abnormality of renal resorption Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	An abnormality of renal absorption. (Human Phenotype Ontology, HP_0011038)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0011038
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Genes

18 genes associated with the abnormality of renal resorption phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
CEP290	centrosomal protein 290kDa
CLCNKB	chloride channel, voltage-sensitive Kb
COA5	cytochrome c oxidase assembly factor 5
COX10	COX10 heme A:farnesyltransferase cytochrome c oxidase assembly factor
COX14	COX14 cytochrome c oxidase assembly factor
COX20	COX20 cytochrome c oxidase assembly factor
COX6B1	cytochrome c oxidase subunit VIb polypeptide 1 (ubiquitous)
CTNS	cystinosin, lysosomal cystine transporter
FAH	fumarylacetoacetate hydrolase (fumarylacetoacetase)
FAM20A	family with sequence similarity 20, member A
FASTKD2	FAST kinase domains 2
FGF23	fibroblast growth factor 23
GALNT3	polypeptide N-acetylgalactosaminyltransferase 3
HBB	hemoglobin, beta
KL	klotho
OCRL	oculocerebrorenal syndrome of Lowe
PET100	PET100 homolog (S. cerevisiae)
TACO1	translational activator of mitochondrially encoded cytochrome c oxidase I