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Allele : b2b1163.2Clo Mutant line 1163.2; Bench to Bassinet Program (B2B/CVDC), subline 1163.2 Cecilia Lo
Primary Identifier  MGI:5433410 Allele Type  Chemically induced (ENU)
Gene  b2b1163.2Clo Strain of Origin  C57BL/6J
Is Recombinase  false Is Wild Type  false
Project Collection  B2B/CvDC
description  Summative Diagnosis:
Cardiac defects: Ventricular hypertrophy

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
3608 Left ventricular hypertrophy
3609 Right ventricular hypertrophy

molecularNote  This mutation was derived from the parent line b2b1163Clo.

This ENU-induced mutation was isolated in a screen at the University of Pittsburgh. It is a subline of b2b1163Clo.
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

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Trail: Allele

0 Driven By

3 Publication categories

Trail: Allele




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