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gp
Spontaneous Allele Detail
Summary
Symbol: gp
Name: gaping lids
MGI ID: MGI:1856887
Gene: gp  Location: unknown  Genetic Position: Chr11, Syntenic
Alliance: gp page
Eyelid phenotype, scanning electron micrographs and histological cross-section of E16-E18 gp/gp and normal fetuses.

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

Mutation
origin
Strain of Origin:  C57BL/6-Usp14ax-J
Mutation
description
Allele Type:    Spontaneous
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 4 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 gp Mutation:  0 strains or lines available
References
Original:  J:211 Kelton DE, et al., Gaping, a new open eyelid mutation in the house mouse. Genetics. 1964;50(2):261-2 (Abstr.)
All:  4 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