Tmem79^m1J
Spontaneous Allele Detail

Summary

• Symbol: Tmem79^m1J
• 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: Tmem79^m1J page

Tmem79^m1J/Tmem79^m1J 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 details: This 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

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: 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)