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| Nomenclature |
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Symbol:
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b2b1200.1Clo
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Name:
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Mutant line 1200.1;
Bench to Bassinet Program (B2B/CVDC), mutation 1200, subline 1 Cecilia Lo
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MGI ID: |
MGI:5437102 |
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Gene:
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b2b1200.1Clo
Location:
unknown
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Mutant 1200-003-NA shows dextroversion {S,D,S} with vascular ring
Show the 23 image(s) involving this allele.
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Mutation
origin |
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Strain of Origin:
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C57BL/6J
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Mutation
description |
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Allele
Type: | |
Chemically induced (ENU) |
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Mutation: | |
Undefined |
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Mutation details: This ENU-induced mutation was isolated in a screen at the University of Pittsburgh. It is a subline of b2b1200Clo. (J:175213)
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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Disease models
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available |
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Carrying any b2b1200.1Clo Mutation:
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0 strains or lines available |
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Notes |
Summative Diagnosis:
Mutant Type 1:
Cardiovascular defects: Heterotaxy with congenital heart disease such as dextroversion with hypoplastic right ventricle (RV), double outlet right ventricle (DORV), muscular and membranous ventricular septal defects, aortic arch anomalies including vascular ring
Non-cardiovascular defects: Duplex kidneys with cysts and hydronephrosis
Phenotypic Similarity to Human Syndrome: Heterotaxy, Kartagener's syndrome, Primary ciliary dyskinesia, Polycystic kidney disease
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Analysis Tools
