IL1RAPL2

interleukin 1 receptor accessory protein like 2
OMIM: 300277, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber IL1RAPL2 in Intellectual disability


Level 2: Developmental disorders
Version 9.285
Latest signed off version: v9.0 (30 Apr 2025)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • X-linked non-syndromic mental retardation loci
    Tags
    • deletions