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Allele : b2b2815Clo Mutant line 2815; Bench to Bassinet Program (B2B/CVDC), mutation 2815 Cecilia Lo
Primary Identifier  MGI:5616525 Allele Type  Chemically induced (ENU)
Gene  b2b2815Clo Strain of Origin  C57BL/6J
Is Recombinase  false Is Wild Type  false
Project Collection  B2B/CvDC
description  Summative Diagnosis:
Cardiovascular phenotypes: Overriding aorta and perimembranous ventricular septal defect (pmVSD), ventricular hypertrophy

Noncardiovascular phenotype: Craniofacial defects including short snout, micrognathia, agnathia, anopthalmia, low set ears, and cleft palate, multiplex kidneys

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 Codes Code Description
1310 Ventricular septal defect, membranous
1432 Overriding aortic valve
4163 Micrognathia
4864 Anophthalmia
4876 Cleft palate

molecularNote  This ENU-induced mutation was isolated in a screen at the University of Pittsburgh.
  • mutations:
  • Undefined
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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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Trail: Allele




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