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Allele : b2b827Clo Mutant line 827; Bench to Bassinet Program (B2B/CVDC), mutation 827 Cecilia Lo
Primary Identifier  MGI:5317766 Allele Type  Chemically induced (ENU)
Gene  b2b827Clo Strain of Origin  C57BL/6J
Is Recombinase  false Is Wild Type  false
Project Collection  B2B/CvDC
description  Summative Diagnosis:
Cardiac defect phenotype: Left ventricular hypertrophy and perimembranous (pm)/muscular (m) ventricular septal defect (VSD)
Non-cardiovascular defects: Cleft palate, cleft lip, micrognathia, and anophthalmia

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
1300 Ventricular septal defect
3608 Left ventricular hypertrophy
3804 Congenital heart disease
4163 Micrognathia
4401 Cleft palate and cleft lip
4864 Anophthalmia

molecularNote  This ENU-induced mutation was isolated in a screen at the University of Pittsburgh.
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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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