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 **7976 - 8000** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▲	Organism	Disease Ontology
6568	solute carrier family 17 member 1	SLC17A1	Homo sapiens (human)
10246	solute carrier family 17 member 2	SLC17A2	Homo sapiens (human)
10786	solute carrier family 17 member 3	SLC17A3	Homo sapiens (human)
10050	solute carrier family 17 member 4	SLC17A4	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
57084	solute carrier family 17 member 6	SLC17A6	Homo sapiens (human)
246213	solute carrier family 17 member 8	SLC17A8	Homo sapiens (human)
6570	solute carrier family 18 member A1	SLC18A1	Homo sapiens (human)
6571	solute carrier family 18 member A2	SLC18A2	Homo sapiens (human)
6572	solute carrier family 18 member A3	SLC18A3	Homo sapiens (human)
6573	solute carrier family 19 member 1	SLC19A1	Homo sapiens (human)
10560	solute carrier family 19 member 2	SLC19A2	Homo sapiens (human)
80704	solute carrier family 19 member 3	SLC19A3	Homo sapiens (human)
6505	solute carrier family 1 member 1	SLC1A1	Homo sapiens (human)
6506	solute carrier family 1 member 2	SLC1A2	Homo sapiens (human)
6507	solute carrier family 1 member 3	SLC1A3	Homo sapiens (human)
6509	solute carrier family 1 member 4	SLC1A4	Homo sapiens (human)
6510	solute carrier family 1 member 5	SLC1A5	Homo sapiens (human)
6511	solute carrier family 1 member 6	SLC1A6	Homo sapiens (human)
6512	solute carrier family 1 member 7	SLC1A7	Homo sapiens (human)
6574	solute carrier family 20 member 1	SLC20A1	Homo sapiens (human)
6575	solute carrier family 20 member 2	SLC20A2	Homo sapiens (human)
6580	solute carrier family 22 member 1	SLC22A1	Homo sapiens (human)
387775	solute carrier family 22 member 10	SLC22A10	Homo sapiens (human)
55867	solute carrier family 22 member 11	SLC22A11	Homo sapiens (human)

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