USH1C Products

Description

USH1C may be involved in protein-protein interaction. Defects in USH1C are the cause of Usher syndrome type 1c. It is an autosomal recessive sensory defect involving congenital profound sensorineural deafness, vestibular dysfunction, and blindness due to progressive retinitis pigmentosa. Defects in USH1C are also the cause of nonsyndromic recessive deafness.

Bioinformatics

Entrez	10083 Human 308596 Rat 72088 Mouse
Uniprot	AAH16057 Human AAH16057.1 Human NP_005700. Human NP_005700.2 Human NP_710142 Human Q9Y6N9 Human
Product By Gene ID	10083
Alternate Names	AIE75 AIE-75 Antigen NY-CO-38/NY-CO-37 Autoimmune enteropathy-related antigen AIE-75 deafness, autosomal recessive 18 DFNB18 harmonin NY-CO-37 NY-CO-38 PDZ-45 PDZ73 PDZ-73 PDZ-73/NY-CO-38 Protein PDZ-73 Renal carcinoma antigen NY-REN-3 ush1cpst Usher syndrome 1C (autosomal recessive, severe) Usher syndrome type-1C protein

Research Areas for USH1C

Find related products by research area and learn more about each of the different research areas below.

Signal Transduction
Vision

Related USH1C Blog Posts

Check out the latest blog posts on USH1C.

Auditory Infographic: Can you hear me now? The auditory process involves several structures of the ear to convert sound waves into information that is processed by our brain. Learn more about the auditory process in our infographic below. Novus Biologicals offers reagents mentioned in the inf...    Read more.

Read more USH1C related blogs.