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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 **7326 - 7350** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
79731	asparaginyl-tRNA synthetase 2, mitochondrial	NARS2	Homo sapiens (human)
79733	E2F transcription factor 8	E2F8	Homo sapiens (human)
79736	transcription elongation factor, mitochondrial	TEFM	Homo sapiens (human)
79741	coiled-coil domain containing 7	CCDC7	Homo sapiens (human)
79742	divergent protein kinase domain 2B	DIPK2B	Homo sapiens (human)
79745	CAP-Gly domain containing linker protein family member 4	CLIP4	Homo sapiens (human)
79748	lectin, mannose binding 1 like	LMAN1L Aliases: ERGIC-53L ERGL	Homo sapiens (human)
79750	zinc finger protein 385D	ZNF385D	Homo sapiens (human)
79755	zinc finger protein 750	ZNF750	Homo sapiens (human)
79767	engulfment and cell motility 3	ELMO3	Homo sapiens (human)
79770	thioredoxin domain containing 15	TXNDC15	Homo sapiens (human)
79776	zinc finger homeobox 4	ZFHX4	Homo sapiens (human)
79778	MICAL like 2	MICALL2	Homo sapiens (human)
79781	IQ motif containing with AAA domain 1	IQCA1	Homo sapiens (human)
79784	myosin heavy chain 14	MYH14	Homo sapiens (human)
79789	calmin	CLMN	Homo sapiens (human)
79791	F-box protein 31	FBXO31	Homo sapiens (human)
79792	gasdermin D	GSDMD	Homo sapiens (human)
79794	SREBF pathway regulator in golgi 1	SPRING1	Homo sapiens (human)
79796	ALG9 alpha-1,2-mannosyltransferase	ALG9 Aliases: dol-P-Man dependent alpha-1,2-mannosyltransferase dolichyl-P-Man:Man(6)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase dolichyl-P-Man:Man(8)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase	Homo sapiens (human)	Gilles de la Tourette syndrome Marfan syndrome Meckel syndrome 1 Meckel syndrome 2 Meckel syndrome 3 Meckel syndrome 4 Meckel syndrome 5 Meckel syndrome 6 Meckel syndrome 8 Meckel syndrome autosomal dominant polycystic kidney disease cardiovascular system disease congenital disorder of glycosylation Il congenital disorder of glycosylation type I congenital disorder of glycosylation congenital heart disease congestive heart failure craniosynostosis cystic kidney disease cystinuria enophthalmos epilepsy esotropia galactokinase deficiency galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease heart disease heart septal defect hemopericardium intellectual disability learning disability microcephaly monocular esotropia mucopolysaccharidosis IV multiple epiphyseal dysplasia neuroendocrine carcinoma neuroendocrine tumor obsolete exophthalmos orbital disease osteochondrodysplasia pericardial effusion polycystic kidney disease 1 polycystic liver disease psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder situs inversus tuberous sclerosis visual epilepsy
79799	UDP glucuronosyltransferase family 2 member A3	UGT2A3 Aliases: FLJ21934	Homo sapiens (human)
79802	HHIP like 2	HHIPL2	Homo sapiens (human)
79805	vasohibin 2	VASH2	Homo sapiens (human)
79811	SAFB like transcription modulator	SLTM	Homo sapiens (human)
79812	multimerin 2	MMRN2	Homo sapiens (human)

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