abnormal sex determination Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Anomaly of primary or secondary sexual development or characteristics. (Human Phenotype Ontology, HP_0012244)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012244
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9 genes associated with the abnormal sex determination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AKR1C2 aldo-keto reductase family 1, member C2
CBX2 chromobox homolog 2
CYP11A1 cytochrome P450, family 11, subfamily A, polypeptide 1
DHH desert hedgehog
MAP3K1 mitogen-activated protein kinase kinase kinase 1, E3 ubiquitin protein ligase
NR0B1 nuclear receptor subfamily 0, group B, member 1
SOX9 SRY (sex determining region Y)-box 9
SRY sex determining region Y
WNT4 wingless-type MMTV integration site family, member 4