absent ovary Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Aplasia, that is failure to develop, of the ovary. (Human Phenotype Ontology, HP_0010463)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003578
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Genes

9 gene mutations causing the absent ovary phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CPEB1 cytoplasmic polyadenylation element binding protein 1
EMX2 empty spiracles homeobox 2
LHX1 LIM homeobox 1
LHX9 LIM homeobox 9
NR5A1 nuclear receptor subfamily 5, group A, member 1
OSR1 odd-skipped related transciption factor 1
TET1 tet methylcytosine dioxygenase 1
TP63 tumor protein p63
WT1 Wilms tumor 1