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Allele : Fbn2<fp> fibrillin 2; fused phalanges

Primary Identifier  MGI:1935123 Allele Type  Spontaneous
Gene  Fbn2 Inheritance Mode  Recessive
Strain of Origin  C3HeB/FeHu Is Recombinase  false
Is Wild Type  false
molecularNote  This mutation consists of a single nucleotide deletion in exon 39 in the Fbn2 gene, causing a frameshift of 44 amino acids before the introduction of a stop codon. RT-PCR analysis revealed that less Fbn2 transcript is produced in the fused phalanges mouse than in the parental strain from which it arose.
  • mutations:
  • Intragenic deletion
  • synonyms:
  • sy<fp>,
  • fp,
  • fp,
  • sy<fp>
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

2 Carried By

0 Driven By

7 Publication categories