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b2b2101Clo
Chemically induced Allele Detail
Nomenclature
Symbol: b2b2101Clo
Name: Mutant line 2101; Bench to Bassinet Program (B2B/CVDC), mutation 2101 Cecilia Lo
MGI ID: MGI:5560802
Gene: b2b2101Clo  Location: unknown  
Mutant 2101-005-1 (E15.5) has an interrupted aorta with a RAA and parallel outflow tracts which is diagnosed as DORV by EFIC imaging

Show the 4 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  C57BL/6J
Project Collection: B2B/CvDC
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Undefined
    This ENU-induced mutation was isolated in a screen at the University of Pittsburgh. (J:175213)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 5 anatomical structures
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any b2b2101Clo Mutation:  1 strain or line available
Notes
Summative Diagnosis:
Cardiovascular Phenotype (one mutant): Double outlet right ventricle (DORV) with subaortic ventricular septal defect (VSD), right aortic arch (RAA), interrupted aortic arch (IAA), vascular ring, right atrial isomerism, and dual inferior vena cava (IVC)
Noncardiovascular Phenotype (one mutant): Microphthalmia

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
0600 Double outlet right ventricle
1250 Interrupted aortic arch
1300 Ventricular septal defect
2700 Abnormal aortic arch
2720 Right aortic arch
2760 Vascular ring
2810 Inferior vena cava anomaly
4877 Microphthalmia
4906 Non-cardiac abnormality

References
Original:  J:175213 Lo C, Information submitted by the NHLBI Cardiovascular Development Consortium (CvDC), Bench to Bassinet Program (B2B/CvDC). MGI Direct Data Submission (B2B/CvDC). 2011-15;
All:  2 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
11/23/2021
MGI 6.17
The Jackson Laboratory