Entity Details

Primary name MYO3A
Entity type gene
Source Source Link

Details

PrimaryID53904
RefseqGeneNG_011635
SymbolMYO3A
Namemyosin IIIA
Chromosome10
Location10p12.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2000-05-24
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsMYO3A_HUMAN

GO terms

Show/Hide Table
GOName
GO:0000146 microfilament motor activity
GO:0003779 actin binding
GO:0004672 protein kinase activity
GO:0005516 calmodulin binding
GO:0005524 ATP binding
GO:0005737 cytoplasm
GO:0007601 visual perception
GO:0007605 sensory perception of sound
GO:0016459 myosin complex
GO:0030175 filopodium
GO:0031941 filamentous actin
GO:0032426 stereocilium tip
GO:0032433 filopodium tip
GO:0043531 ADP binding
GO:0046777 protein autophosphorylation
GO:0050896 response to stimulus
GO:0060002 plus-end directed microfilament motor activity
GO:0090103 cochlea morphogenesis
GO:0106310 protein serine kinase activity
GO:0106311 protein threonine kinase activity

Diseases

Show/Hide Table
Disease IDSourceNameDescription
607101 OMIMDeafness, autosomal recessive, 30 (DFNB30)A form of non-syndromic deafness characterized by bilateral progressive hearing loss, which first affects the high frequencies. Hearing loss begins in the second decade, and by age 50 is severe in high and middle frequencies and moderate at low frequencies. The disease is caused by variants affecting the gene represented in this entry.

Interactions

8 interactions