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Allele : b2b904Clo Mutant line 904; Bench to Bassinet Program (B2B/CVDC), mutation 904 Cecilia Lo
Primary Identifier  MGI:5431494 Allele Type  Chemically induced (ENU)
Gene  b2b904Clo Strain of Origin  C57BL/6J
Is Recombinase  false Is Wild Type  false
Project Collection  B2B/CvDC
description  Summative Diagnosis:
Mutant phenotype 1: Right ventricular myocardial noncompaction, dilated ventricular chamber
Mutant phenotype 2: Biventricular 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
1802 Excessive myocardial trabeculation or noncompaction
3608 Left ventricular hypertrophy
3609 Right ventricular hypertrophy
7505 Biventricular hypertrophy

molecularNote  This ENU-induced mutation was isolated in a screen at the University of Pittsburgh. More than one mutation in this line results in a discernible phenotype in a homozygous recessive screen. At least two segregating phenotype groups are identified. See b2b904.1Clo and b2b904.2Clo
  • synonyms:
  • Bright Eyes,
  • Bright Eyes
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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

3 Publication categories





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