True Hermaphroditism (Disorder) Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0266361
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Genes

27 genes associated with the disease True Hermaphroditism (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AMH anti-Mullerian hormone
AR androgen receptor
B9D1 B9 protein domain 1
B9D2 B9 protein domain 2
CC2D2A coiled-coil and C2 domain containing 2A
CEP290 centrosomal protein 290kDa
CEP55 centrosomal protein 55kDa
COX7B cytochrome c oxidase subunit VIIb
CSPP1 centrosome and spindle pole associated protein 1
GNRH2 gonadotropin-releasing hormone 2
HCCS holocytochrome c synthase
MKS1 Meckel syndrome, type 1
NDUFB11 NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 11, 17.3kDa
NR5A1 nuclear receptor subfamily 5, group A, member 1
RPGRIP1 retinitis pigmentosa GTPase regulator interacting protein 1
RPGRIP1L RPGRIP1-like
RSPO1 R-spondin 1
SOX9 SRY (sex determining region Y)-box 9
SRY sex determining region Y
TCTN2 tectonic family member 2
TMEM107 transmembrane protein 107
TMEM216 transmembrane protein 216
TMEM231 transmembrane protein 231
TMEM67 transmembrane protein 67
WDPCP WD repeat containing planar cell polarity effector
WNT4 wingless-type MMTV integration site family, member 4
WT1 Wilms tumor 1