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Psma5m1Btlr
Chemically induced Allele Detail
Summary
Symbol: Psma5m1Btlr
Name: proteasome subunit alpha 5; mutation 1, Bruce Beutler
MGI ID: MGI:6725089
Synonyms: Psma5V146G
Gene: Psma5  Location: Chr3:108164242-108187268 bp, + strand  Genetic Position: Chr3, 46.89 cM
Alliance: Psma5m1Btlr page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Chemically induced (ENU) (Not Specified)
Mutation:    Single point mutation
 
Mutation detailsENU mutagenesis produced a T to G point mutation that results in the amino acid substitution of valine with glycine at position 146 (V146G). (J:307652)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 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 Psma5 Mutation:  18 strains or lines available
References
Original:  J:307652 Rios JJ, et al., Saturation mutagenesis defines novel mouse models of severe spine deformity. Dis Model Mech. 2021 Jun 1;14(6):dmm048901
All:  1 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