Urethral Atresia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Congenital anomaly characterized by closure or failure to develop an opening in the urethra. (Human Phenotype Ontology, HP_0000068)
External Link https://www.disgenet.org/browser/0/1/0/C1610065
Similar Terms
Downloads & Tools

Genes

23 genes associated with the disease Urethral Atresia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
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
CSPP1 centrosome and spindle pole associated protein 1
FANCB Fanconi anemia, complementation group B
FOXF1 forkhead box F1
FRAS1 Fraser extracellular matrix complex subunit 1
FREM2 FRAS1 related extracellular matrix protein 2
GRIP1 glutamate receptor interacting protein 1
MKS1 Meckel syndrome, type 1
RPGRIP1 retinitis pigmentosa GTPase regulator interacting protein 1
RPGRIP1L RPGRIP1-like
TCTN2 tectonic family member 2
TMEM107 transmembrane protein 107
TMEM216 transmembrane protein 216
TMEM231 transmembrane protein 231
TMEM67 transmembrane protein 67
TP63 tumor protein p63
WDPCP WD repeat containing planar cell polarity effector
WNT3 wingless-type MMTV integration site family, member 3
ZIC3 Zic family member 3