RUNX1T1

RUNX1 translocation partner 1
OMIM: 133435, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green RUNX1T1 in Mendeliome


Version 1.2374

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Neurodevelopmental disorder MONDO:0700092, RUNX1T1-related

Green RUNX1T1 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 1.83

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Neurodevelopmental disorder MONDO:0700092, RUNX1T1-related