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vsd
Chemically induced Allele Detail
Nomenclature
Symbol: vsd
Name: ventricular septal defect
MGI ID: MGI:3522333
Synonyms: family 166, hlb546
Gene: vsd  Location: Chr4:39452126-56769494 bp  Genetic Position: Chr4, Syntenic
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Chemically induced (ENU)
Inheritance:    Not Specified
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 6 anatomical structures
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any vsd Mutation:  0 strains or lines available
References
Original:  J:94456 Yu Q, et al., ENU induced mutations causing congenital cardiovascular anomalies. Development. 2004 Dec;131(24):6211-23
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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last database update
05/15/2018
MGI 6.12
The Jackson Laboratory