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ENRat
Myo1a - myosin IA
Alias:
BBMI
MIHC
Myh1
Myhl
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Predicted to enable actin filament binding activity and microfilament motor activity. Involved in regulation of protein localization. Located in several cellular components, including brush border; growth cone; and membrane raft. Human ortholog(s) of this gene implicated in autosomal dominant nonsyndromic deafness 48 and sensorineural hearing loss. Orthologous to human MYO1A (myosin IA). [provided by Alliance of Genome Resources, Apr 2022]
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Related Mouse Models
Reference
Myo1a Genetics information (+)
mRatBN7.2
Sequence Homology
Transcripts & Proteins
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Tile View
#
Transcript
Length(nt)
Exon Count
CDS(bp)
Protein
Length(aa)
* This data comes from NCBI.
Gene Expression
Tissue-specific RNA expression
Organ
Abundance
Alphabetical
Cell-specific RNA expression
Organ
Abundance
Alphabetical
Interactions
Acting
Regulation
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Related Mouse Models
Type
Name
MGI
Strain of Origin
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Mutations
References Literature
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