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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	July 8, 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 **391226 - 391250** of **393515** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
115290	F-box protein 17	FBXO17 Aliases: F-box only protein 26 FBG4 FLJ11798 FLJ25205 Fbx17 MGC9379	Homo sapiens (human)	cancer embryoma gliosarcoma hepatocellular carcinoma high grade glioma liver cancer lung cancer lung non-small cell carcinoma mixed glioma
115209	OMA1 zinc metallopeptidase	OMA1	Homo sapiens (human)
114805	polypeptide N-acetylgalactosaminyltransferase 13	GALNT13 Aliases: GalNAc-T13 KIAA1918 UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 13 polypeptide GalNAc transferase 13	Homo sapiens (human)	cancer chronic obstructive pulmonary disease lung benign neoplasm lung carcinoma sickle cell anemia
114780	polycystin 1 like 2 (gene/pseudogene)	PKD1L2 Aliases: KIAA1879	Homo sapiens (human)	Meckel syndrome autosomal dominant polycystic kidney disease colorectal cancer colorectal carcinoma familial periodic paralysis hypoplastic left heart syndrome large intestine cancer myopathy neuromuscular disease
114711	glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase	Gne	Rattus norvegicus (Norway rat)	GNE myopathy sialuria
114515	LanC like glutathione S-transferase 1	Lancl1	Rattus norvegicus (Norway rat)
114508	fructose-bisphosphatase 2	Fbp2	Rattus norvegicus (Norway rat)
114132	sialic acid binding Ig like lectin 11	SIGLEC11	Homo sapiens (human)
114104	N-acylsphingosine amidohydrolase 2	Asah2	Rattus norvegicus (Norway rat)	cardiomyopathy
114005	EPM2A glucan phosphatase, laforin	Epm2a	Rattus norvegicus (Norway rat)	Lafora disease progressive myoclonus epilepsy
114002	N-deacetylase and N-sulfotransferase 2	Ndst2	Rattus norvegicus (Norway rat)	autism spectrum disorder azoospermia intellectual disability
113992	UDP glucuronosyltransferase family 1 member A6	Ugt1a6	Rattus norvegicus (Norway rat)	hepatitis B type 2 diabetes mellitus
113901	chitinase, acidic	Chia	Rattus norvegicus (Norway rat)	asthma cryptococcosis silicosis sinusitis
113829	solute carrier family 35 member A4	SLC35A4	Homo sapiens (human)	breast cancer cancer hepatocellular carcinoma liver cancer lung adenocarcinoma lung cancer multiple myeloma
113622	ADP-ribosylhydrolase like 1	ADPRHL1	Homo sapiens (human)
113612	cytochrome P450 family 2 subfamily U member 1	CYP2U1 Aliases: SPG49 spastic paraplegia 49	Homo sapiens (human)	Charcot-Marie-Tooth disease type 5 GM1 gangliosidosis type 1 GM1 gangliosidosis Henoch-Schoenlein purpura MASA syndrome Mast syndrome SPOAN syndrome Troyer syndrome agnosia blindness breast cancer breast carcinoma cancer developmental coordination disorder dystonia embryoma focal hand dystonia generalized dystonia hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia hypersensitivity vasculitis intellectual disability learning disability neurodegenerative disease neuropathy paraplegia peripheral nervous system disease polyneuropathy syringomyelia
113189	carbohydrate sulfotransferase 14	CHST14 Aliases: D4ST-1 HD4ST	Homo sapiens (human)	Ehlers-Danlos syndrome musculocontractural type 1 Ehlers-Danlos syndrome Marfan syndrome Peters anomaly agnosia arthropathy atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect brittle cornea syndrome 1 cleft palate clubfoot congenital diaphragmatic hernia cornea plana craniosynostosis cryptorchidism developmental coordination disorder distal arthrogryposis familial nephrotic syndrome familial periodic paralysis glaucoma hiatus hernia hydrocephalus hydronephrosis hypertropia isolated cleft palate lipoid nephrosis mechanical strabismus myopathy myopia nephrotic syndrome obsolete constipation omphalocele ophthalmoplegia osteogenesis imperfecta patent foramen ovale pneumothorax prostate cancer prostate carcinoma retinal detachment scoliosis sensorineural hearing loss situs inversus strabismus tuberous sclerosis umbilical hernia
113026	phospholipase C delta 3	PLCD3	Homo sapiens (human)	Goldenhar syndrome acquired immunodeficiency syndrome alcohol dependence alcohol use disorder arteriosclerotic cardiovascular disease atherosclerosis coronary artery disease human immunodeficiency virus infectious disease microphthalmia nasopharynx carcinoma obsolete Matthew-Wood syndrome senile cataract
112937	galactosidase beta 1 like 3	GLB1L3 Aliases: FLJ90231	Homo sapiens (human)
112817	4-hydroxy-2-oxoglutarate aldolase 1	HOGA1 Aliases: DHDPS2 FLJ37472 N-acetylneuraminate pyruvate lyase 2 (putative) NPL2 dihydrodipicolinate synthetase homolog 2 (E. coli)	Homo sapiens (human)	calcinosis calcium metabolism disease cholestasis chronic kidney disease hypercalcemia nephrocalcinosis nephrolithiasis phosphorus metabolism disease primary hyperoxaluria type 3 primary hyperoxaluria
112417	UDP glucuronosyltransferase 2 family, polypeptide B37	Ugt2b37	Mus musculus (house mouse)
110208	phosphogluconate dehydrogenase	Pgd	Mus musculus (house mouse)
110173	mannosidase, beta A, lysosomal	Manba	Mus musculus (house mouse)	beta-mannosidosis
110119	mannose phosphate isomerase	Mpi	Mus musculus (house mouse)	carbohydrate metabolic disorder congenital disorder of glycosylation Ib congenital disorder of glycosylation type I
110095	liver glycogen phosphorylase	Pygl	Mus musculus (house mouse)	glycogen storage disease VI glycogen storage disease lactic acidosis

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