ATP2C2

ATPase secretory pathway Ca2+ transporting 2
OMIM: 613082, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red ATP2C2 in Intellectual disability

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 6.13
Latest signed off version: v6.0 (1 May 2024)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Literature
    Phenotypes
    • language impairment, HP:0002463