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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 **8101 - 8125** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
112942	cilia and flagella associated protein 36	CFAP36	Homo sapiens (human)
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
113130	cell division cycle associated 5	CDCA5	Homo sapiens (human)
113146	AHNAK nucleoprotein 2	AHNAK2	Homo sapiens (human)
113177	IZUMO family member 4	IZUMO4	Homo sapiens (human)
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
113201	golgi membrane protein 2	GOLM2	Homo sapiens (human)
113230	MISP family member 3	MISP3	Homo sapiens (human)
113235	solute carrier family 46 member 1	SLC46A1	Homo sapiens (human)
113251	La ribonucleoprotein 4	LARP4	Homo sapiens (human)
113263	glucocorticoid induced 1	GLCCI1	Homo sapiens (human)
113278	solute carrier family 52 member 3	SLC52A3	Homo sapiens (human)
113510	helicase, POLQ like	HELQ	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
113622	ADP-ribosylhydrolase like 1	ADPRHL1	Homo sapiens (human)
113730	kelch domain containing 7B	KLHDC7B	Homo sapiens (human)
113791	phosphoinositide-3-kinase interacting protein 1	PIK3IP1	Homo sapiens (human)
113829	solute carrier family 35 member A4	SLC35A4	Homo sapiens (human)	breast cancer cancer hepatocellular carcinoma liver cancer lung adenocarcinoma lung cancer multiple myeloma
113878	deltex E3 ubiquitin ligase 2	DTX2	Homo sapiens (human)
114034	target of EGR1, exonuclease	TOE1	Homo sapiens (human)
114049	BUD23 rRNA methyltransferase and ribosome maturation factor	BUD23	Homo sapiens (human)
114132	sialic acid binding Ig like lectin 11	SIGLEC11	Homo sapiens (human)
114134	solute carrier family 2 member 13	SLC2A13	Homo sapiens (human)
114294	lactamase beta	LACTB	Homo sapiens (human)
114335	chorionic gonadotropin subunit beta 1	CGB1	Homo sapiens (human)

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