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 **351 - 375** of **422592** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
730	complement C7	C7	Homo sapiens (human)
731	complement C8 alpha chain	C8A	Homo sapiens (human)
732	complement C8 beta chain	C8B	Homo sapiens (human)
735	complement C9	C9	Homo sapiens (human)
738	VPS51 subunit of GARP complex	VPS51	Homo sapiens (human)
745	myelin regulatory factor	MYRF	Homo sapiens (human)
747	diacylglycerol lipase alpha	DAGLA Aliases: DAGLALPHA KIAA0659 NSDDR neural stem cell-derived dendrite regulator	Homo sapiens (human)
752	formin like 1	FMNL1	Homo sapiens (human)
754	PTTG1 interacting protein	PTTG1IP	Homo sapiens (human)
759	carbonic anhydrase 1	CA1	Homo sapiens (human)
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
765	carbonic anhydrase 6	CA6	Homo sapiens (human)
768	carbonic anhydrase 9	CA9	Homo sapiens (human)
770	carbonic anhydrase 11	CA11	Homo sapiens (human)
771	carbonic anhydrase 12	CA12	Homo sapiens (human)
773	calcium voltage-gated channel subunit alpha1 A	CACNA1A	Homo sapiens (human)
774	calcium voltage-gated channel subunit alpha1 B	CACNA1B	Homo sapiens (human)
775	calcium voltage-gated channel subunit alpha1 C	CACNA1C	Homo sapiens (human)
776	calcium voltage-gated channel subunit alpha1 D	CACNA1D	Homo sapiens (human)
777	calcium voltage-gated channel subunit alpha1 E	CACNA1E	Homo sapiens (human)
778	calcium voltage-gated channel subunit alpha1 F	CACNA1F	Homo sapiens (human)
779	calcium voltage-gated channel subunit alpha1 S	CACNA1S	Homo sapiens (human)
780	discoidin domain receptor tyrosine kinase 1	DDR1	Homo sapiens (human)
781	calcium voltage-gated channel auxiliary subunit alpha2delta 1	CACNA2D1 Aliases: alpha2delta-1 lncRNA-N3	Homo sapiens (human)	Brugada syndrome 1 Brugada syndrome 2 Brugada syndrome 3 Brugada syndrome 4 Brugada syndrome 5 Brugada syndrome 6 Brugada syndrome 7 Brugada syndrome 8 Brugada syndrome 9 Brugada syndrome West syndrome Williams-Beuren syndrome acute myeloid leukemia amelogenesis imperfecta type 1G atrial fibrillation atrioventricular block azoospermia brain infarction cancer cardiac arrest colon cancer colonic benign neoplasm colorectal cancer depressive disorder developmental and epileptic encephalopathy 110 embryoma epilepsy essential hypertension glaucoma hepatocellular carcinoma hypertension idiopathic scoliosis intellectual disability large intestine cancer learning disability liver cancer major depressive disorder malignant hyperthermia melancholic depression neurotic disorder obsolete infantile epileptic encephalopathy obsolete melancholia primary open angle glaucoma short QT syndrome sick sinus syndrome stomach cancer stomach carcinoma supravalvular aortic stenosis uveal melanoma
782	calcium voltage-gated channel auxiliary subunit beta 1	CACNB1	Homo sapiens (human)

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