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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 **8751 - 8775** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
154141	membrane bound O-acyltransferase domain containing 1	MBOAT1 Aliases: LPEAT1 LPLAT14 MGC44669 dJ434O11.1 lysophosphatidylethanolamine acyltransferase 1 lysophospholipid acyltransferase 1 lysophospholipid acyltransferase 14	Homo sapiens (human)	brachydactyly-syndactyly syndrome cholestasis
154197	PARN like ribonuclease domain containing exonuclease 1	PNLDC1	Homo sapiens (human)
154313	cilia and flagella associated protein 206	CFAP206	Homo sapiens (human)
154664	ATP binding cassette subfamily A member 13	ABCA13	Homo sapiens (human)
154790	C-type lectin domain family 2 member L	CLEC2L Aliases: FLJ32986	Homo sapiens (human)
154796	angiomotin	AMOT	Homo sapiens (human)
155066	ATPase H+ transporting V0 subunit e2	ATP6V0E2	Homo sapiens (human)
155184	solute carrier family 2 member 7	SLC2A7	Homo sapiens (human)
155435	RNA binding motif protein 33	RBM33	Homo sapiens (human)
155465	anterior gradient 3, protein disulphide isomerase family member	AGR3	Homo sapiens (human)
157310	phosphatidylethanolamine binding protein 4	PEBP4	Homo sapiens (human)
157313	cell division cycle associated 2	CDCA2	Homo sapiens (human)
157570	establishment of sister chromatid cohesion N-acetyltransferase 2	ESCO2	Homo sapiens (human)
157680	vacuolar protein sorting 13 homolog B	VPS13B	Homo sapiens (human)
157773	chromosome 8 open reading frame 48	C8orf48	Homo sapiens (human)
157855	potassium calcium-activated channel subfamily U member 1	KCNU1	Homo sapiens (human)
157869	somatomedin B and thrombospondin type 1 domain containing	SBSPON	Homo sapiens (human)
157922	calmodulin regulated spectrin associated protein 1	CAMSAP1	Homo sapiens (human)
158038	leucine rich repeat and Ig domain containing 2	LINGO2	Homo sapiens (human)
158056	MAM domain containing 4	MAMDC4	Homo sapiens (human)
158131	olfactory receptor family 1 subfamily Q member 1	OR1Q1	Homo sapiens (human)
158234	tRNA methyltransferase 10B	TRMT10B	Homo sapiens (human)
158326	FRAS1 related extracellular matrix 1	FREM1 Aliases: C9orf143 C9orf145 DKFZp686M16108 FLJ25461 TILRR	Homo sapiens (human)	3p deletion syndrome Angelman syndrome Baraitser-Winter syndrome CAKUT Fraser syndrome 1 Fraser syndrome Goldenhar syndrome Moebius syndrome Muenke Syndrome NFIA-related disorder Nance-Horan syndrome Potter's syndrome SATB2-associated syndrome Sakati-Nyhan syndrome Smith-Magenis syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome acquired immunodeficiency syndrome anorectal stricture bilateral renal aplasia branchiootic syndrome cardiovascular system disease chromosome 13q14 deletion syndrome chromosome 15q13.3 microdeletion syndrome chromosome 15q24 deletion syndrome chromosome 15q26-qter deletion syndrome chromosome 16p11.2 deletion syndrome, 220-kb chromosome 16p12.2-p11.2 deletion syndrome chromosome 17q12 deletion syndrome chromosome 17q23.1-q23.2 deletion syndrome chromosome 18q deletion syndrome chromosome 1q21.1 deletion syndrome chromosome 1q41-q42 deletion syndrome chromosome 2p16.1-p15 deletion syndrome chromosome 6pter-p24 deletion syndrome chromosome 8q21.11 deletion syndrome chromosome 9p deletion syndrome congenital diaphragmatic hernia craniosynostosis distal 10q deletion syndrome eye disease heart disease hiatus hernia human immunodeficiency virus infectious disease microphthalmia myelofibrosis omphalocele orofaciodigital syndrome I orofaciodigital syndrome X rectal prolapse renal agenesis umbilical hernia
158358	bromodomain containing 10	BRD10	Homo sapiens (human)
158399	zinc finger protein 483	ZNF483	Homo sapiens (human)

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