absent cranial vagina Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the upper third of the female reproductive canal located between the uterus and the vulva, usually due to a developmental arrest or agenesis of the caudal Mullerian ducts (Mammalian Phenotype Ontology, MP_0009072)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009072
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2 gene mutations causing the absent cranial vagina phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
EMX2 empty spiracles homeobox 2
WNT9B wingless-type MMTV integration site family, member 9B