Bifid Scrotum Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Midline indentation or cleft of the scrotum. (Human Phenotype Ontology, HP_0000048)
External Link https://www.disgenet.org/browser/0/1/0/C0341787
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Genes

29 genes associated with the disease Bifid Scrotum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AR androgen receptor
BUB1B BUB1 mitotic checkpoint serine/threonine kinase B
CDH11 cadherin 11, type 2, OB-cadherin (osteoblast)
CHD7 chromodomain helicase DNA binding protein 7
COLEC10 collectin sub-family member 10 (C-type lectin)
CYB5A cytochrome b5 type A (microsomal)
DACT1 dishevelled-binding antagonist of beta-catenin 1
DHCR7 7-dehydrocholesterol reductase
FAT4 FAT atypical cadherin 4
FGFR2 fibroblast growth factor receptor 2
FZD2 frizzled class receptor 2
HOXA13 homeobox A13
HOXD13 homeobox D13
HSD3B2 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2
IRF6 interferon regulatory factor 6
KIFBP kinesin family binding protein
MAMLD1 mastermind-like domain containing 1
MNX1 motor neuron and pancreas homeobox 1
MTM1 myotubularin 1
MYRF myelin regulatory factor
NR5A1 nuclear receptor subfamily 5, group A, member 1
POR P450 (cytochrome) oxidoreductase
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
SPECC1L sperm antigen with calponin homology and coiled-coil domains 1-like
SRD5A2 steroid-5-alpha-reductase, alpha polypeptide 2 (3-oxo-5 alpha-steroid delta 4-dehydrogenase alpha 2)
SRY sex determining region Y
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)