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Sptbn4qv-2J
Spontaneous Allele Detail
Summary
Symbol: Sptbn4qv-2J
Name: spectrin beta, non-erythrocytic 4; quivering 2 Jackson
MGI ID: MGI:1856540
Gene: Sptbn4  Location: Chr7:27055808-27147111 bp, - strand  Genetic Position: Chr7, 15.88 cM, cytoband A3
Alliance: Sptbn4qv-2J page
Mutation
origin
Strain of Origin:  CXB6/ByJ
Mutation
description
Allele Type:    Spontaneous
Mutation:    Intragenic deletion
 
Mutation detailsThe mutation is a 7 bp deletion of coding nucleotides 5185-5191 (transcript XM_006540436) that causes a frameshift at arginine 1729. (J:71549)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references 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: 0 strains available      Cell Lines: 0 lines available
Carrying any Sptbn4 Mutation:  122 strains or lines available
Notes
Extinct.
References
Original:  J:14995 Rauch SD, Hereditary deafness of central origin in two new alleles of the quivering mutation. Mouse News Lett. 1987;78:44
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
12/10/2024
MGI 6.24
The Jackson Laboratory