GlyCosmos Portal

Table Filtering

Gene ID

Gene Name

Gene Symbol

Organism

Taxonomy ID

Disease Ontology

Disease Ontology ID

Gene Ontology

Gene Ontology ID

Display
results per page.

Clear

Submissions

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 **414126 - 414150** of **422592** in total

« First

‹ Prev

…

16562

16563

16564

16565

16566

16567

16568

16569

16570

…

Next ›

Last »
Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
26561	matrix metallopeptidase 23	Mmp23	Mus musculus (house mouse)
26556	homer scaffolding protein 1	Homer1	Mus musculus (house mouse)
26554	cullin 3	Cul3	Mus musculus (house mouse)
26539	olfactory receptor family 10 subfamily H member 1	OR10H1	Homo sapiens (human)
26538	olfactory receptor family 10 subfamily H member 2	OR10H2	Homo sapiens (human)
26534	olfactory receptor family 10 subfamily G member 2	OR10G2	Homo sapiens (human)
26533	olfactory receptor family 10 subfamily G member 3	OR10G3	Homo sapiens (human)
26531	olfactory receptor family 11 subfamily A member 1	OR11A1	Homo sapiens (human)
26530	olfactory receptor family 12 subfamily D member 1 (gene/pseudogene)	OR12D1	Homo sapiens (human)
26529	olfactory receptor family 12 subfamily D member 2	OR12D2	Homo sapiens (human)
26528	DAZ associated protein 1	DAZAP1	Homo sapiens (human)
26524	large tumor suppressor kinase 2	LATS2	Homo sapiens (human)
26523	argonaute RISC component 1	AGO1	Homo sapiens (human)
26519	translocase of inner mitochondrial membrane 10	TIMM10	Homo sapiens (human)
26512	integrator complex subunit 6	INTS6	Homo sapiens (human)
26509	myoferlin	MYOF	Homo sapiens (human)
26505	cyclin and CBS domain divalent metal cation transport mediator 3	CNNM3	Homo sapiens (human)
26504	cyclin and CBS domain divalent metal cation transport mediator 4	CNNM4	Homo sapiens (human)
26503	solute carrier family 17 member 5	SLC17A5 Aliases: AST ISSD NSD SD SIALIN SLD Salla disease acidic sugar transporter infantile sialic acid storage disorder	Homo sapiens (human)	Alzheimer's disease Balo concentric sclerosis Crimean-Congo hemorrhagic fever Gilbert syndrome HELLP syndrome IgA glomerulonephritis Japanese encephalitis Lassa fever Parkinson's disease Plasmodium falciparum malaria Reye syndrome Stevens-Johnson syndrome Wilson disease abdominal obesity-metabolic syndrome 1 acrodermatitis acute pancreatitis adrenoleukodystrophy agammaglobulinemia agranulocytosis alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis allergic asthma alternating exotropia amelogenesis imperfecta type 1E amnestic disorder amyotrophic lateral sclerosis type 1 anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis autoimmune hepatitis autoimmune polyendocrine syndrome bilirubin metabolic disorder cancer cardiovascular system disease cataract 2 multiple types cataract 30 cataract 32 multiple types central nervous system disease cerebral degeneration cerebral infarction cerebrovascular disease cholestasis chromosome 17p13.1 deletion syndrome chronic kidney disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer common cold communicating hydrocephalus congenital nystagmus congenital ptosis congestive heart failure coronary artery disease dementia dengue disease dengue hemorrhagic fever depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis diarrhea disease of metabolism disseminated intravascular coagulation dissociated nystagmus dysthymic disorder embryoma epilepsy essential hypertension essential thrombocythemia exotropia familial hyperlipidemia familial nephrotic syndrome fascioliasis fibromyalgia gallbladder disease gingival hypertrophy gingival overgrowth glomerulonephritis glucose intolerance glycogen storage disease II head and neck squamous cell carcinoma heart disease hemochromatosis hepatitis A hepatitis B hepatitis C hepatitis hepatocellular carcinoma hydrocephalus hyperglycemia hypertension hypohidrotic ectodermal dysplasia immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome intellectual disability intrahepatic cholestasis of pregnancy intrinsic asthma iron metabolism disease kidney disease kidney failure large intestine cancer late onset Parkinson's disease learning disability leukodystrophy leukopenia lipoid nephrosis lissencephaly liver cancer liver carcinoma liver cirrhosis liver disease lung cancer lung non-small cell carcinoma lymphopenia lysosomal storage disease macrocytic anemia major depressive disorder medium chain acyl-CoA dehydrogenase deficiency melancholic depression melanoma microphthalmia monocular exotropia myelodysplastic syndrome myocarditis myositis narcolepsy nasopharyngitis nephritis nephrosis nephrotic syndrome neurodegenerative disease neurotic disorder neutropenia obesity obsolete Matthew-Wood syndrome obsolete melancholia obstructive hydrocephalus obstructive sleep apnea osteoarthritis osteomalacia pancreatitis pancytopenia parapsoriasis pathologic nystagmus pneumonia portal vein thrombosis pre-eclampsia prediabetes syndrome primary polycythemia primary sclerosing cholangitis psoriasis ptosis purpura fulminans pustulosis of palm and sole pyoureter retrograde amnesia rheumatoid arthritis rickets sclerosing cholangitis senile degeneration of brain severe congenital neutropenia sialuria sickle cell anemia skin melanoma spontaneous ocular nystagmus steatotic liver disease subcortical band heterotopia thrombocytopenia tuberculosis type 2 diabetes mellitus uremia viral infectious disease visceral leishmaniasis visual epilepsy yellow fever
26496	olfactory receptor family 10 subfamily A member 3	OR10A3	Homo sapiens (human)
26494	olfactory receptor family 8 subfamily G member 1	OR8G1	Homo sapiens (human)
26493	olfactory receptor family 8 subfamily B member 8	OR8B8	Homo sapiens (human)
26476	olfactory receptor family 10 subfamily J member 1	OR10J1	Homo sapiens (human)
26470	seizure related 6 homolog like 2	SEZ6L2	Homo sapiens (human)
26464	vanin 3	Vnn3	Mus musculus (house mouse)

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

LM-GlycoRepo

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements