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 **8651 - 8675** of **9988** in total

« First

‹ Prev

…

343

344

345

346

347

348

349

350

351

…

Next ›

Last »
Gene ID	Gene Name ▲	Gene Symbol	Organism	Disease Ontology
2542	solute carrier family 37 member 4	SLC37A4 Aliases: G6PT GSD1b GSD1c GSD1d Glucose-6-phosphate exchanger SLC37A4 SPX4 glucose-6-phosphatase transporter sugar-phosphate exchange protein 4	Homo sapiens (human)	Gerstmann-Straussler-Scheinker syndrome Gorham's disease Laron syndrome achondroplasia acute pancreatitis agranulocytosis aphthous stomatitis autoimmune disease autoimmune lymphoproliferative syndrome brain cancer cancer central nervous system cancer congenital disorder of glycosylation type II cystinuria diabetes mellitus diabetic ketoacidosis disease of metabolism embryoma essential hypertension eyelid disease familial hyperlipidemia focal segmental glomerulosclerosis galactosemia giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease Ib glycogen storage disease Ic glycogen storage disease gout hepatoblastoma hepatocellular carcinoma high grade glioma hypertension hyperuricemia hypoglycemia immune system disease inherited metabolic disorder kidney disease kidney failure kwashiorkor lactic acidosis leukopenia liver cancer marasmus mixed glioma nephritis nephrolithiasis nephrosis neutropenia nutrition disease obesity obsolete type 1 diabetes mellitus 9 osteoporosis pancreatitis polycystic ovary syndrome primary pulmonary hypertension protein-energy malnutrition proteinuria pyoureter severe congenital neutropenia sudden infant death syndrome type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus uric acid nephrolithiasis xanthomatosis
81539	solute carrier family 38 member 1	SLC38A1	Homo sapiens (human)
124565	solute carrier family 38 member 10	SLC38A10	Homo sapiens (human)
151258	solute carrier family 38 member 11	SLC38A11	Homo sapiens (human)
54407	solute carrier family 38 member 2	SLC38A2	Homo sapiens (human)
10991	solute carrier family 38 member 3	SLC38A3	Homo sapiens (human)
55089	solute carrier family 38 member 4	SLC38A4	Homo sapiens (human)
92745	solute carrier family 38 member 5	SLC38A5	Homo sapiens (human)
145389	solute carrier family 38 member 6	SLC38A6	Homo sapiens (human)
153129	solute carrier family 38 member 9	SLC38A9	Homo sapiens (human)
57181	solute carrier family 39 member 10	SLC39A10	Homo sapiens (human)
23516	solute carrier family 39 member 14	SLC39A14	Homo sapiens (human)	hypermanganesemia with dystonia 2
55630	solute carrier family 39 member 4	SLC39A4	Homo sapiens (human)
283375	solute carrier family 39 member 5	SLC39A5	Homo sapiens (human)
25800	solute carrier family 39 member 6	SLC39A6	Homo sapiens (human)
7922	solute carrier family 39 member 7	SLC39A7	Homo sapiens (human)
64116	solute carrier family 39 member 8	SLC39A8 Aliases: BCG-induced integral membrane protein in monocyte clone 103 BIGM103 Metal cation symporter ZIP8 ZIP-8 ZIP8 ZRT/IRT-like protein 8 Zinc transporter ZIP8	Homo sapiens (human)	Crohn's colitis Crohn's disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Laron syndrome Leigh disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Wilson disease achondroplasia acute chest syndrome alcohol dependence alcohol use disorder alternating hemiplegia of childhood androgen insensitivity syndrome anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy astigmatism atherosclerosis atrial fibrillation attention deficit hyperactivity disorder autonomic neuropathy bacterial sepsis breast cancer breast carcinoma cancer central nervous system disease cerebral infarction cerebrovascular disease childhood leukemia colorectal cancer colorectal carcinoma congenital disorder of glycosylation Ii congenital disorder of glycosylation In congenital disorder of glycosylation type I congenital disorder of glycosylation type IIn congenital disorder of glycosylation congenital nystagmus congestive heart failure coronary artery disease craniosynostosis dermatitis diabetes mellitus diabetic ketoacidosis dissociated nystagmus dystonia epilepsy essential hypertension focal hand dystonia generalized dystonia hemochromatosis hydrocephalus hyperopia hypertension hypertropia idiopathic scoliosis inflammatory bowel disease 1 inflammatory bowel disease intellectual disability iron metabolism disease kwashiorkor large intestine cancer learning disability left ventricular noncompaction leukemia macrocytic anemia marasmus mechanical strabismus mitochondrial metabolism disease mitochondrial myopathy nervous system disease neuroblastoma nicotine dependence nutrition disease obsolete infantile epileptic encephalopathy ophthalmoplegia osteoarthritis pathologic nystagmus protein-energy malnutrition pulmonary tuberculosis schizophrenia sensorineural hearing loss spontaneous ocular nystagmus strabismus systemic lupus erythematosus tuberculosis tuberculous pneumothorax type 2 diabetes mellitus ulcerative colitis visual epilepsy
55334	solute carrier family 39 member 9	SLC39A9	Homo sapiens (human)
6521	solute carrier family 4 member 1 (Diego blood group)	SLC4A1	Homo sapiens (human)
22950	solute carrier family 4 member 1 adaptor protein	SLC4A1AP	Homo sapiens (human)
57282	solute carrier family 4 member 10	SLC4A10	Homo sapiens (human)
83959	solute carrier family 4 member 11	SLC4A11	Homo sapiens (human)
6522	solute carrier family 4 member 2	SLC4A2	Homo sapiens (human)
8671	solute carrier family 4 member 4	SLC4A4	Homo sapiens (human)
57835	solute carrier family 4 member 5	SLC4A5	Homo sapiens (human)

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