13	Homo sapiens (human)
353174	zinc activated ion channel	ZACN	Homo sapiens (human)

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