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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 **9926 - 9950** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
1286	collagen type IV alpha 4 chain	COL4A4	Homo sapiens (human)
85413	solute carrier family 22 member 16	SLC22A16	Homo sapiens (human)
11126	CD160 molecule	CD160	Homo sapiens (human)
27433	torsin family 2 member A	TOR2A	Homo sapiens (human)
10486	cyclase associated actin cytoskeleton regulatory protein 2	CAP2	Homo sapiens (human)
4210	MEFV innate immunity regulator, pyrin	MEFV	Homo sapiens (human)
84569	lysozyme like 1	LYZL1 Aliases: LYC2 MGC33408	Homo sapiens (human)
11342	ring finger protein 13	RNF13	Homo sapiens (human)
54922	Ras interacting protein 1	RASIP1	Homo sapiens (human)
3684	integrin subunit alpha M	ITGAM	Homo sapiens (human)
9517	serine palmitoyltransferase long chain base subunit 2	SPTLC2 Aliases: KIAA0526 LCB2 LCB2A hLCB2a	Homo sapiens (human)	Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease acute myocardial infarction agenesis of the corpus callosum with peripheral neuropathy anhidrosis cancer coronary thrombosis diarrhea hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 1 hereditary sensory and autonomic neuropathy type 1A hereditary sensory and autonomic neuropathy type 1C hereditary sensory and autonomic neuropathy type 2 hereditary sensory neuropathy hypohidrosis liver cancer motor peripheral neuropathy myocardial infarction neuropathy obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum osteomyelitis parapsoriasis peripheral nervous system disease psoriasis pustulosis of palm and sole sensory peripheral neuropathy silent myocardial infarction teratocarcinoma
57611	immunoglobulin superfamily containing leucine rich repeat 2	ISLR2	Homo sapiens (human)
219959	olfactory receptor family 1 subfamily S member 1	OR1S1	Homo sapiens (human)
26032	sushi domain containing 5	SUSD5	Homo sapiens (human)
54020	solute carrier family 37 member 1	SLC37A1	Homo sapiens (human)
25806	ventral anterior homeobox 2	VAX2	Homo sapiens (human)
57519	StAR related lipid transfer domain containing 9	STARD9	Homo sapiens (human)
27120	dickkopf like acrosomal protein 1	DKKL1	Homo sapiens (human)
93953	germ cell nuclear acidic peptidase	GCNA	Homo sapiens (human)
6533	solute carrier family 6 member 6	SLC6A6	Homo sapiens (human)
4282	macrophage migration inhibitory factor	MIF	Homo sapiens (human)
2263	fibroblast growth factor receptor 2	FGFR2	Homo sapiens (human)
96459	folliculin interacting protein 1	FNIP1	Homo sapiens (human)
1672	defensin beta 1	DEFB1	Homo sapiens (human)
51365	phospholipase A1 member A	PLA1A Aliases: phosphatidylserine-specific phospholipase A1 ps-PLA1	Homo sapiens (human)

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