This Myh10 mutation was identified in a screen of ENU-induced mutations and may be useful in studies of congenital heart disease.
The Jackson Laboratory cannot guarantee that cryorecovery of G1 sperm from the Bench to Bassinet (B2B) collection will be successful or that the anticipated phenotype or genotype will be obtained. The cryorecovery fee for this effort will not be refunded or prorated if the recovery is unsuccessful or is in any way unsatisfactory. Genotyping will be the responsibility of the Purchaser.
Cecilia Lo, Univ of Pittsburgh School of Medicine
This T-to-C point mutation at position 5503 of the Myh10 (myosin, heavy polypeptide 10, non-muscle) cDNA was identified in an ENU screen for recessive cardiovascular development phenotypes in Dr. Cecilia Lo's laboratory, NHLBI Cardiovascular Development Consortium (CvDC). It was recovered from G1 sperm and associated with the phenotype described described here. Because G1 sperm were cryopreserved, additional incidental mutations are also segregating in this strain.
Homozygotes demonstrate overriding aorta/double outlet right ventricle (DORV) with ventricular septal defect (VSD), atrioventricular septal defect (AVSD), and ventricular myocardial non-compaction. Exencephaly, cleft lip/facial cleft, and micrognathia are also seen.
This ENU-induced mutation was created and maintained on a C57BL/6J genetic background by the NHLBI Cardiovascular Development Consortium (CvDC), Bench to Bassinet Program. A T-to-C single point mutation at position 1054 of the cDNA (c.T1054C, NM_175260) was discovered through whole exome, high throughput sequencing. This mutation is predicted to cause a serine to proline amino acid substitution at position 352 of the encoded protein (p.S352P).
|Allele Name||Bench to Bassinet Program (B2B/CVDC), mutation 2437 Cecilia Lo|
|Allele Type||Chemically induced (ENU)|
|Gene Symbol and Name||Myh10, myosin, heavy polypeptide 10, non-muscle|
|Strain of Origin||C57BL/6J|
|General Note||Summative Diagnosis:|
Cardiovascular Phenotype: Overriding aorta/double outlet right ventricle (DORV) with ventricular septal defect (VSD) and atrioventricular septal defect (AVSD), ventricular myocardial non-compaction
Noncardiovascular Phenotype: Exencephaly, cleft lip/facial cleft, and micrognathia