abnormal cardiac mesenchyme morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the embryonic connective tissue made up of loosely aggregated mesenchymal cells, supported by interlaminar jelly, that gives rise to the developing cardiac structures (Mammalian Phenotype Ontology, MP_0011264)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011264
Similar Terms
Downloads & Tools

Genes

3 gene mutations causing the abnormal cardiac mesenchyme morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ANKRD17 ankyrin repeat domain 17
BMP4 bone morphogenetic protein 4
ITGB1 integrin, beta 1 (fibronectin receptor, beta polypeptide, antigen CD29 includes MDF2, MSK12)