MPIG6B

megakaryocyte and platelet inhibitory receptor G6b
OMIM: 606520, Gene2Phenotype

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green MPIG6B in Inherited bleeding disorders Level 3: Haemostasis disorders Level 2: Haematological and immunological disorders Version 1.178	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Other Phenotypes Platelet disorder Thrombocytopenia, anemia, and myelofibrosis
Red MPIG6B in Cytopenias and congenital anaemias Level 3: Anaemias and red cell disorders Level 2: Haematological disorders Version 1.118	review	BIALLELIC, autosomal or pseudoautosomal	Sources Literature Phenotypes ?Thrombocytopenia, anemia, and myelofibrosis 617441
Green MPIG6B in Bleeding and platelet disorders Version 3.10 Latest signed off version: v3.0 (22 Mar 2023)	review	BIALLELIC, autosomal or pseudoautosomal	Sources North West GLH Yorkshire and North East GLH London South GLH NHS GMS Expert Review Green Wessex and West Midlands GLH Phenotypes 617441 ?Thrombocytopenia, anemia, and myelofibrosis
Red MPIG6B in Cytopenia - NOT Fanconi anaemia Version 3.33 Latest signed off version: v3.0 (22 Mar 2023)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Expert review Red Yorkshire and North East GLH North West GLH London South GLH NHS GMS Wessex and West Midlands GLH Phenotypes 617441 Thrombocytopenia, anemia, and myelofibrosis ?Thrombocytopenia, anemia, and myelofibrosis1, 617441 ?Thrombocytopenia, anemia, and myelofibrosis, 617441
Green MPIG6B in Severe Paediatric Disorders Version 1.184	review	BIALLELIC, autosomal or pseudoautosomal	Sources Next Generation Children Project Expert Review Green Expert list Phenotypes Thrombocytopenia, anemia, and myelofibrosis, 617441