abnormal vertebral arch development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomalous formation of the posterior projection from the body of a vertebra that encloses the vertebral foramen (Mammalian Phenotype Ontology, MP_0005226)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005226
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24 gene mutations causing the abnormal vertebral arch development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APAF1 apoptotic peptidase activating factor 1
BMPER BMP binding endothelial regulator
CHRD chordin
FKBP8 FK506 binding protein 8, 38kDa
FOXC2 forkhead box C2
LASP1 LIM and SH3 protein 1
LMX1A LIM homeobox transcription factor 1, alpha
LRP6 low density lipoprotein receptor-related protein 6
NKX3-2 NK3 homeobox 2
NOG noggin
PAX1 paired box 1
PDGFC platelet derived growth factor C
PKD1 polycystic kidney disease 1 (autosomal dominant)
RAB23 RAB23, member RAS oncogene family
RAI1 retinoic acid induced 1
SUZ12 SUZ12 polycomb repressive complex 2 subunit
T T, brachyury homolog (mouse)
TBX6 T-box 6
TGFB2 transforming growth factor, beta 2
TRAF4 TNF receptor-associated factor 4
TRPM6 transient receptor potential cation channel, subfamily M, member 6
TULP3 tubby like protein 3
TWSG1 twisted gastrulation BMP signaling modulator 1
VANGL2 VANGL planar cell polarity protein 2