bifid scrotum Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Midline indentation or cleft of the scrotum. (Human Phenotype Ontology, HP_0000048)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000048
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Genes

22 genes associated with the bifid scrotum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AR androgen receptor
BMP4 bone morphogenetic protein 4
BUB1B BUB1 mitotic checkpoint serine/threonine kinase B
CHD7 chromodomain helicase DNA binding protein 7
DHCR7 7-dehydrocholesterol reductase
EPHX1 epoxide hydrolase 1, microsomal (xenobiotic)
FAT4 FAT atypical cadherin 4
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
HOXA13 homeobox A13
HOXD13 homeobox D13
IRF6 interferon regulatory factor 6
MNX1 motor neuron and pancreas homeobox 1
POR P450 (cytochrome) oxidoreductase
RAB40AL RAB40A, member RAS oncogene family-like
SALL1 spalt-like transcription factor 1
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
SOX9 SRY (sex determining region Y)-box 9
SRD5A2 steroid-5-alpha-reductase, alpha polypeptide 2 (3-oxo-5 alpha-steroid delta 4-dehydrogenase alpha 2)
SRY sex determining region Y
UPB1 ureidopropionase, beta
ZEB2 zinc finger E-box binding homeobox 2