Infantile enterocolitis & monogenic inflammatory bowel disease
Gene: NCF1EnsemblGeneIds (GRCh38): ENSG00000158517
EnsemblGeneIds (GRCh37): ENSG00000158517
OMIM: 608512, Gene2Phenotype
NCF1 is in 4 panels
3 reviews
Ellen McDonagh (Genomics England Curator)
Comment on list classification: Promoted from amber to green due to expert review and curated evidence.Created: 12 Oct 2016, 9:09 a.m.
Neil shah (GOSH)
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Radboud University Medical Center, Nijmegen
- UKGTN
- Expert list
- Phenotypes
-
- Chronic granulomatous disease due to deficiency of NCF-1 233700
- OMIM
- 608512
- Clinvar variants
- Variants in NCF1
- Penetrance
- Complete
- Publications
- Panels with this gene
History Filter Activity
panel promoted to version 1
Ellen McDonagh (Genomics England Curator)14th Oct 2016: panel revised according to expert review, additional curation for evidence level and internal clinical review, and promoted to version 1.
Gene classified by Genomics England curator
Ellen McDonagh (Genomics England Curator)This gene has been classified as Green List (High Evidence).
Set publications
Ellen McDonagh (Genomics England Curator)Publications for NCF1 were set to 16972229; 11133775
Gene classified by Genomics England curator
Ellen McDonagh (Genomics England Curator)This gene has been classified as Green List (High Evidence).
Upload gene information
Sarah Leigh (Genomics England Curator)NCF1 was added to Infantile enterocolitis & monogenic inflammatory bowel diseasepanel. Sources: Radboud University Medical Center, Nijmegen,UKGTN
Set Phenotypes
Sarah Leigh (Genomics England Curator)Phenotypes for gene NCF1 were set to Chronic granulomatous disease due to deficiency of NCF-1 233700
Created
Ellen McDonagh (Genomics England Curator)NCF1 was created by ellenmcdonagh
Added New Source
Ellen McDonagh (Genomics England Curator)NCF1 was added to Infantile enterocolitis & monogenic inflammatory bowel diseasepanel. Sources: Expert list