Function
Regulates the organization and stability of the microtubule network of sensory neurons to allow axonal transport.
Biological Context
Subcellular Location: Cytoplasm, cytoskeleton; Cytoplasm, cell cortex; Cell membrane (Lipid-anchor)
Tissue Specificity: Isoform 1 is expressed in myoblasts (at protein level). Isoform 3 is expressed in the skin. Isoform 6 is expressed in the brain. Highly expressed in skeletal muscle and cultured keratinocytes
Disease Association: Neuropathy, hereditary sensory and autonomic, 6 (HSAN6) : A form of hereditary sensory and autonomic neuropathy, a genetically and clinically heterogeneous group of disorders characterized by degeneration of dorsal root and autonomic ganglion cells, and by sensory and/or autonomic abnormalities. HSAN6 is a severe autosomal recessive disorder characterized by neonatal hypotonia, respiratory and feeding difficulties, lack of psychomotor development, and autonomic abnormalities including labile cardiovascular function, lack of corneal reflexes leading to corneal scarring, areflexia, and absent axonal flare response after intradermal histamine injection. [The disease is caused by variants affecting the gene represented in this entry] | Epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency (EBS3) : A form of epidermolysis bullosa, a genodermatosis characterized by recurrent blistering, fragility of the skin and mucosal epithelia, and erosions caused by minor mechanical trauma. EBS3 is an autosomal recessive disorder characterized by skin blistering mainly occurring on the feet and ankles. Ultrastructural analysis of skin biopsy shows abnormal hemidesmosomes with poorly formed inner plaques. [The disease is caused by variants affecting the gene represented in this entry]
Product Specifications
Mouse anti-Human sapiens (Human) DST Monoclonal Antibody is a recombinant protein. Suitable for ELISA and Western Blot applications. Explore more Antibody products →
