Hoxc13^N
Spontaneous Allele Detail

Summary

• Symbol: Hoxc13^N
• Name: homeobox C13; naked
• MGI ID: MGI:1861361
• Gene: Hoxc13 Location: Chr15:102829566-102837249 bp, + strand Genetic Position: Chr15, Syntenic
• Alliance: Hoxc13^N page

Mutation origin

• Strain of Origin: Not Specified

Mutation description

• Allele Type: Spontaneous (Not Specified)
• Mutation: Single point mutation
• Mutation details: A spontaneous mutation produces the point mutation C to A that results in the amino acid substitution of serine to a stop codon at position 298 (S298*). (J:319564)
• Inheritance: Semidominant

Expression

In Structures Affected by this Mutation:

8 anatomical structure(s)

Tumor Data

List all tumor models in MMHCdb carrying Hoxc13^N

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 Hoxc13 Mutation: 15 strains or lines available

Notes

Arose as a spontaneous mutation in a stock at the Latvian University of Riga (J:14939).

References

• Original: J:14939 Lebedinsky NG, et al., Atrichosis und ihre Vererbung bei der albinotischen Hausmaus. Biol Zentralbl. 1927;47:748-52
• All: 12 reference(s)