ectopic kidney Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A developmental defect in which a kidney is located in an abnormal anatomic position. (Human Phenotype Ontology, HP_0000086)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000086
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Genes

15 genes associated with the ectopic kidney phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CCBE1 collagen and calcium binding EGF domains 1
DNA2 DNA replication helicase/nuclease 2
FANCA Fanconi anemia, complementation group A
FANCC Fanconi anemia, complementation group C
FANCD2 Fanconi anemia, complementation group D2
FANCE Fanconi anemia, complementation group E
GLI3 GLI family zinc finger 3
HOXD13 homeobox D13
JAM3 junctional adhesion molecule 3
KMT2D lysine (K)-specific methyltransferase 2D
NIPBL Nipped-B homolog (Drosophila)
RBBP8 retinoblastoma binding protein 8
SALL4 spalt-like transcription factor 4
SLX4 SLX4 structure-specific endonuclease subunit
STRA6 stimulated by retinoic acid 6