Familial pulmonary fibrosis
Gene: CCDC40EnsemblGeneIds (GRCh38): ENSG00000141519
EnsemblGeneIds (GRCh37): ENSG00000141519
OMIM: 613799, Gene2Phenotype
CCDC40 is in 12 panels
2 reviews
Philip Molyneaux (Imperial College)
PCD not fibrosis
Created: 26 Apr 2017, 9:50 a.m.
Alice Gardham (Genomics England)
Comment when marking as ready: Primary ciliary dyskinesia (bronchiectasis) rather than fibrosis -not relevant phenotypeCreated: 8 Feb 2017, 5:51 p.m.
Details
- Sources
-
- Expert Review Red
- Emory Genetics Laboratory
- Phenotypes
-
- Ciliary dyskinesia, primary, 15
- OMIM
- 613799
- Clinvar variants
- Variants in CCDC40
- Penetrance
- Complete
- Panels with this gene
-
- Laterality disorders and isomerism
- Non-CF bronchiectasis
- Respiratory ciliopathies including non-CF bronchiectasis
- Ductal plate malformation
- DDG2P
- Familial pulmonary fibrosis
- Skeletal dysplasia
- Fetal anomalies
- Thoracic dystrophies
- Primary ciliary disorders
- Rare multisystem ciliopathy disorders
- Intellectual disability
History Filter Activity
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
Set Phenotypes
Louise Daugherty (Genomics England Curator)Phenotypes for CCDC40 were set to Ciliary dyskinesia, primary, 15
Gene classified by Genomics England curator
Alice Gardham (Genomics England)This gene has been classified as Red List (Low Evidence).
Added New Source
Ellen McDonagh (Genomics England Curator)CCDC40 was added to Familial pulmonary fibrosispanel. Sources: Emory Genetics Laboratory
Created
Ellen McDonagh (Genomics England Curator)CCDC40 was created by ellenmcdonagh