Hu, Mu, RtApplications:
WB, ICC/IF, IHC, IHC-PHost:
Applications: WB, ELISA, IHC, IHC-P, IP
Host: Rabbit Polyclonal
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.
|Product By Gene ID
- Protein PDZ-73
- Autoimmune enteropathy-related antigen AIE-75
- Antigen NY-CO-38/NY-CO-37
- deafness, autosomal recessive 18
- Usher syndrome type-1C protein
- Renal carcinoma antigen NY-REN-3
- Usher syndrome 1C (autosomal recessive, severe)
Research Areas for USH1C
Find related products by research area and learn more about each of the different research areas below.Signal TransductionVision
Bioinformatics Tool for USH1C
Discover related pathways, diseases and genes to USH1C. Need help? Read the Bioinformatics Tool Guide
for instructions on using this tool.
Related USH1C Blog Posts
Check out the latest blog posts on USH1C.
Read more USH1C related blogs.
|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.