renal malrotation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the normal developmental rotation of the kidney leading to an abnormal orientation of the kidney. (Human Phenotype Ontology, HP_0004712)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004712
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Genes

5 genes associated with the renal malrotation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
EYA1 EYA transcriptional coactivator and phosphatase 1
PAX2 paired box 2
RBM8A RNA binding motif protein 8A
SALL4 spalt-like transcription factor 4
STRA6 stimulated by retinoic acid 6