Entity Details

Primary name MYO15A
Entity type gene
Source Source Link

Details

PrimaryID51168
RefseqGeneNG_011634
SymbolMYO15A
Namemyosin XVA
Chromosome17
Location17p11.2
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-03-31
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsMYO15_HUMAN

GO terms

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GOName
GO:0000146 microfilament motor activity
GO:0005516 calmodulin binding
GO:0005524 ATP binding
GO:0005737 cytoplasm
GO:0007015 actin filament organization
GO:0007605 sensory perception of sound
GO:0015629 actin cytoskeleton
GO:0016459 myosin complex
GO:0030050 vesicle transport along actin filament
GO:0031982 vesicle
GO:0032420 stereocilium
GO:0051015 actin filament binding
GO:0070062 extracellular exosome
GO:0098858 actin-based cell projection

Diseases

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Disease IDSourceNameDescription
600316 OMIMDeafness, autosomal recessive, 3 (DFNB3)A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. The disease is caused by variants affecting the gene represented in this entry.

Interactions

7 interactions

InteractorPartnerSourcesPublicationsLink
MYO15AEPS8BioGRID, HPRD, IntAct16169070 details
MYO15AUSP13BioGRID, HPRD, IntAct16169070 details
MYO15AFASLGBioGRID, IntAct19807924 details
MYO15AWHRNHPRD15590698 details
MYO15AHSF4BioGRID, IntAct25036637 details
MYO15AAGR2BioGRID30575818 details
MYO15ABRD4BioGRID32416067 details