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Tmem79m1J
Spontaneous Allele Detail
Summary
Symbol: Tmem79m1J
Name: transmembrane protein 79; mutation 1, Jackson
MGI ID: MGI:5299918
Gene: Tmem79  Location: Chr3:88236351-88241761 bp, - strand  Genetic Position: Chr3, 38.8 cM, cytoband F1
Alliance: Tmem79m1J page
Tmem79m1J/Tmem79m1J mice on the left and right, showing abnormal coat and hair and irritation around the eyes, with sibling control between them

Show the 3 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  129;FVB-Tg(PTH-cre)4167Slib/J
Mutation
description
Allele Type:    Spontaneous
Mutation:    Single point mutation
 
Mutation detailsThis spontaneous mutation has a G-to-A transition that changes amino acid 214 from glycine to arginine (p.G214R). (J:178673, J:222308)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 3 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Tmem79 Mutation:  23 strains or lines available
References
Original:  J:178673 Karst SY, et al., The first Tmem79 mutant mouse. MGI Direct Data Submission. 2011;
All:  2 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
03/19/2024
MGI 6.23
The Jackson Laboratory