absent vas deferens Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Aplasia (congenital absence) of the vas deferens. (Human Phenotype Ontology, HP_0012873)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003557
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5 gene mutations causing the absent vas deferens phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AR androgen receptor
EMX2 empty spiracles homeobox 2
LAMC1 laminin, gamma 1 (formerly LAMB2)
PAX2 paired box 2
WNT9B wingless-type MMTV integration site family, member 9B