FCGR3B

Fc fragment of IgG receptor IIIb
OMIM: 610665, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels
Red FCGR3B in COVID-19 research


Level 2: Viral research
Version 1.142

review Unknown
Sources
  • Expert Review Red
  • Congenital neutropaenia v1.22
  • GRID V2.0
  • ESID Registry 20171117
  • ESID Registry 20171117
  • GRID V2.0
  • Congenital neutropaenia v1.22
Phenotypes
  • Neutropenia,alloimmuneneonatal
  • Neutropenia, autoimmune neonatal
  • Neutropenia, alloimmune neonatal
  • Fc receptor deficiencies
Red FCGR3B in Primary immunodeficiency or monogenic inflammatory bowel disease


Version 5.3
Latest signed off version: v5.0 (1 May 2024)

review Unknown
Sources
  • Expert Review Red
  • ESID Registry 20171117
  • GRID V2.0
  • Congenital neutropaenia v1.22
Phenotypes
  • Neutropenia,alloimmuneneonatal
  • Neutropenia, alloimmune neonatal
  • Fc receptor deficiencies
  • Neutropenia, autoimmune neonatal
  • Neutropenia, autoimmune neonatal
Red FCGR3B in Cytopenias and congenital anaemias

Level 3: Anaemias and red cell disorders
Level 2: Haematological disorders
Version 1.118

review Other - please specify in evaluation comments
Sources
  • Expert Review Red
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • Neutropenia,alloimmuneneonatal
Red FCGR3B in Cytopenia - NOT Fanconi anaemia


Version 3.34
Latest signed off version: v3.0 (22 Mar 2023)

review Other - please specify in evaluation comments
Sources
  • Expert Review Red
  • NHS GMS
  • Wessex and West Midlands GLH
Phenotypes
  • Neutropenia,alloimmuneneonatal
Green FCGR3B 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
  • Neutropenia, alloimmune neonatal