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  3. SCNN1B
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Familial pulmonary fibrosis

Gene: SCNN1B

Red List (low evidence)
SCNN1B (sodium channel epithelial 1 beta subunit)
EnsemblGeneIds (GRCh38): ENSG00000168447
EnsemblGeneIds (GRCh37): ENSG00000168447
OMIM: 600760, Gene2Phenotype
SCNN1B is in 10 panels

2 reviews

Philip Molyneaux (Imperial College)

Red List (low evidence)

Bronchiectasis rather than fibrosis
Created: 26 Apr 2017, 12:15 p.m.
Created: 26 Apr 2017, 12:15 p.m.

Panel version: 0.110

Alice Gardham (Genomics England)

Comment when marking as ready: Bronchiectasis rather than lung fibrosis-not a relevant phenotype
Created: 8 Feb 2017, 6:01 p.m.
Created: 8 Feb 2017, 6:01 p.m.

Panel version: 0.34

History Filter Activity

27 Apr 2017, Gel status: 1

panel promoted to version 1

Louise Daugherty (Genomics England Curator)

Panel reviews were assessed, and panel was revised according to reviews and further curation. 27th April 2017

8 Feb 2017, Gel status: 1

Gene classified by Genomics England curator

Alice Gardham (Genomics England)

This gene has been classified as Red List (Low Evidence).

29 Oct 2015, Gel status: 0

Created

Ellen McDonagh (Genomics England Curator)

SCNN1B was created by ellenmcdonagh

29 Oct 2015, Gel status: 1

Added New Source

Ellen McDonagh (Genomics England Curator)

SCNN1B was added to Familial pulmonary fibrosispanel. Sources: Emory Genetics Laboratory