abnormal vertebral transverse process morphology Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	any structural anomaly of the bony protrusions on either side of the arch of a vertebrae at the point where the lamina joins the pedicle, between the superior and inferior articular processes; muscles and ligaments attach to these processes (Mammalian Phenotype Ontology, MP_0004600)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004600
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Genes

12 gene mutations causing the abnormal vertebral transverse process morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
FOXC1	forkhead box C1
FTO	fat mass and obesity associated
HOXD10	homeobox D10
MESP2	mesoderm posterior basic helix-loop-helix transcription factor 2
MYSM1	Myb-like, SWIRM and MPN domains 1
PAX1	paired box 1
RPL38	ribosomal protein L38
RPS7	ribosomal protein S7
STARD5	StAR-related lipid transfer (START) domain containing 5
SUPV3L1	suppressor of var1, 3-like 1 (S. cerevisiae)
TBX6	T-box 6
UNCX	UNC homeobox