ATP9A

ATPase phospholipid transporting 9A (putative)
OMIM: 609126, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green ATP9A in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Neurodevelopmental disorder with poor growth and behavioural abnormalities, MIM# 620242

Green ATP9A in Microcephaly


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.269

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Neurodevelopmental disorder with poor growth and behavioural abnormalities, MIM# 620242

Green ATP9A in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Neurodevelopmental disorder with poor growth and behavioural abnormalities, MIM# 620242

Amber ATP9A in Fetal anomalies


Version 1.255

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Neurodevelopmental disorder with poor growth and behavioural abnormalities, MIM# 620242