abnormal dermomyotome development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the portion of the embryonic somite that remains after migration of the sclerotomic tissue (Mammalian Phenotype Ontology, MP_0004206)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004206
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9 gene mutations causing the abnormal dermomyotome development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APH1A APH1A gamma secretase subunit
DISP1 dispatched homolog 1 (Drosophila)
DLL3 delta-like 3 (Drosophila)
DMRT2 doublesex and mab-3 related transcription factor 2
MESP2 mesoderm posterior basic helix-loop-helix transcription factor 2
PAX3 paired box 3
PRDM1 PR domain containing 1, with ZNF domain
RTEL1 regulator of telomere elongation helicase 1
WDR19 WD repeat domain 19