Cystic Fibrosis Transmembrane Conductance Regulator
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)
Year introduced: 1996
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Subheadings:
Tree Number(s): D12.776.157.530.100.304.500, D12.776.157.530.400.175.125, D12.776.157.530.450.074.500.500.500.500, D12.776.543.550.450.175.125, D12.776.543.585.100.304.500, D12.776.543.585.400.175.125, D12.776.543.585.450.074.500.500.500.500
MeSH Unique ID: D019005
Registry Number: 126880-72-6
Entry Terms:
- Chloride channels, ATP-gated CFTR
- Chloride channels, ATP gated CFTR
- CFTR Protein
- Protein, CFTR
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