short vertebral body Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced length of the main cylindrical portion of the vertebra ventral to the vertebral canal (Mammalian Phenotype Ontology, MP_0004706)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004706
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Genes

5 gene mutations causing the short vertebral body phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CACNA2D2 calcium channel, voltage-dependent, alpha 2/delta subunit 2
COL1A1 collagen, type I, alpha 1
FGFR3 fibroblast growth factor receptor 3
FOXC2 forkhead box C2
LASP1 LIM and SH3 protein 1