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Tmem79ma
Spontaneous Allele Detail
Nomenclature
Symbol: Tmem79ma
Name: transmembrane protein 79; matted
MGI ID: MGI:1856947
Synonyms: ma, matted
Gene: Tmem79  Location: Chr3:88235960-88241740 bp, - strand  Genetic Position: Chr3, 38.8 cM, cytoband F1
Mutation
origin
Strain of Origin:  CBA/CaGr
Mutation
description
Allele Type:    Spontaneous
Mutation:    Single point mutation
 
Mutation detailsA spontaneous C-to-G nonsense mutation results in the substitution of a stop for a tyrosine at position 280 (p.Y280*). (J:202316, J:202453)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 8 anatomical structures
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 2 strains available      Cell Lines: 0 lines available
Carrying any Tmem79 Mutation:  20 strains or lines available
References
Original:  J:24772 Searle AG, et al., Matted (symbol ma). Mouse News Lett. 1954;11:29
All:  14 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
11/30/2021
MGI 6.17
The Jackson Laboratory