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inflammatory bowel disease 1
Summary
- Synonym
-
- IBD1
- Definition
- An inflammatory bowel disease that has_material_basis_in mutations in the NOD2 gene on chromosome 16q12.1.
- Super Class
- inflammatory bowel disease monogenic disease
External Links
- Disease Ontology
- DOID:0110892
- Mondo Disease Ontology
- OMIM
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 23274 | CLEC16A | C-type lectin domain containing 16A | |
| 23545 | ATP6V0A2 | ATPase H+ transporting V0 subunit a2 | |
| 23583 | SMUG1 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | |
| 23600 | AMACR | alpha-methylacyl-CoA racemase | |
| 23659 | PLA2G15 | phospholipase A2 group XV | |
| 27087 | B3GAT1 | beta-1,3-glucuronyltransferase 1 | |
| 27163 | NAAA | N-acylethanolamine acid amidase | |
| 27306 | HPGDS | hematopoietic prostaglandin D synthase | |
| 30835 | CD209 | CD209 molecule | |
| 51363 | CHST15 | carbohydrate sulfotransferase 15 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q99519 | Sialidase-1 | |
| Q99685 | Monoglyceride lipase | |
| Q99798 | Aconitate hydratase, mitochondrial | |
| Q99999 | Galactosylceramide sulfotransferase | |
| Q9BWD1 | Acetyl-CoA acetyltransferase, cytosolic | |
| Q9BXN2 | C-type lectin domain family 7 member A | |
| Q9BZM6 | UL16-binding protein 1 | |
| Q9C0K1 | Metal cation symporter ZIP8 | |
| Q9H3Q3 | Galactose-3-O-sulfotransferase 2 | |
| Q9HAW7 | UDP-glucuronosyltransferase 1A7 |
