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Chemically induced Allele Detail
Symbol: b2b1584Clo
Name: Mutant line 1584; Bench to Bassinet Program (B2B/CVDC), mutation 1584 Cecilia Lo
MGI ID: MGI:5431501
Synonyms: Nebulous
Gene: b2b1584Clo  Location: unknown  
Mutant 1584-004-LA displays heterotaxy indicated by dextrocardia, abnormal lung lobation and dextrogastria

Show the 12 phenotype image(s) involving this allele.

Strain of Origin:  C57BL/6J
Project Collection: B2B/CvDC
Allele Type:    Chemically induced (ENU)
Mutation:    Undefined
    This ENU-induced mutation was isolated in a screen at the University of Pittsburgh. Additional incidental mutations were detected in sequencing for the causative mutation, b2b1584Clo, and may be present in stocks carrying this mutation.
View phenotypes for all genotypes (concatenated display).
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 b2b1584Clo Mutation:  1 strain or line available
Summative Diagnosis:
Laterality defects including situs inversus totalis and heterotaxia with congenital heart disease: dextrocardia, double outlet right ventricle (DORV), possible crisscross heart, and bilateral inferior vena cavae (IVC)
Noncardiac phenotype: Slow and dyskinetic airway ciliary motion

Phenotypic Similarity to Human Syndrome: Kartagener's Syndrome, Primary Ciliary Dyskinesia, Heterotaxy

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
0181 Crisscross Atrioventricular Valves
0100 Situs inversus totalis
0100 Dextrocardia
0190 Heterotaxy Syndrome
2810 Inferior vena cava anomaly
3804 Congenital heart disease
0600 Double outlet right ventricle

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:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 5.22
The Jackson Laboratory