CXCR2

C-X-C motif chemokine receptor 2
OMIM: 146928, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Amber CXCR2 in Primary immunodeficiency or monogenic inflammatory bowel disease


Version 4.199
Latest signed off version: v4.0 (22 Mar 2023)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • WHIM syndrome 2, OMIM:619407
Tags
  • Q4_23_promote_green
  • Q4_23_NHS_review
Amber CXCR2 in Cytopenia - NOT Fanconi anaemia


Version 3.31
Latest signed off version: v3.0 (22 Mar 2023)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • ?WHIM syndrome 2, OMIM:619407
Tags
  • Q4_23_promote_green
  • Q4_23_NHS_review