1. Genes and Genomic Entities
  2. CLEC16A

CLEC16A

C-type lectin domain containing 16A
OMIM: 611303, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber CLEC16A in Intellectual disability

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 6.11
Latest signed off version: v6.0 (1 May 2024)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • severe neurodevelopmental disorder including microcephaly, brain atrophy, corpus callosum dysgenesis, and growth retardation
    Tags
    • Q1_24_promote_green