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lgSt
Spontaneous Allele Detail
Summary
Symbol: lgSt
Name: lid gap; lid gap Strong
MGI ID: MGI:1857110
Gene: lg  Location: Chr13:110699804-112898424 bp  Genetic Position: Chr13, Syntenic
Alliance: lgSt page
Mutation
origin
Strain of Origin:  L
Mutation
description
Allele Type:    Spontaneous
Mutation:    Undefined
    This allele was identified from the results of noncomplementation tests with lg and lgMl. (J:5056)
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 lg Mutation:  0 strains or lines available
Notes
This allele is believed to be extinct.
References
Original:  J:27504 Strong LC, The inheritance of cataract and allied eye defects in the house mouse. Proc Sixth Int Cong Genet. 1932;2:195 (Abstr.)
All:  7 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