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