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 **401 - 425** of **423164** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
829	capping actin protein of muscle Z-line subunit alpha 1	CAPZA1	Homo sapiens (human)
831	calpastatin	CAST	Homo sapiens (human)	PLACK syndrome Parkinson's disease Sjogren's syndrome congenital myasthenic syndrome 1A pemphigus psoriasis rheumatoid arthritis systemic lupus erythematosus vasculitis
832	capping actin protein of muscle Z-line subunit beta	CAPZB	Homo sapiens (human)
833	cysteinyl-tRNA synthetase 1	CARS1	Homo sapiens (human)
839	caspase 6	CASP6	Homo sapiens (human)	ovarian carcinoma
840	caspase 7	CASP7	Homo sapiens (human)	Alzheimer's disease breast cancer colon cancer lung non-small cell carcinoma
842	caspase 9	CASP9	Homo sapiens (human)	Parkinson's disease colorectal cancer lung non-small cell carcinoma pancreatic cancer type 2 diabetes mellitus urinary bladder cancer
844	calsequestrin 1	CASQ1	Homo sapiens (human)	type 2 diabetes mellitus
845	calsequestrin 2	CASQ2	Homo sapiens (human)	catecholaminergic polymorphic ventricular tachycardia 2
846	calcium sensing receptor	CASR	Homo sapiens (human)	autosomal dominant hypocalcemia 1 autosomal dominant hypocalcemia calcium oxalate nephrolithiasis familial hypocalciuric hypercalcemia 1 hypercalcemia hyperparathyroidism intellectual disability nephrolithiasis obsolete idiopathic generalized epilepsy 8 secondary hyperparathyroidism
847	catalase	CAT	Homo sapiens (human)	acatalasia angle-closure glaucoma asthma essential hypertension hepatocellular carcinoma keratosis lung disease melanoma newborn respiratory distress syndrome optic neuritis osteonecrosis pseudoxanthoma elasticum retinitis pigmentosa senile cataract vitiligo
860	RUNX family transcription factor 2	RUNX2	Homo sapiens (human)	cleidocranial dysplasia lung non-small cell carcinoma metaphyseal dysplasia-maxillary hypoplasia-brachydactyly syndrome
861	RUNX family transcription factor 1	RUNX1	Homo sapiens (human)	acute myeloid leukemia esophagus squamous cell carcinoma
862	RUNX1 partner transcriptional co-repressor 1	RUNX1T1	Homo sapiens (human)
864	RUNX family transcription factor 3	RUNX3	Homo sapiens (human)	breast cancer developmental disorder of mental health endometrial carcinoma in situ carcinoma invasive ductal carcinoma lung non-small cell carcinoma ovarian cancer pancreatic cancer urinary bladder cancer
865	core-binding factor subunit beta	CBFB	Homo sapiens (human)	acute myelomonocytic leukemia
866	serpin family A member 6	SERPINA6	Homo sapiens (human)	corticosteroid-binding globulin deficiency
867	Cbl proto-oncogene	CBL	Homo sapiens (human)	acute myeloid leukemia congestive heart failure juvenile myelomonocytic leukemia lung non-small cell carcinoma myeloid neoplasm
869	cerebellin 1 precursor	CBLN1	Homo sapiens (human)
871	serpin family H member 1	SERPINH1	Homo sapiens (human)	osteogenesis imperfecta type 10 preterm premature rupture of the membranes
873	carbonyl reductase 1	CBR1 Aliases: SDR21C1 short chain dehydrogenase/reductase family 21C, member 1	Homo sapiens (human)
874	carbonyl reductase 3	CBR3 Aliases: SDR21C2 short chain dehydrogenase/reductase family 21C, member 2	Homo sapiens (human)
875	cystathionine beta-synthase	CBS	Homo sapiens (human)	cerebral infarction coronary artery disease homocystinuria hyperhomocysteinemia malaria neural tube defect
885	cholecystokinin	CCK	Homo sapiens (human)	alcohol dependence nicotine dependence
886	cholecystokinin A receptor	CCKAR	Homo sapiens (human)	obesity

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