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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 **8951 - 8975** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
201931	transmembrane protein 192	TMEM192	Homo sapiens (human)
201973	primase and DNA directed polymerase	PRIMPOL	Homo sapiens (human)
202243	coiled-coil domain containing 125	CCDC125	Homo sapiens (human)
202333	cardiomyopathy associated 5	CMYA5	Homo sapiens (human)
202559	KH RNA binding domain containing, signal transduction associated 2	KHDRBS2	Homo sapiens (human)
203068	tubulin beta class I	TUBB	Homo sapiens (human)
203074	serine protease 55	PRSS55	Homo sapiens (human)
203102	ADAM metallopeptidase domain 32	ADAM32	Homo sapiens (human)
203190	leucine rich repeat LGI family member 3	LGI3	Homo sapiens (human)
203228	C9orf72-SMCR8 complex subunit	C9orf72	Homo sapiens (human)
203328	sushi domain containing 3	SUSD3	Homo sapiens (human)
203413	cancer/testis antigen 83	CT83	Homo sapiens (human)
203447	Nik related kinase	NRK	Homo sapiens (human)
203523	zinc finger protein 449	ZNF449	Homo sapiens (human)
203859	anoctamin 5	ANO5	Homo sapiens (human)
204219	ceramide synthase 3	CERS3 Aliases: MGC27091	Homo sapiens (human)	Laron syndrome Sjogren-Larsson syndrome Weill-Marchesani syndrome achondroplasia acrodermatitis alopecia anhidrosis atopic dermatitis autosomal recessive congenital ichthyosis 10 autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis 2 autosomal recessive congenital ichthyosis 3 autosomal recessive congenital ichthyosis 4A autosomal recessive congenital ichthyosis 5 autosomal recessive congenital ichthyosis 6 autosomal recessive congenital ichthyosis 7 autosomal recessive congenital ichthyosis 8 autosomal recessive congenital ichthyosis 9 autosomal recessive congenital ichthyosis dermatitis ectropion hypohidrosis ichthyosis keratitis keratoconjunctivitis keratosis follicularis mongolian spot nonepidermolytic palmoplantar keratoderma obsolete congenital ichthyosiform erythroderma palmoplantar keratosis pseudoxanthoma elasticum sensorineural hearing loss
204474	protein disulfide isomerase like, testis expressed	PDILT	Homo sapiens (human)
204801	NLR family pyrin domain containing 11	NLRP11	Homo sapiens (human)
204851	homeodomain interacting protein kinase 1	HIPK1	Homo sapiens (human)
204962	solute carrier family 44 member 5	SLC44A5	Homo sapiens (human)
205147	APC membrane recruitment protein 3	AMER3	Homo sapiens (human)
205428	divergent protein kinase domain 2A	DIPK2A	Homo sapiens (human)
205564	SUMO specific peptidase 5	SENP5	Homo sapiens (human)
205717	upstream transcription factor family member 3	USF3	Homo sapiens (human)
206338	laeverin	LVRN	Homo sapiens (human)

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