abnormal kidney cell proliferation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the ability of any kidney cell population to undergo expansion by cell division (Mammalian Phenotype Ontology, MP_0011439)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011439
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Genes

23 gene mutations causing the abnormal kidney cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ALMS1 Alstrom syndrome protein 1
BAG6 BCL2-associated athanogene 6
BCL2 B-cell CLL/lymphoma 2
CLDN4 claudin 4
FAS Fas cell surface death receptor
FAT4 FAT atypical cadherin 4
FGFRL1 fibroblast growth factor receptor-like 1
GADD45A growth arrest and DNA-damage-inducible, alpha
GAS6 growth arrest-specific 6
GDNF glial cell derived neurotrophic factor
MKS1 Meckel syndrome, type 1
MMP14 matrix metallopeptidase 14 (membrane-inserted)
MTA2 metastasis associated 1 family, member 2
MTSS1 metastasis suppressor 1
NFE2L2 nuclear factor, erythroid 2-like 2
NOS3 nitric oxide synthase 3 (endothelial cell)
NOTCH2 notch 2
PDGFRB platelet-derived growth factor receptor, beta polypeptide
PKD1 polycystic kidney disease 1 (autosomal dominant)
PKD2 polycystic kidney disease 2 (autosomal dominant)
PKHD1 polycystic kidney and hepatic disease 1 (autosomal recessive)
POU3F3 POU class 3 homeobox 3
RRM2B ribonucleotide reductase M2 B (TP53 inducible)