caudal vertebral fusion Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description the union of one or more caudal vertebrae into a single structure in species where this does not normally occur (Mammalian Phenotype Ontology, MP_0004619)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004619
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Genes

12 gene mutations causing the caudal vertebral fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ANKRD13A ankyrin repeat domain 13A
AXIN1 axin 1
CENPJ centromere protein J
DMRT2 doublesex and mab-3 related transcription factor 2
FGF3 fibroblast growth factor 3
FGFR2 fibroblast growth factor receptor 2
LRP6 low density lipoprotein receptor-related protein 6
NRARP NOTCH-regulated ankyrin repeat protein
PPP5C protein phosphatase 5, catalytic subunit
ROR2 receptor tyrosine kinase-like orphan receptor 2
RPL24 ribosomal protein L24
RPL38 ribosomal protein L38