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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 **1101 - 1125** of **393515** in total

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Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▲
266727	MAM domain containing glycosylphosphatidylinositol anchor 1	MDGA1 Aliases: GPIM MAMDC3	Homo sapiens (human)	Kawasaki disease bipolar disorder cancer depressive disorder major depressive disorder melancholic depression neurotic disorder obsolete melancholia schizophrenia
80255	solute carrier family 35 member F5	SLC35F5 Aliases: FLJ22004	Homo sapiens (human)	Kawasaki disease cancer
39596	dally-like	dlp	Drosophila melanogaster (fruit fly)	Keipert syndrome hepatocellular carcinoma omodysplasia 1
3955	LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	LFNG Aliases: SCDO3	Homo sapiens (human)	Klippel-Feil syndrome Laron syndrome Marfan syndrome achondroplasia breast cancer breast carcinoma cleft palate congenital diaphragmatic hernia cryptorchidism dysostosis hypospadias inguinal hernia intellectual disability isolated cleft palate learning disability meningocele microcephaly mucopolysaccharidosis IV multiple epiphyseal dysplasia omphalocele osteochondrodysplasia pancreatic cancer pancreatic carcinoma placental insufficiency scimitar syndrome scoliosis sickle cell anemia situs inversus spina bifida occulta spondylocostal dysostosis 3 spondylocostal dysostosis spondylolisthesis systemic primary carnitine deficiency disease tuberous sclerosis umbilical hernia
6785	ELOVL fatty acid elongase 4	ELOVL4 Aliases: CT118 cancer/testis antigen 118	Homo sapiens (human)	Kuhnt-Junius degeneration Leber congenital amaurosis Sjogren-Larsson syndrome Stargardt disease achromatopsia acquired color blindness acquired hyperkeratosis acute myocardial infarction age related macular degeneration alternating hemiplegia of childhood angioedema anhidrosis autonomic neuropathy autosomal dominant cerebellar ataxia autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis blindness blue color blindness cancer cardiac arrest central nervous system disease cerebellar ataxia cerebellar disease color blindness cone-rod dystrophy 2 cone-rod dystrophy 7 cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness corneal dystrophy coronary thrombosis degeneration of macula and posterior pole diabetes mellitus diabetic ketoacidosis dissociated nystagmus dry eye syndrome epilepsy erythrokeratodermia variabilis et progressiva 1 erythrokeratodermia variabilis eye disease fundus albipunctatus glycogen storage disease II granuloma annulare hepatocellular carcinoma hypertropia hypohidrosis ichthyosis inguinal hernia keratosis follicularis liver cancer locked-in syndrome macular degeneration mechanical strabismus mongolian spot myocardial infarction nervous system disease neurodegenerative disease night blindness obsolete congenital ichthyosiform erythroderma ophthalmoplegia pathologic nystagmus pseudoxanthoma elasticum quadriplegia red color blindness red-green color blindness retinitis pigmentosa 25 retinitis pigmentosa 30 retinitis pigmentosa silent myocardial infarction skin disease spinocerebellar ataxia type 34 spontaneous ocular nystagmus strabismus thrombocytopenia type 2 diabetes mellitus urticaria visual epilepsy xerophthalmia
22918	CD93 molecule	CD93 Aliases: C1qR(P) C1qRP CDw93 ECSM3 dJ737E23.1	Homo sapiens (human)	Kuhnt-Junius degeneration acute leukemia acute myocardial infarction allergic asthma asthma cancer central nervous system cancer chronic fatigue syndrome coronary artery disease coronary thrombosis embryoma encephalitis encephalomyelitis giant cell glioblastoma glioblastoma gliosarcoma high grade glioma intrinsic asthma lung cancer lung non-small cell carcinoma mixed glioma myelitis myocardial infarction nasopharynx carcinoma parapsoriasis psoriasis pustulosis of palm and sole silent myocardial infarction thyroid gland carcinoma vascular cancer
