Usher Syndrome Type-1G Protein

**Semantic type:** Amino Acid, Peptide, or Protein

**Definition:** Usher syndrome type-1G protein (461 aa, ~51 kDa) is encoded by the human USH1G gene. This protein plays a role in retinal and cochlear development.

**Synonyms:** - Scaffold Protein Containing Ankyrin Repeats and SAM Domain - USH1G