DPP6

dipeptidyl peptidase like 6
OMIM: 126141, Gene2Phenotype

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Red DPP6 in Idiopathic ventricular fibrillation Level 3: Cardiac arrhythmia Level 2: Cardiovascular disorders Version 1.2	review	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Red Radboud University Medical Center, Nijmegen Phenotypes Ventricular fibrillation, paroxysmal familial, 2,
Red DPP6 in Autism Version 0.36	review	Not set	Sources Expert Review Red SFARI
Amber DPP6 in Severe microcephaly Level 3: DNA repair disorders Level 2: Dysmorphic and congenital abnormality syndromes Version 5.7 Latest signed off version: v5.0 (1 May 2024)	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber NHS GMS Expert list Phenotypes Intellectual developmental disorder, autosomal dominant 33, OMIM:616311 Tags deletions
Red DPP6 in Intellectual disability Level 3: Neurodevelopmental disorders Level 2: Neurology and neurodevelopmental disorders Version 6.11 Latest signed off version: v6.0 (1 May 2024) Component of the following Super Panels: Childhood onset leukodystrophy Hypotonic infant Paediatric disorders	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources NHS GMS Expert Review Red Other Phenotypes Intellectual developmental disorder, autosomal dominant 33, OMIM:616311 Tags deletions
Green DPP6 in Severe Paediatric Disorders Version 1.184	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Next Generation Children Project Expert Review Green Expert list Phenotypes Mental retardation, autosomal dominant 33, 616311