renal hypoplasia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Hypoplasia of the kidney. (Human Phenotype Ontology, HP_0000089)
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32 genes associated with the renal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATRX alpha thalassemia/mental retardation syndrome X-linked
BMP4 bone morphogenetic protein 4
CHD7 chromodomain helicase DNA binding protein 7
DCHS1 dachsous cadherin-related 1
DHCR7 7-dehydrocholesterol reductase
FAT4 FAT atypical cadherin 4
FRAS1 Fraser extracellular matrix complex subunit 1
FREM2 FRAS1 related extracellular matrix protein 2
GLI3 GLI family zinc finger 3
GRIP1 glutamate receptor interacting protein 1
HNF1B HNF1 homeobox B
JAG1 jagged 1
KCTD1 potassium channel tetramerization domain containing 1
LRP4 low density lipoprotein receptor-related protein 4
MUC1 mucin 1, cell surface associated
NAA10 N(alpha)-acetyltransferase 10, NatA catalytic subunit
NIPBL Nipped-B homolog (Drosophila)
PAX2 paired box 2
PDE6D phosphodiesterase 6D, cGMP-specific, rod, delta
PIEZO2 piezo-type mechanosensitive ion channel component 2
PQBP1 polyglutamine binding protein 1
PTEN phosphatase and tensin homolog
PUF60 poly-U binding splicing factor 60KDa
RAB40AL RAB40A, member RAS oncogene family-like
REN renin
RNU4ATAC RNA, U4atac small nuclear (U12-dependent splicing)
ROBO2 roundabout, axon guidance receptor, homolog 2 (Drosophila)
SALL1 spalt-like transcription factor 1
SALL4 spalt-like transcription factor 4
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
STRA6 stimulated by retinoic acid 6
WDR19 WD repeat domain 19