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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 |
|---|---|---|---|
| 8876 | VNN1 | vanin 1 | |
| 8877 | SPHK1 | sphingosine kinase 1 | |
| 8897 | MTMR3 | myotubularin related protein 3 | |
| 9173 | IL1RL1 | interleukin 1 receptor like 1 | |
| 9415 | FADS2 | fatty acid desaturase 2 | |
| 9420 | CYP7B1 | cytochrome P450 family 7 subfamily B member 1 | |
| 9435 | CHST2 | carbohydrate sulfotransferase 2 | |
| 9468 | PCYT1B | phosphate cytidylyltransferase 1B, choline | |
| 9514 | GAL3ST1 | galactose-3-O-sulfotransferase 1 | |
| 9663 | LPIN2 | lipin 2 |
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 |
