MYO6 Products

Description

MYO6 encodes a protein involved intracellular vesicle and organelle transport, especially in the hair cell of the inner ear. Mutations in this gene have been found in patients with non-syndromic autosomal dominant and recessive hearing loss. [provided by RefSeq]

Bioinformatics

Uniprot	NM_004999 Human
Product By Gene ID	4646
Alternate Names	myosin-VI DFNA22 Unconventional myosin-6 KIAA0389deafness, autosomal recessive 37 DFNB37 myosin VI

Diseases related to MYO6

Discover more about diseases related to MYO6.

Complete Hearing Loss
Sensorineural Hearing Loss (disorder)
Carcinoma
Malignant Neoplasms
Prostatic Neoplasms
Deafness Congenital
Malignant Neoplasm Of Prostate
Fibrosis
Malignant Paraganglionic Neoplasm
Circling Gait
Post-traumatic Stress Disorder
Usher Syndrome
Cardiomyopathies
Malnutrition
Embryonal Carcinoma
Malignant Tumor Of Colon
Tumor Angiogenesis
Neoplasms
Diarrhea

Pathways for MYO6

View related products by pathway and learn more about each of the pathways below.

Endocytosis
Transport
Clathrin-mediated Endocytosis
Localization
Secretion
Synapse Maturation
Golgi Localization
Anion Transport
Ion Transport
Neurogenesis
Synaptic Transmission
Inner Ear Development
Organ Development
Ear Development
Cell Differentiation
Angiogenesis
Hair Cell Differentiation
Pathogenesis
Sensory Organ Development
Exocytosis

PTMs for MYO6

Learn more about PTMs related to MYO6.

Biotinylation

Bioinformatics Tool for MYO6

Discover related pathways, diseases and genes to MYO6. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.