| Dataset | MPO Gene-Phenotype Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | missing portion of the small intestine that extends from the duodenum to the ileum (Mammalian Phenotype Ontology, MP_0000498) |
| External Link | http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000498 |
| Similar Terms | |
| Downloads & Tools |
1 gene mutations causing the absent jejunum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol | Name |
|---|---|
| CDKN1C | cyclin-dependent kinase inhibitor 1C (p57, Kip2) |
