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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 |
|---|---|---|---|
| 64116 | SLC39A8 | solute carrier family 39 member 8 | |
| 64581 | CLEC7A | C-type lectin domain containing 7A | |
| 79947 | DHDDS | dehydrodolichyl diphosphate synthase subunit | |
| 80329 | ULBP1 | UL16 binding protein 1 | |
| 80896 | NPL | N-acetylneuraminate pyruvate lyase | |
| 91869 | RFT1 | RFT1 homolog | |
| 92579 | G6PC3 | glucose-6-phosphatase catalytic subunit 3 | |
| 93210 | PGAP3 | post-GPI attachment to proteins phospholipase 3 | |
| 130367 | SGPP2 | sphingosine-1-phosphate phosphatase 2 | |
| 130589 | GALM | galactose mutarotase |
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 |
