absent sclerotome Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the group of mesenchymal cells that emerge from the ventromedial part of a somite and migrate toward the notochord to give rise to the ribs and vertebrae (Mammalian Phenotype Ontology, MP_0006295)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006295
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Genes

3 gene mutations causing the absent sclerotome phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
MECOM MDS1 and EVI1 complex locus
PAX1 paired box 1
TCF15 transcription factor 15 (basic helix-loop-helix)