polycystic kidney Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008528
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Genes

36 gene mutations causing the polycystic kidney phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGTR2 angiotensin II receptor, type 2
B9D1 B9 protein domain 1
BCL2 B-cell CLL/lymphoma 2
BICC1 BicC family RNA binding protein 1
BMP4 bone morphogenetic protein 4
BMP7 bone morphogenetic protein 7
CC2D2A coiled-coil and C2 domain containing 2A
CCDC39 coiled-coil domain containing 39
CEP290 centrosomal protein 290kDa
CLDN16 claudin 16
CXCR4 chemokine (C-X-C motif) receptor 4
CYS1 cystin 1
DCTN5 dynactin 5 (p25)
DNAH11 dynein, axonemal, heavy chain 11
DNM2 dynamin 2
FMN1 formin 1
GLIS3 GLIS family zinc finger 3
GRIP1 glutamate receptor interacting protein 1
IFT88 intraflagellar transport 88
INPP5E inositol polyphosphate-5-phosphatase, 72 kDa
LAMA5 laminin, alpha 5
LGR4 leucine-rich repeat containing G protein-coupled receptor 4
LIN7C lin-7 homolog C (C. elegans)
LTBP1 latent transforming growth factor beta binding protein 1
MKS1 Meckel syndrome, type 1
MTSS1 metastasis suppressor 1
NEK1 NIMA-related kinase 1
NEK8 NIMA-related kinase 8
NPHP3 nephronophthisis 3 (adolescent)
PKD1 polycystic kidney disease 1 (autosomal dominant)
PKD2 polycystic kidney disease 2 (autosomal dominant)
ROBO1 roundabout, axon guidance receptor, homolog 1 (Drosophila)
SDCCAG8 serologically defined colon cancer antigen 8
TMEM67 transmembrane protein 67
TTC21B tetratricopeptide repeat domain 21B
WWTR1 WW domain containing transcription regulator 1