IL1RAPL2

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

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red IL1RAPL2 in Autism


Version 0.36

review Not set
Sources
  • Expert Review Red
  • SFARI
Amber IL1RAPL2 in Intellectual disability

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 6.13
Latest signed off version: v6.0 (1 May 2024)

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