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Lystbg-grey
Chemically induced Allele Detail
Summary
Symbol: Lystbg-grey
Name: lysosomal trafficking regulator; beige grey
MGI ID: MGI:3620573
Gene: Lyst  Location: Chr13:13764982-13953388 bp, + strand  Genetic Position: Chr13, 5.28 cM
Alliance: Lystbg-grey page
Morphologic investigation of Lystbg-grey/Lystbg-grey and +/+ wild-type mice.

Show the 1 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  C57BL/6
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Nucleotide substitutions
 
Mutation detailsA point mutation of the splice donor site of the intron between exon 25 and exon 26 caused skipping of exon 25 during RNA splicing without disrupting the reading frame. The resulting transcript has a 77 residue deletion. (J:106442)
Inheritance:    Recessive
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: 9 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 Lyst Mutation:  225 strains or lines available
References
Original:  J:106442 Runkel F, et al., Grey, a novel mutation in the murine Lyst gene, causes the beige phenotype by skipping of exon 25. Mamm Genome. 2006 Mar;17(3):203-10
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
04/16/2024
MGI 6.23
The Jackson Laboratory