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Allele : b2b191Clo Mutant line 191; Bench to Bassinet Program (B2B/CVDC), mutation 191 Cecilia Lo
Primary Identifier  MGI:5297421 Allele Type  Chemically induced (ENU)
Gene  b2b191Clo Strain of Origin  C57BL/6J
Is Recombinase  false Is Wild Type  false
Project Collection  B2B/CvDC
description  Summative Diagnosis:
Cardiovascular defects: Double outlet right ventricle (DORV),overriding aorta, ventricular septal defects (VSD), atrio-ventricular septal defects (AVSD), pulmonary stenosis (outflow track and main-pulmonary artery), right aortic arch (RAA), and left coronary artery fistula.
Non-cardiovascular defect: Cleft palate

Fyler Codes
The Fyler code developed by The Boston Children's Heart Foundation in Boston Children's Hospital provides a hierarchical clinical diagnosis of congenital cardiovascular defects and other disorders. These codes are used to delineate pathology in the mutant mouse models that parallel human disease and can be cross referenced to the International Pediatric and Congenital Cardiac Code (IPCCC) (http://www.ipccc.net/).

Fyler Code ID Code Description
0606 DORV + AVSD (AV canal)
1310 Ventricular septal defect, membranous
1320 Ventricular septal defect, muscular
2230 Coronary fistula (arterio-venous or arterio-cameral)
2721 Right aortic arch with abnormal branching pattern
3804 Congenital heart disease

molecularNote  This ENU-induced mutation was isolated in a screen at the University of Pittsburgh.
  • synonyms:
  • Shizou (SHIN-TSO),
  • Shizou (SHIN-TSO)
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

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