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Allele : b2b1297Clo Mutant line 1297; Bench to Bassinet Program (B2B/CVDC), mutation 1297 Cecilia Lo
Primary Identifier  MGI:5438057 Allele Type  Chemically induced (ENU)
Gene  b2b1297Clo Strain of Origin  C57BL/6J
Is Recombinase  false Is Wild Type  false
Project Collection  B2B/CvDC
description  Summative Diagnosis:
Cardiovascular phenotype: Double outlet right ventricle (DORV), pulmonary stenosis, thickened semilunar and atrioventircular valves, atrioventricular septal defects (AVSD), ventricular septal defect (VSD)
Noncardiac phenotype: Hepatic cyst

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
0600 Double outlet right ventricle
1300 Ventricular septal defect
1486 Thickened aortic valve cusp(s)
1610 Pulmonary stenosis
2050 Atrial septal defect
4447 Hepatic malformation

molecularNote  This ENU-induced mutation was isolated in a screen at the University of Pittsburgh.
  • synonyms:
  • GCG,
  • GCG
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

2 Carried By

0 Driven By

4 Publication categories





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