absent scrotum Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Congenital absence of the scrotum. (Human Phenotype Ontology, HP_0008707)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002670
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4 gene mutations causing the absent scrotum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AR androgen receptor
CYP11A1 cytochrome P450, family 11, subfamily A, polypeptide 1
FOXP3 forkhead box P3
HOXA10 homeobox A10