absent hindgut Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the caudal portion of the primitive digestive tube of the embryo (Mammalian Phenotype Ontology, MP_0012086)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012086
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2 gene mutations causing the absent hindgut phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
MIXL1 Mix paired-like homeobox
NR6A1 nuclear receptor subfamily 6, group A, member 1