MYO5A
Sign in to saveAlso known as MYR12, GS1, MYH12, MYO5, myosin VA
protein-coding gene in the species Homo sapiens
Gene data
MYO5A- Name
- myosin VA
- Type
- protein-coding
- Aliases
- GS1, MYH12, MYO5, MYR12
This gene is one of three myosin V heavy-chain genes, belonging to the myosin gene superfamily. Myosin V is a class of actin-based motor proteins involved in cytoplasmic vesicle transport and anchorage, spindle-pole alignment and mRNA translocation. The protein encoded by this gene is abundant in melanocytes and nerve cells. Mutations in this gene cause Griscelli syndrome type-1 (GS1) and neuroectodermal melanolysosomal disease, or Elejalde disease. [provided by RefSeq, Sep 2023].
via MyGene.info
Gene · Ensembl
myosin VA
- Symbol
- MYO5A
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 15:52,307,281-52,529,248
- Strand
- Reverse (−)
- Assembly
- GRCh38
View on Ensembl →
via Ensembl · EMBL-EBI