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Allele : Mc1r<e> melanocortin 1 receptor; recessive yellow
Primary Identifier  MGI:1856028 Allele Type  Spontaneous
Gene  Mc1r Inheritance Mode  Recessive
Strain of Origin  C57BL/6Ha Is Recombinase  false
Is Wild Type  false
molecularNote  The mutation is a frameshift due to a deletion of a single nucleotide at position 549. This mutation is predicted to result in a protein that continues out of frame for 12 amino acids before terminating.
  • mutations:
  • Intragenic deletion
  • synonyms:
  • e,
  • Mc1r<->,
  • e,
  • MC1<->,
  • MC1<->,
  • Mc1r<->
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

8 Carried By

0 Driven By

46 Publication categories





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