Summary | Mutation origin | Mutation description | Expression | Phenotypes | Tumor data | Find Mice (IMSR) | Notes | References

Symbol:	Hoxc13N
Name:	homeobox C13; naked
MGI ID:	MGI:1861361
Gene:	Hoxc13  Location: Chr15:102829566-102837249 bp, + strand  Genetic Position: Chr15, Syntenic
Alliance:	Hoxc13N page

Strain of Origin:

Not Specified

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

View phenotypes and curated references for all genotypes (concatenated display).

In Structures Affected by this Mutation:

8 anatomical structure(s)

List all tumor models in MMHCdb carrying Hoxc13N

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

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)