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Hspa5baffled
Chemically induced Allele Detail
Summary
Symbol: Hspa5baffled
Name: heat shock protein 5; baffled
MGI ID: MGI:4888745
Synonyms: ND58
Gene: Hspa5  Location: Chr2:34662102-34666541 bp, + strand  Genetic Position: Chr2, 22.94 cM
Alliance: Hspa5baffled page
Mutation
origin
Strain of Origin:  BALB/c x C57BL/6
Mutation
description
Allele Type:    Chemically induced (ENU) (Hypomorph)
Mutation:    Single point mutation
 
Mutation detailsENU induced an A to G transition in exon 1 that results in the amino acid substitution of glycine for glutamic acid at position 26 (E26G). This mutation alters a conserved hydrophilic motif that forms the N-terminus after the signal peptidase cleavage. Expression level and localization are not disrupted. This allele is hypomorphic. (J:191772)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 15 anatomical structure(s)
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 Hspa5 Mutation:  38 strains or lines available
Notes
Originally generated from male mice expressing Tg(Mbp-MAPT/lacZ)#Caw.
References
Original:  J:168258 Dwyer ND, et al., A forward genetic screen with a thalamocortical axon reporter mouse yields novel neurodevelopment mutants and a distinct emx2 mutant phenotype. Neural Dev. 2011;6:3
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
04/23/2024
MGI 6.23
The Jackson Laboratory