absent myotome Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the mesoderm that is derived from the somite that is fated to become the musculature (Mammalian Phenotype Ontology, MP_0012249)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012249
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3 gene mutations causing the absent myotome phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
MECOM MDS1 and EVI1 complex locus
MYF5 myogenic factor 5
TCF15 transcription factor 15 (basic helix-loop-helix)