1. Genes and Genomic Entities
  2. NAA60

NAA60

N(alpha)-acetyltransferase 60, NatF catalytic subunit
OMIM: 614246, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels
Green NAA60 in White matter disorders and cerebral calcification - narrow panel


Level 2: Neurology
Version 7.13
Latest signed off version: v7.0 (30 Apr 2025)

Component of the following Super Panels:

  • Childhood onset leukodystrophy

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • NHS GMS
    • Literature
    Phenotypes
    • Basal ganglia calcification, idiopathic, 9, autosomal recessive, OMIM:620786
    • basal ganglia calcification, idiopathic, 9, autosomal recessive, MONDO:0968977
    Green NAA60 in Adult onset neurodegenerative disorder


    Level 2: Neurology
    Version 8.11
    Latest signed off version: v8.0 (30 Apr 2025)

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • NHS GMS
    • Literature
    Phenotypes
    • Basal ganglia calcification, idiopathic, 9, autosomal recessive, OMIM:620786
    • basal ganglia calcification, idiopathic, 9, autosomal recessive, MONDO:0968977
    Red NAA60 in Intellectual disability


    Level 2: Developmental disorders
    Version 9.285
    Latest signed off version: v9.0 (30 Apr 2025)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Basal ganglia calcification, idiopathic, 9, autosomal recessive, OMIM:620786
    • basal ganglia calcification, idiopathic, 9, autosomal recessive, MONDO:0968977
    Green NAA60 in Hereditary ataxia with onset in adulthood


    Level 2: Neurology
    Version 8.23
    Latest signed off version: v8.0 (30 Apr 2025)

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • NHS GMS
    • Literature
    Phenotypes
    • Basal ganglia calcification, idiopathic, 9, autosomal recessive, OMIM:620786
    • basal ganglia calcification, idiopathic, 9, autosomal recessive, MONDO:0968977