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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 **6976 - 7000** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▼	Organism	Disease Ontology
391059	ferric chelate reductase 1	FRRS1	Homo sapiens (human)
9758	FERM and PDZ domain containing 4	FRMPD4	Homo sapiens (human)
23150	FERM domain containing 4B	FRMD4B	Homo sapiens (human)
166752	FRAS1 related extracellular matrix 3	FREM3	Homo sapiens (human)
341640	FRAS1 related extracellular matrix 2	FREM2	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
80144	Fraser extracellular matrix complex subunit 1	FRAS1	Homo sapiens (human)
2359	formyl peptide receptor 3	FPR3	Homo sapiens (human)
2358	formyl peptide receptor 2	FPR2	Homo sapiens (human)
2357	formyl peptide receptor 1	FPR1	Homo sapiens (human)
8790	fucose-1-phosphate guanylyltransferase	FPGT Aliases: GFPP	Homo sapiens (human)	chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma
80020	FAD dependent oxidoreductase domain containing 2	FOXRED2	Homo sapiens (human)
116113	forkhead box P4	FOXP4	Homo sapiens (human)
93986	forkhead box P2	FOXP2	Homo sapiens (human)
27086	forkhead box P1	FOXP1	Homo sapiens (human)
4303	forkhead box O4	FOXO4	Homo sapiens (human)
2309	forkhead box O3	FOXO3	Homo sapiens (human)
2308	forkhead box O1	FOXO1	Homo sapiens (human)
1112	forkhead box N3	FOXN3	Homo sapiens (human)
2305	forkhead box M1	FOXM1	Homo sapiens (human)
401089	FOXL2 neighbor	FOXL2NB	Homo sapiens (human)
668	forkhead box L2	FOXL2	Homo sapiens (human)
3607	forkhead box K2	FOXK2	Homo sapiens (human)
221937	forkhead box K1	FOXK1	Homo sapiens (human)
55810	forkhead box J2	FOXJ2	Homo sapiens (human)

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