renal hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Hypoplasia of the kidney. (Human Phenotype Ontology, HP_0000089)
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37 gene mutations causing the renal hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACVR2B activin A receptor, type IIB
AGTR2 angiotensin II receptor, type 2
ALDH1A2 aldehyde dehydrogenase 1 family, member A2
ARHGAP1 Rho GTPase activating protein 1
BAG6 BCL2-associated athanogene 6
BCL2 B-cell CLL/lymphoma 2
BMP4 bone morphogenetic protein 4
BMP7 bone morphogenetic protein 7
CRIM1 cysteine rich transmembrane BMP regulator 1 (chordin-like)
DLG1 discs, large homolog 1 (Drosophila)
DNAH5 dynein, axonemal, heavy chain 5
ETV4 ets variant 4
EYA1 EYA transcriptional coactivator and phosphatase 1
GATA2 GATA binding protein 2
GDNF glial cell derived neurotrophic factor
GREM1 gremlin 1, DAN family BMP antagonist
HOXA13 homeobox A13
IGF2BP1 insulin-like growth factor 2 mRNA binding protein 1
ILK integrin-linked kinase
LGR4 leucine-rich repeat containing G protein-coupled receptor 4
MEGF8 multiple EGF-like-domains 8
NOS3 nitric oxide synthase 3 (endothelial cell)
NOTCH2 notch 2
PAX2 paired box 2
PBX1 pre-B-cell leukemia homeobox 1
PDS5A PDS5 cohesin associated factor A
RDH10 retinol dehydrogenase 10 (all-trans)
RET ret proto-oncogene
SALL1 spalt-like transcription factor 1
SALL4 spalt-like transcription factor 4
SIX1 SIX homeobox 1
SIX2 SIX homeobox 2
SLIT3 slit homolog 3 (Drosophila)
TCF21 transcription factor 21
TFCP2L1 transcription factor CP2-like 1
TP53 tumor protein p53
WNT11 wingless-type MMTV integration site family, member 11