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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 **8201 - 8225** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▼	Disease Ontology
2596	growth associated protein 43	GAP43	Homo sapiens (human)
23013	spen family transcriptional repressor	SPEN	Homo sapiens (human)
23163	golgi associated, gamma adaptin ear containing, ARF binding protein 3	GGA3	Homo sapiens (human)
7840	ALMS1 centrosome and basal body associated protein	ALMS1	Homo sapiens (human)
537	ATPase H+ transporting accessory protein 1	ATP6AP1 Aliases: 16A Ac45 CF2 ORF VATPS1 X-associated protein 3 XAP-3 XAP3 vacuolar ATPase subunit S1	Homo sapiens (human)	Hailey-Hailey disease Rothmund-Thomson syndrome autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB cancer congenital disorder of glycosylation cutis laxa exocrine pancreatic insufficiency follicular lymphoma gallbladder disease hyperopia immunodeficiency 47 leukopenia liver disease mal de Meleda restrictive dermopathy steatotic liver disease tuberculosis
347	apolipoprotein D	APOD	Homo sapiens (human)	Alzheimer's disease gestational diabetes obesity status epilepticus type 2 diabetes mellitus vasculogenic impotence
152	adrenoceptor alpha 2C	ADRA2C	Homo sapiens (human)
60506	nyctalopin	NYX Aliases: CLRP CSNB1A	Homo sapiens (human)	Balo concentric sclerosis Leber congenital amaurosis 1 Stargardt disease achromatopsia 3 achromatopsia acquired color blindness adrenoleukodystrophy blue color blindness central nervous system disease color blindness cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness 1B congenital stationary night blindness 2A congenital stationary night blindness dissociated nystagmus enhanced S-cone syndrome eye disease fundus albipunctatus hypertropia leukemia mechanical strabismus myopia narcolepsy nervous system disease night blindness ophthalmoplegia pathologic nystagmus red color blindness red-green color blindness retinal disease retinitis pigmentosa retinitis spontaneous ocular nystagmus strabismus
114990	vasorin	VASN	Homo sapiens (human)
79152	fatty acid 2-hydroxylase	FA2H	Homo sapiens (human)
5604	mitogen-activated protein kinase kinase 1	MAP2K1	Homo sapiens (human)
158724	family with sequence similarity 47 member A	FAM47A	Homo sapiens (human)
915	CD3 delta subunit of T-cell receptor complex	CD3D	Homo sapiens (human)
3676	integrin subunit alpha 4	ITGA4	Homo sapiens (human)
64090	galactose-3-O-sulfotransferase 2	GAL3ST2 Aliases: GP3ST	Homo sapiens (human)	Crohn's colitis Crohn's disease ankylosing spondylitis ascending cholangitis cholangitis inflammatory bowel disease 1 inflammatory bowel disease parapsoriasis primary sclerosing cholangitis prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole sclerosing cholangitis suppurative cholangitis ulcerative colitis
399474	transmembrane protein 200B	TMEM200B	Homo sapiens (human)
147710	immunoglobulin superfamily member 23	IGSF23	Homo sapiens (human)
219952	olfactory receptor family 6 subfamily Q member 1	OR6Q1	Homo sapiens (human)
140679	solute carrier family 32 member 1	SLC32A1	Homo sapiens (human)
50618	intersectin 2	ITSN2	Homo sapiens (human)
8270	L antigen family member 3	LAGE3	Homo sapiens (human)
1111	checkpoint kinase 1	CHEK1	Homo sapiens (human)
64711	heparan sulfate-glucosamine 3-sulfotransferase 6	HS3ST6	Homo sapiens (human)	anthracosilicosis asbestosis bagassosis hereditary angioedema herpes simplex pneumoconiosis siderosis
10092	actin related protein 2/3 complex subunit 5	ARPC5	Homo sapiens (human)
26762	hepatitis A virus cellular receptor 1	HAVCR1	Homo sapiens (human)

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