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)