abnormal myotome morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the mesoderm that is derived from the somite that is fated to become the musculature (Mammalian Phenotype Ontology, MP_0003939)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003939
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8 gene mutations causing the abnormal myotome morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
DMRT2 doublesex and mab-3 related transcription factor 2
MECOM MDS1 and EVI1 complex locus
MYF5 myogenic factor 5
MYF6 myogenic factor 6 (herculin)
PAX3 paired box 3
PDGFRA platelet-derived growth factor receptor, alpha polypeptide
RIPPLY2 ripply transcriptional repressor 2
TCF15 transcription factor 15 (basic helix-loop-helix)