1. Genes and Genomic Entities
  2. ADGRL1

ADGRL1

adhesion G protein-coupled receptor L1
OMIM: 616416, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Amber ADGRL1 in Early onset or syndromic epilepsy


Level 2: Neurology
Version 8.170
Latest signed off version: v8.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders
  • Unexplained death in infancy and sudden unexplained death in childhood

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Developmental delay, behavioral abnormalities, and neuropsychiatric disorders, OMIM:620065
    Green ADGRL1 in Intellectual disability


    Level 2: Developmental disorders
    Version 9.355
    Latest signed off version: v9.0 (30 Apr 2025)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • NHS GMS
    • Literature
    Phenotypes
    • Developmental delay, behavioral abnormalities, and neuropsychiatric disorders, OMIM:620065