GlyCosmos Portal

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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 **415001 - 415025** of **422592** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
23500	dishevelled associated activator of morphogenesis 2	DAAM2	Homo sapiens (human)
23499	microtubule actin crosslinking factor 1	MACF1	Homo sapiens (human)
23495	TNF receptor superfamily member 13B	TNFRSF13B	Homo sapiens (human)
23491	carboxylesterase 3	CES3	Homo sapiens (human)
23483	TDP-glucose 4,6-dehydratase	TGDS Aliases: SDR2E1 TDPGD short chain dehydrogenase/reductase family 2E, member 1	Homo sapiens (human)	Alzheimer's disease Catel Manzke syndrome Laron syndrome Marfan syndrome achondroplasia 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 cleft lip cleft palate clubfoot cryptorchidism cystic lymphangioma dementia depressive disorder dextrocardia dysthymic disorder epilepsy hydrocephalus inguinal hernia isolated cleft palate major depressive disorder melancholic depression neurotic disorder obsolete melancholia omphalocele otitis media patent foramen ovale placental insufficiency scoliosis situs inversus temtamy preaxial brachydactyly syndrome tuberous sclerosis umbilical hernia ventricular septal defect visual epilepsy
23476	bromodomain containing 4	BRD4	Homo sapiens (human)
23475	quinolinate phosphoribosyltransferase	QPRT Aliases: QPRTase nicotinate-nucleotide pyrophosphorylase (carboxylating)	Homo sapiens (human)	Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease acute myeloid leukemia adenoma adenosarcoma endemic goiter follicular adenoma gliosarcoma hepatitis C high grade glioma microcystic adenoma mixed glioma nephroblastoma neuroblastoma neurodegenerative disease papillary adenoma substernal goiter thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma
23473	calpain 7	CAPN7	Homo sapiens (human)
23471	translocation associated membrane protein 1	TRAM1	Homo sapiens (human)
23469	PHD finger protein 3	PHF3	Homo sapiens (human)
23468	chromobox 5	CBX5	Homo sapiens (human)
23467	neuronal pentraxin receptor	NPTXR	Homo sapiens (human)
23461	ATP binding cassette subfamily A member 5	ABCA5	Homo sapiens (human)
23460	ATP binding cassette subfamily A member 6	ABCA6	Homo sapiens (human)
23457	ATP binding cassette subfamily B member 9	ABCB9	Homo sapiens (human)
23456	ATP binding cassette subfamily B member 10	ABCB10	Homo sapiens (human)
23452	angiopoietin like 2	ANGPTL2	Homo sapiens (human)
23451	splicing factor 3b subunit 1	SF3B1	Homo sapiens (human)
23450	splicing factor 3b subunit 3	SF3B3	Homo sapiens (human)
23446	solute carrier family 44 member 1	SLC44A1	Homo sapiens (human)
23443	solute carrier family 35 member A3	SLC35A3 Aliases: UDP-N-acetylglucosamine transporter	Homo sapiens (human)	Marfan syndrome autism spectrum disorder autistic disorder central nervous system cancer congenital disorder of glycosylation epilepsy gliosarcoma high grade glioma intellectual disability learning disability microcephaly mixed glioma mucopolysaccharidosis IV multiple epiphyseal dysplasia osteochondrodysplasia scoliosis situs inversus spondylocostal dysostosis syndromic X-linked intellectual disability 94 tuberous sclerosis visual epilepsy
23436	chymotrypsin like elastase 3B	CELA3B	Homo sapiens (human)
23435	TAR DNA binding protein	TARDBP	Homo sapiens (human)
23432	G protein-coupled receptor 161	GPR161	Homo sapiens (human)
23430	tryptase delta 1	TPSD1	Homo sapiens (human)

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