abnormal dorsal-ventral axis patterning Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the development or formation of the axis that runs from the front to the back surface of the body (Mammalian Phenotype Ontology, MP_0001704)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001704
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18 gene mutations causing the abnormal dorsal-ventral axis patterning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
C2CD3 C2 calcium-dependent domain containing 3
CHMP5 charged multivesicular body protein 5
FKBP8 FK506 binding protein 8, 38kDa
FURIN furin (paired basic amino acid cleaving enzyme)
G3BP1 GTPase activating protein (SH3 domain) binding protein 1
GATA4 GATA binding protein 4
GPR161 G protein-coupled receptor 161
GRHL3 grainyhead-like 3 (Drosophila)
NF2 neurofibromin 2 (merlin)
OVOL2 ovo-like zinc finger 2
PBX1 pre-B-cell leukemia homeobox 1
SHH sonic hedgehog
SUFU suppressor of fused homolog (Drosophila)
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
TFAP2C transcription factor AP-2 gamma (activating enhancer binding protein 2 gamma)
TMEM67 transmembrane protein 67
USP8 ubiquitin specific peptidase 8
YAP1 Yes-associated protein 1