gonadal ridge hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description underdevelopment or reduced size of the elevation of thickened mesothelium and underlying mesenchyme found on the ventromedial border of the embryonic mesonephros, usually due to reduced cell number; normally, primordial germ cells become embedded in it, establishing it as the primordium of the testis or ovary (Mammalian Phenotype Ontology, MP_0011412)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011412
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Genes

3 gene mutations causing the gonadal ridge hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
EMX2 empty spiracles homeobox 2
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
OSR1 odd-skipped related transciption factor 1