81579	phospholipase A2 group XIIA	PLA2G12A	Homo sapiens (human)	Kuhnt-Junius degeneration age related macular degeneration arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autism spectrum disorder autistic disorder degeneration of macula and posterior pole macular degeneration schizophrenia
2528	fucosyltransferase 6	FUT6 Aliases: FCT3A FLJ40754 FT1A FucT-VI alpha-(1,3)-fucosyltransferase galactoside 3-L-fucosyltransferase	Homo sapiens (human)	Kuhnt-Junius degeneration age related macular degeneration breast cancer cancer candidiasis carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma degeneration of macula and posterior pole embryoma hepatocellular carcinoma large intestine cancer liver cancer macular degeneration pernicious anemia prostate cancer prostate carcinoma sarcomatoid carcinoma stomach cancer stomach carcinoma
416	arylsulfatase F	ARSF Aliases: ASF	Homo sapiens (human)	Kuhnt-Junius degeneration breast cancer cancer embryoma epithelioid sarcoma hepatocellular carcinoma inflammatory bowel disease influenza liver cancer lung benign neoplasm lung cancer lung non-small cell carcinoma multiple sclerosis myositis neuroblastoma papilloma progressive multifocal leukoencephalopathy progressive muscular atrophy prostate cancer prostate carcinoma sarcoma spinal muscular atrophy spindle cell sarcoma squamous cell carcinoma squamous cell papilloma stomach cancer stomach carcinoma substance abuse substance-related disorder systemic lupus erythematosus tongue squamous cell carcinoma
79660	protein phosphatase 1 regulatory subunit 3B	PPP1R3B Aliases: FLJ14005 GL PP1 subunit R4 PPP1R4 hepatic glycogen-targeting subunit, G(L)	Homo sapiens (human)	Lafora disease alcohol use disorder antithrombin III deficiency arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis breast cancer breast carcinoma cancer coronary artery disease depressive disorder diabetes mellitus dysthymic disorder embryoma head and neck cancer major depressive disorder maturity-onset diabetes of the young melancholic depression melanoma neurotic disorder obesity obsolete melancholia post-traumatic stress disorder protein C deficiency protein S deficiency skin melanoma steatotic liver disease thrombophilia type 2 diabetes mellitus
850962	glycogen (starch) synthase GSY2	GSY2	Saccharomyces cerevisiae S288C	Lafora disease cardiovascular system disease glycogen storage disease
41823	Glycogen synthase	Glys	Drosophila melanogaster (fruit fly)	Lafora disease cardiovascular system disease glycogen storage disease
174924	Glycogen [starch] synthase	gsy-1	Caenorhabditis elegans	Lafora disease cardiovascular system disease glycogen storage disease
850569	glycogen (starch) synthase GSY1	GSY1	Saccharomyces cerevisiae S288C	Lafora disease cardiovascular system disease glycogen storage disease
690987	glycogen synthase 1	Gys1	Rattus norvegicus (Norway rat)	Lafora disease cardiovascular system disease
14936	glycogen synthase 1, muscle	Gys1	Mus musculus (house mouse)	Lafora disease cardiovascular system disease
394155	glycogen synthase 1 (muscle)	gys1	Danio rerio (zebrafish)	Lafora disease cardiovascular system disease
100490155	glycogen synthase 1	gys1	Xenopus tropicalis (tropical clawed frog)	Lafora disease cardiovascular system disease
232493	glycogen synthase 2	Gys2	Mus musculus (house mouse)	Lafora disease glycogen storage disease
373082	glycogen synthase 2	gys2	Danio rerio (zebrafish)	Lafora disease glycogen storage disease
25623	glycogen synthase 2	Gys2	Rattus norvegicus (Norway rat)	Lafora disease glycogen storage disease
13853	epilepsy, progressive myoclonic epilepsy, type 2 gene alpha	Epm2a	Mus musculus (house mouse)	Lafora disease progressive myoclonus epilepsy
114005	EPM2A glucan phosphatase, laforin	Epm2a	Rattus norvegicus (Norway rat)	Lafora disease progressive myoclonus epilepsy
105193	NHL repeat containing 1	Nhlrc1	Mus musculus (house mouse)	Lafora disease
378884	NHL repeat containing E3 ubiquitin protein ligase 1	NHLRC1	Homo sapiens (human)	Lafora disease

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