Bladder Exstrophy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Eversion of the posterior bladder wall through the congenitally absent lower anterior abdominal wall and anterior bladder wall (Human Phenotype Ontology, HP_0002836)
External Link https://www.disgenet.org/browser/0/1/0/C0005689
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Genes

16 genes associated with the disease Bladder Exstrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CCN1 cellular communication network factor 1
CDH11 cadherin 11, type 2, OB-cadherin (osteoblast)
CNTNAP3 contactin associated protein-like 3
IL13 interleukin 13
IL18 interleukin 18
ISL1 ISL LIM homeobox 1
KRAS Kirsten rat sarcoma viral oncogene homolog
LZTR1 leucine-zipper-like transcription regulator 1
MEGF6 multiple EGF-like-domains 6
PAH phenylalanine hydroxylase
PLAGL1 pleiomorphic adenoma gene-like 1
PREX2 phosphatidylinositol-3,4,5-trisphosphate-dependent Rac exchange factor 2
TP63 tumor protein p63
UPB1 ureidopropionase, beta
WNT3 wingless-type MMTV integration site family, member 3
WNT9B wingless-type MMTV integration site family, member 9B