MeSH Browser

MeSH Supplementary: CLC-1 channel
Unique ID: C086321
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C086321
Entry Term(s): CIC-1 protein, human; CLC-1 protein, human; CLC-1 protein, mouse; CLC-1 protein, rat; CLCN1 protein, human; Clcn1 protein, mouse; Clcn1 protein, rat; chloride channel 1 protein, mouse; chloride channel 1 protein, rat; chloride channel 1, skeletal muscle (Thomsen disease, autosomal dominant), human; skeletal muscle chloride channel CIC-1; skeletal muscle chloride channel CIC-1, human
Previous Indexing: *MUSCLE PROTEINS (94-99)
Heading Mapped to: *Chloride Channels
Frequency: 312
Note: the major skeletal muscle chloride channel in mammals; CLCN1 mutations are associated with myotonia congenita in Northern Scandinavia; RefSeq NM_000083 (human); NM_013491 (mouse); NM_013147 (rat)
Source: Biophys J 1994 Jan;66(1):149-52
Indexing Information: Myotonia Congenita
Date of Entry: 1994/04/15
Revision Date: 2005/12/19

CLC-1 channel MeSH Supplementary Concept Data 2024