1. Genes and Genomic Entities
  2. RUNX1T1

RUNX1T1

RUNX1 translocation partner 1
OMIM: 133435, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber RUNX1T1 in Intellectual disability


Level 2: Developmental disorders
Version 9.279
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
    • neurodevelopmental disorder, MONDO:0700092
    • intellectual disability, MONDO:0001071