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Allele : Lhfpl5<hscy> lipoma HMGIC fusion partner-like 5; hurry-scurry

Primary Identifier  MGI:3055797 Allele Type  Spontaneous
Attribute String  Null/knockout Gene  Lhfpl5
Inheritance Mode  Recessive Strain of Origin  B6.MOR-Gusb<a>
Is Recombinase  false Is Wild Type  false
molecularNote  This spontaneous mutation arose at The Jackson Laboratory. The mutation is a G-to-T transversion in exon 2 that results in a nonconservative amino acid change from cysteine to phenylalanine at amino acid position 161 of the encoded protein (p.C161F). Northern blot analysis demonstrated that a normal sized transcript was expressed from this mutant allele. Histological immunofluorescence analysis confirmed the absence of protein expression in newborn homozygous mice that is normally found in the inner and outer hair cells of the inner ear.
  • mutations:
  • Single point mutation
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

0 Driven By

4 Publication categories