abnormality of the renal cortex Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the cortex of the kidney. (Human Phenotype Ontology, HP_0011035)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011035
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19 genes associated with the abnormality of the renal cortex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCD3 ATP-binding cassette, sub-family D (ALD), member 3
BSND barttin CLCNK-type chloride channel accessory beta subunit
CD96 CD96 molecule
CEP290 centrosomal protein 290kDa
ETFA electron-transfer-flavoprotein, alpha polypeptide
ETFB electron-transfer-flavoprotein, beta polypeptide
ETFDH electron-transferring-flavoprotein dehydrogenase
INVS inversin
MUC1 mucin 1, cell surface associated
NEK8 NIMA-related kinase 8
NIPBL Nipped-B homolog (Drosophila)
NPHP1 nephronophthisis 1 (juvenile)
NPHP3 nephronophthisis 3 (adolescent)
NPHP4 nephronophthisis 4
PEX1 peroxisomal biogenesis factor 1
PKHD1 polycystic kidney and hepatic disease 1 (autosomal recessive)
TMEM67 transmembrane protein 67
TTC37 tetratricopeptide repeat domain 37
XPNPEP3 X-prolyl aminopeptidase 3, mitochondrial