abnormal vagina development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description abnormal morphogenesis of the female reproductive canal located between the uterus and the vulva (Mammalian Phenotype Ontology, MP_0003531)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003531
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2 gene mutations causing the abnormal vagina development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
LHCGR luteinizing hormone/choriogonadotropin receptor
LHFPL2 lipoma HMGIC fusion partner-like 2