Mc1r^E-so
Spontaneous Allele Detail

Summary

• Symbol: Mc1r^E-so
• Name: melanocortin 1 receptor; sombre
• MGI ID: MGI:1856029
• Synonyms: E^so, So
• Gene: Mc1r Location: Chr8:124133846-124137483 bp, + strand Genetic Position: Chr8, 72.1 cM
• Alliance: Mc1r^E-so page

Mutation origin

• Strain of Origin: C3H

Mutation description

• Allele Type: Spontaneous
• Mutation: Single point mutation
• Mutation details: A T-to-C mutation in codon 98 is predicted to result in a leucine to proline alteration at this position (p.L98P). (J:4636)
• Inheritance: Semidominant

Expression

In Structures Affected by this Mutation:

1 anatomical structure(s)

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 4 strains available Cell Lines: 0 lines available
• Carrying any Mc1r Mutation: 43 strains or lines available

References

• Original: J:13077 Bateman N, Sombre, a viable dominant mutant in the house mouse. J Hered. 1961;52(4):186-189
• All: 6 reference(s)