Infantile enterocolitis & monogenic inflammatory bowel diseaseGene: NCF2
Associated with phenotype in OMIM, not in G2P / DD. Present on UKGTN Very Early Onset Inflammatory Bowel Disease 40 Gene Panel and Emory Genetics Laboratory Early Onset Inflammatory Bowel Disease: Sequencing Panel. Numerous variants reported
Created: 5 Sep 2016, 8:05 a.m.
14th Oct 2016: panel revised according to expert review, additional curation for evidence level and internal clinical review, and promoted to version 1.
NCF2 was added to Infantile enterocolitis & monogenic inflammatory bowel diseasepanel. Sources: Emory Genetics Laboratory,Illumina TruGenome Clinical Sequencing Services,Radboud University Medical Center, Nijmegen,UKGTN
Phenotypes for gene NCF2 were set to Chronic granulomatous disease due to deficiency of NCF-2 233710
NCF2 was created by ellenmcdonagh
NCF2 was added to Infantile enterocolitis & monogenic inflammatory bowel diseasepanel. Sources: Expert list