About   Help   FAQ
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
Loading...
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
12/10/2024
MGI 6.24
The Jackson Laboratory