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Cacnb4lh
Spontaneous Allele Detail
Summary
Symbol: Cacnb4lh
Name: calcium channel, voltage-dependent, beta 4 subunit; lethargic
MGI ID: MGI:1856936
Synonyms: beta4lh, lh
Gene: Cacnb4  Location: Chr2:52318332-52566816 bp, - strand  Genetic Position: Chr2, 29.98 cM
Alliance: Cacnb4lh page
Mutation
origin
Strain of Origin:  BALB/cGn
Mutation
description
Allele Type:    Spontaneous
Mutation:    Insertion
 
Mutation detailsA four bp insertion that disrupts the consensus 5' splice site of intron A/B was identified. Reduced levels of transcripts are produced from this allele and are present at approximately 20% of the normal levels in homozygous mice. (J:38214)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 2 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation: 11 anatomical structure(s)
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 Cacnb4 Mutation:  32 strains or lines available
References
Original:  J:28465 Dickie MM, Lethargic (lh). Mouse News Lett. 1964;30:31
All:  34 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
04/16/2024
MGI 6.23
The Jackson Laboratory