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Protein Coding Gene : Myo1a myosin IA
Primary Identifier  MGI:107732 Organism  mouse, laboratory
Chromosome  10 NCBI Gene Number  432516
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Enables actin filament binding activity. Acts upstream of or within microvillus assembly. Located in several cellular components, including basal plasma membrane; brush border; and lateral plasma membrane. Is expressed in several structures, including inner ear and intestine. Human ortholog(s) of this gene implicated in sensorineural hearing loss. Orthologous to human MYO1A (myosin IA).
PHENOTYPE: Homozygous null mice display abnormal small intestine brush border morphology, but have normal hearing. [provided by MGI curators]
  • synonyms:
  • MGI:1338019,
  • Myo1a,
  • myosin IA,
  • BBM-I,
  • myosin, heavy polypeptide-like (110kD),
  • Myhl,
  • brush border myosin 1,
  • MGD-MRK-36308
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Trail: ProteinCodingGene




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