Cystic Fibrosis Transmembrane Conductance Regulator D019005

Related MeSH Hierarchy (7)

Chemicals and Drugs [D] » Amino Acids, Peptides, and Proteins [D12] » Proteins » Carrier Proteins » Membrane Transport Proteins » ATP-Binding Cassette Transporters » Multidrug Resistance-Associated Proteins » Cystic Fibrosis Transmembrane Conductance Regulator

Chemicals and Drugs [D] » Amino Acids, Peptides, and Proteins [D12] » Proteins » Carrier Proteins » Membrane Transport Proteins » Ion Channels » Chloride Channels » Cystic Fibrosis Transmembrane Conductance Regulator

Chemicals and Drugs [D] » Amino Acids, Peptides, and Proteins [D12] » Proteins » Membrane Proteins » Membrane Glycoproteins » Ion Channels » Chloride Channels » Cystic Fibrosis Transmembrane Conductance Regulator

Chemicals and Drugs [D] » Amino Acids, Peptides, and Proteins [D12] » Proteins » Membrane Proteins » Membrane Transport Proteins » ATP-Binding Cassette Transporters » Multidrug Resistance-Associated Proteins » Cystic Fibrosis Transmembrane Conductance Regulator

Chemicals and Drugs [D] » Amino Acids, Peptides, and Proteins [D12] » Proteins » Membrane Proteins » Membrane Transport Proteins » Ion Channels » Chloride Channels » Cystic Fibrosis Transmembrane Conductance Regulator

Description

A chloride channel that regulates secretion in many exocrine tissues. Abnormalities in the CFTR gene have been shown to cause cystic fibrosis. (Hum Genet 1994;93(4):364-8)   MeSH

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