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Allele : b2b997Clo Mutant line 997; Bench to Bassinet Program (B2B/CVDC), mutation 997 Cecilia Lo
Primary Identifier  MGI:5311380 Allele Type  Chemically induced (ENU)
Gene  b2b997Clo Strain of Origin  C57BL/6J
Is Recombinase  false Is Wild Type  false
Project Collection  B2B/CvDC
description  Summative Diagnosis:
Cardiovascular defects: Heterotaxy with right pulmonary isomerism and congenital heart disease including transposition of the great arteries (TGA), double outlet right ventricle (DORV), and atrio-ventricular septal defects (AVSD)

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
0190 Heterotaxy syndrome
0606 DORV + AVSD (AV canal)
0700 D-loop transposition of the great arteries
1132 Unbalanced complete common atrioventricular canal
1140 Common atrium
3804 Congenital heart disease
3817 Abdominal situs ambiguous (abdominal heterotaxy)
3950 {S,D,D}
3983 {A,D,D}
4235 Pulmonary malformation

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




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