duplex kidney Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description a kidney that is split into two separate collecting systems; there may be a duplex ureter or a single ureter; may present unilaterally or bilaterally (Mammalian Phenotype Ontology, MP_0004017)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004017
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Genes

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

Symbol Name
BMP4 bone morphogenetic protein 4
C5ORF42 chromosome 5 open reading frame 42
CC2D2A coiled-coil and C2 domain containing 2A
CXCR4 chemokine (C-X-C motif) receptor 4
DNAH11 dynein, axonemal, heavy chain 11
DNAH5 dynein, axonemal, heavy chain 5
DYNC2H1 dynein, cytoplasmic 2, heavy chain 1
FOXC1 forkhead box C1
LZTS2 leucine zipper, putative tumor suppressor 2
MKS1 Meckel syndrome, type 1
NFIA nuclear factor I/A
TBC1D32 TBC1 domain family, member 32
WDPCP WD repeat containing planar cell polarity effector
ZBTB14 zinc finger and BTB domain containing 14