absent jejunum Gene Set

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
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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)