stereocilin (STRC)

Compartment

• cell surface
• associated with hair bundle

Pathology

• defects in STRC are a cause of autosomal recessive non-syndromic sensorineural deafness type 16

More general terms

• glycoprotein

Database

• OMIM: https://mirror.omim.org/entry/603720
• OMIM: https://mirror.omim.org/entry/606440
• UniProt: http://www.uniprot.org/uniprot/Q7RTU9.html