dystrophic cardiac calcinosis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description a condition characterized by the localized deposition of calcium salts in the heart; often occurring in association with inflammation or atherosclerotic lesions and other pathological states (Mammalian Phenotype Ontology, MP_0002837)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002837
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13 gene mutations causing the dystrophic cardiac calcinosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCC6 ATP-binding cassette, sub-family C (CFTR/MRP), member 6
DES desmin
DNM1L dynamin 1-like
GSTZ1 glutathione S-transferase zeta 1
MMP9 matrix metallopeptidase 9
MYBPC3 myosin binding protein C, cardiac
MYH6 myosin, heavy chain 6, cardiac muscle, alpha
MYL2 myosin, light chain 2, regulatory, cardiac, slow
NOV nephroblastoma overexpressed
PIK3R1 phosphoinositide-3-kinase, regulatory subunit 1 (alpha)
SCG5 secretogranin V
SGCD sarcoglycan, delta (35kDa dystrophin-associated glycoprotein)
SLC2A4 solute carrier family 2 (facilitated glucose transporter), member 4