WHRN protein, human

Preferred Label : WHRN protein, human;

MeSH note : defects in whirlin, a key component of the stereocilia membrane & a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31; GenBank AB040959; RefSeq XM_027012;

MeSH synonym : Autosomal recessive deafness type 31 protein, human; deafness, autosomal recessive 31 protein, human; whirlin protein, human; DFNB31 protein, human;

Is substance : O;

Details

Origin ID

C477219;

UMLS CUI

C1311555;

MeSH term(s) associated for indexing
- membrane proteins [MeSH Descriptor]
Record concept(s)
- WHRN protein, human [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Biologically Active Substance [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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