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lgMl
Spontaneous Allele Detail
Summary
Symbol: lgMl
Name: lid gap; lid gap Miller
MGI ID: MGI:1857108
Synonyms: lidgap-Miller
Gene: lg  Location: Chr13:110699804-112898424 bp  Genetic Position: Chr13, Syntenic
Alliance: lgMl page
Mutation
origin
Strain of Origin:  C3H/Ml
Mutation
description
Allele Type:    Spontaneous
Mutation:    Undefined
    This allele was identified from the results of noncomplementation tests with lg and lgSt. (J:5056)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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
References
Original:  J:24765 WATNEY MJ, et al., PREVENTION OF A GENETICALLY DETERMINED CONGENITAL EYE ANOMALY IN THE MOUSE BY THE ADMINISTRATION OF CORTISONE DURING PREGNANCY. Nature. 1964 Jun 6;202:1029-31
All:  6 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