NARS

asparaginyl-tRNA synthetase
OMIM: 108410, Gene2Phenotype

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Green NARS in Mendeliome


Version 1.1891

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities (NEDMILG), MIM#619091
  • Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities (NEDMILEG), MIM#619092
  • Abnormal muscle tone
  • Microcephaly
  • Global developmental delay
  • Intellectual disability
  • Seizures
  • Ataxia
  • Abnormality of the face
  • Demyelinating peripheral neuropathy
Tags
  • new gene name

Green NARS in Microcephaly


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.269

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive - MIM#619091
  • Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant - MIM#619092
Tags
  • new gene name

Green NARS in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.33

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities (NEDMILG), MIM#619091
    • Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities (NEDMILEG), MIM#619092
    • Abnormal muscle tone
    • Microcephaly
    • Global developmental delay
    • Intellectual disability
    • Seizures
    • Ataxia
    • Abnormality of the face
    • Demyelinating peripheral neuropathy
    Tags
    • new gene name

    Green NARS in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.6063

    review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities (NEDMILG), MIM#619091
    • Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities (NEDMILEG), MIM#619092
    • Abnormal muscle tone
    • Microcephaly
    • Global developmental delay
    • Intellectual disability
    • Seizures
    • Ataxia
    • Abnormality of the face
    • Demyelinating peripheral neuropathy
    Tags
    • new gene name

    Green NARS in Hereditary Neuropathy - complex


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.14

    Component of the following Super Panels:

  • Hereditary Neuropathy_CMT_IsolatedAndComplex
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions
  • review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities (NEDMILG), MIM#619091
    • Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities (NEDMILEG), MIM#619092
    • Abnormal muscle tone
    • Microcephaly
    • Global developmental delay
    • Intellectual disability
    • Seizures
    • Ataxia
    • Abnormality of the face
    • Demyelinating peripheral neuropathy
    Tags
    • new gene name

    Green NARS in Fetal anomalies


    Version 1.255

    review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive - MIM#619091
    • Neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant - MIM#619092