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Usher syndrome type-1G protein

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Required for normal development and maintenance of cochlear hair cell bundles. Anchoring/scaffolding protein that is a part of the functional network formed by USH1C, USH1G, CDH23 and MYO7A that mediates mechanotransduction in cochlear hair cells. Required for normal hearing.

Below are the list of possible Usher syndrome type-1G protein products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.
 

Usher syndrome type-1G protein

 Usher syndrome type-1G protein ELISA Kit
 Usher syndrome type-1G protein Recombinant
 Usher syndrome type-1G protein Antibody
Also known as Usher syndrome type-1G protein (Scaffold protein containing ankyrin repeats and SAM domain).
USH1G: Required for normal development and maintenance of cochlear hair cell bundles. Anchoring/scaffolding protein that is a part of the functional network formed by USH1C, USH1G, CDH23 and MYO7A that mediates mechanotransduction in cochlear hair cells. Required for normal hearing. Defect
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s in USH1G are the cause of Usher syndrome type 1G (USH1G). USH is a genetically heterogeneous condition characterized by the association of retinitis pigmentosa and sensorineural deafness. Age at onset and differences in auditory and vestibular function distinguish Usher syndrome type 1 (USH1), Usher syndrome type 2 (USH2) and Usher syndrome type 3 (USH3). USH1 is characterized by profound congenital sensorineural deafness, absent vestibular function and prepubertal onset of progressive retinitis pigmentosa leading to blindness.

Protein type: Cytoskeletal

Chromosomal Location of Human Ortholog: 17q25.1

Cellular Component: actin cytoskeleton

Molecular Function: protein binding; spectrin binding

Biological Process: equilibrioception; photoreceptor cell maintenance; sensory perception of light stimulus; sensory perception of sound

Disease: Usher Syndrome, Type Ig
 USH1G ELISA Kit
 USH1G Recombinant
 USH1G Antibody
 SANS ELISA Kit
 SANS Recombinant
 SANS Antibody
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Usher syndrome type-1G protein homolog

 Usher syndrome type-1G protein homolog ELISA Kit
 Usher syndrome type-1G protein homolog Recombinant
 Usher syndrome type-1G protein homolog Antibody
Also known as Usher syndrome type-1G protein homolog (Jackson shaker protein) (Scaffold protein containing ankyrin repeats and SAM domain).
USH1G: Required for normal development and maintenance of cochlear hair cell bundles. Anchoring/scaffolding protein that is a part of the functional network formed by USH1C, USH1G, CDH23 and MYO7A that mediates mechanotransduction in cochlear hair cells. Re
>>>
quired for normal hearing. Defects in USH1G are the cause of Usher syndrome type 1G (USH1G). USH is a genetically heterogeneous condition characterized by the association of retinitis pigmentosa and sensorineural deafness. Age at onset and differences in auditory and vestibular function distinguish Usher syndrome type 1 (USH1), Usher syndrome type 2 (USH2) and Usher syndrome type 3 (USH3). USH1 is characterized by profound congenital sensorineural deafness, absent vestibular function and prepubertal onset of progressive retinitis pigmentosa leading to blindness.

Protein type: Cytoskeletal

Cellular Component: actin cytoskeleton; cytoplasm; membrane; photoreceptor connecting cilium; photoreceptor inner segment

Molecular Function: protein binding; protein homodimerization activity; spectrin binding

Biological Process: equilibrioception; inner ear morphogenesis; inner ear receptor cell differentiation; inner ear receptor stereocilium organization and biogenesis; photoreceptor cell maintenance; sensory perception of light stimulus; sensory perception of sound
 Ush1g ELISA Kit
 Ush1g Recombinant
 Ush1g Antibody
 Sans ELISA Kit
 Sans Recombinant
 Sans Antibody
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