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Allele : Myo1d<m1Btlr> myosin ID; mutation 1, Bruce Beutler

Primary Identifier  MGI:6268405 Allele Type  Chemically induced (ENU)
Attribute String  Hypomorph Gene  Myo1d
Inheritance Mode  Recessive Strain of Origin  C57BL/6J
Is Recombinase  false Is Wild Type  false
Project Collection  Beutler Mutagenetix
molecularNote  ENU-induced A to T transversion at base pair 80,674,708 (v38) on chromosome 11, or base pair 105,348 in the GenBank genomic region NC_000077 encoding Myo1d. The mutation corresponds to residue 1,435 in the mRNA sequence NM_177390 within exon 10 of 22 total exons. The mutation results in an asparagine (N) to isoleucine (I) substitution at amino acid 401 in the Myo1d protein.
  • mutations:
  • Single point mutation
  • synonyms:
  • horton,
  • horton,
  • Myo1d<htn>,
  • horton,
  • Myo1d<htn>
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

3 Carried By

0 Driven By

3 Publication categories