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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 **7776 - 7800** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
84632	actin filament associated protein 1 like 2	AFAP1L2	Homo sapiens (human)
84634	KISS1 receptor	KISS1R	Homo sapiens (human)
84636	G protein-coupled receptor 174	GPR174	Homo sapiens (human)
84640	ubiquitin specific peptidase 38	USP38	Homo sapiens (human)
84641	major facilitator superfamily domain containing 14B	MFSD14B	Homo sapiens (human)
84647	phospholipase A2 group XIIB	PLA2G12B	Homo sapiens (human)	membranous glomerulonephritis
84649	diacylglycerol O-acyltransferase 2	DGAT2	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 agenesis of the corpus callosum with peripheral neuropathy androgen insensitivity syndrome cancer cholestasis chronic kidney disease generalized atherosclerosis hepatitis B hepatitis C hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 liver cancer metabolic dysfunction-associated steatotic liver disease motor peripheral neuropathy neuropathy obesity obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum peripheral nervous system disease polyneuropathy premature menopause prostate cancer prostate carcinoma steatotic liver disease
84654	spermatogenic leucine zipper 1	SPZ1	Homo sapiens (human)
84658	adhesion G protein-coupled receptor E3	ADGRE3	Homo sapiens (human)
84659	ribonuclease A family member 7	RNASE7	Homo sapiens (human)
84660	coiled-coil domain containing 62	CCDC62	Homo sapiens (human)
84665	myopalladin	MYPN	Homo sapiens (human)
84668	hyccin PI4KA lipid kinase complex subunit 1	HYCC1	Homo sapiens (human)
84674	caspase recruitment domain family member 6	CARD6	Homo sapiens (human)
84675	tripartite motif containing 55	TRIM55	Homo sapiens (human)
84676	tripartite motif containing 63	TRIM63	Homo sapiens (human)
84678	lysine demethylase 2B	KDM2B	Homo sapiens (human)
84679	solute carrier family 9 member A7	SLC9A7	Homo sapiens (human)
84687	protein phosphatase 1 regulatory subunit 9B	PPP1R9B	Homo sapiens (human)
84693	methylmalonyl-CoA epimerase	MCEE Aliases: GLOD2 MCE MMCE glyoxalase domain containing 2 methylmalonyl CoA isomerase	Homo sapiens (human)	disease of metabolism esophagitis gastroesophageal reflux disease lactic acidosis methylmalonic acidemia peptic esophagitis pneumonia sepiapterin reductase deficiency
84695	lysyl oxidase like 3	LOXL3	Homo sapiens (human)
84696	abhydrolase domain containing 1	ABHD1	Homo sapiens (human)
84699	cAMP responsive element binding protein 3 like 3	CREB3L3	Homo sapiens (human)
84700	myosin XVIIIB	MYO18B	Homo sapiens (human)
84701	cytochrome c oxidase subunit 4I2	COX4I2	Homo sapiens (human)

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