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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 **8001 - 8025** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
23513	scribble planar cell polarity protein	SCRIB	Homo sapiens (human)
81831	neuropilin and tolloid like 2	NETO2	Homo sapiens (human)
7222	transient receptor potential cation channel subfamily C member 3	TRPC3	Homo sapiens (human)
5634	phosphoribosyl pyrophosphate synthetase 2	PRPS2 Aliases: PRS II ribose-phosphate diphosphokinase 2	Homo sapiens (human)	Sertoli cell-only syndrome X-linked spermatogenic failure 1 Y-linked spermatogenic failure 1 cancer embryoma oligospermia systemic lupus erythematosus
6781	stanniocalcin 1	STC1	Homo sapiens (human)
9180	oncostatin M receptor	OSMR	Homo sapiens (human)
1855	dishevelled segment polarity protein 1	DVL1	Homo sapiens (human)
11255	histamine receptor H3	HRH3	Homo sapiens (human)
128312	H2B clustered histone 26	H2BC26	Homo sapiens (human)
57864	solute carrier family 46 member 2	SLC46A2	Homo sapiens (human)
220082	chibby family member 2	CBY2	Homo sapiens (human)
85463	zinc finger CCCH-type containing 12C	ZC3H12C	Homo sapiens (human)
58158	neuronal differentiation 4	NEUROD4	Homo sapiens (human)
79053	ALG8 alpha-1,3-glucosyltransferase	ALG8 Aliases: MGC2840 dolichyl-P-Glc:Glc(1)Man(9)GlcNAc(2)-PP-dolichol alpha- 1->3-glucosyltransferase	Homo sapiens (human)	Meckel syndrome 1 Meckel syndrome 2 Meckel syndrome 3 Meckel syndrome 4 Meckel syndrome 5 Meckel syndrome 6 Meckel syndrome 8 anemia asphyxia neonatorum autosomal dominant polycystic kidney disease cataract cholestasis clubfoot congenital disorder of glycosylation Ih congenital disorder of glycosylation type I congenital disorder of glycosylation congenital hypothyroidism cryptorchidism cystic kidney disease depressive disorder developmental and epileptic encephalopathy 36 diarrhea dysthymic disorder elephantiasis gastrointestinal system disease heart septal defect hypothyroidism intestinal disease lymphedema macrocytic anemia major depressive disorder melancholic depression myxedema neurotic disorder non-congenital cyst of kidney obsolete melancholia oligohydramnios patent ductus arteriosus placental insufficiency polycystic liver disease polyhydramnios protein-losing enteropathy thrombocytopenia
965	CD58 molecule	CD58	Homo sapiens (human)
10618	trans-golgi network protein 2	TGOLN2	Homo sapiens (human)
341880	solute carrier family 35 member F4	SLC35F4 Aliases: FLJ37712	Homo sapiens (human)	acquired immunodeficiency syndrome bipolar disorder
1600	DAB adaptor protein 1	DAB1	Homo sapiens (human)
286204	crumbs cell polarity complex component 2	CRB2	Homo sapiens (human)
4224	meprin A subunit alpha	MEP1A	Homo sapiens (human)
9520	aminopeptidase puromycin sensitive	NPEPPS	Homo sapiens (human)
1620	BMP/retinoic acid inducible neural specific 1	BRINP1	Homo sapiens (human)
4883	natriuretic peptide receptor 3	NPR3	Homo sapiens (human)
401612	solute carrier family 25 member 53	SLC25A53	Homo sapiens (human)
23211	zinc finger CCCH-type containing 4	ZC3H4	Homo sapiens (human)

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