ANKS1B

ankyrin repeat and sterile alpha motif domain containing 1B
OMIM: 607815, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber ANKS1B in Intellectual disability


Level 2: Developmental disorders
Version 9.370
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 Amber
    • Literature
    Phenotypes
    • complex neurodevelopmental disorder, MONDO:0100038