TLR7

toll like receptor 7
OMIM: 300365, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Red TLR7 in Familial Meniere Disease

Level 3: Other hearing and ear disorders
Level 2: Hearing and ear disorders
Version 1.4

review Not set
Sources
  • Literature
Green TLR7 in COVID-19 research


Level 2: Viral research
Version 1.146

review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • OMIM
  • Expert list
Green TLR7 in Primary immunodeficiency or monogenic inflammatory bowel disease


Level 2: Immunology
Version 8.78
Latest signed off version: v8.0 (30 Apr 2025)

review X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Sources
  • NHS GMS
  • Expert Review Green
  • Literature
Phenotypes
  • Systemic lupus erythematosus 17, OMIM:301080
  • Immunodeficiency 74, COVID19-related, X-linked, OMIM:301051