1. Genes and Genomic Entities
  2. STX1A

STX1A

syntaxin 1A
OMIM: 186590, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Green STX1A in DDG2P


Version 7.1
Latest signed off version: v7.0 (6 May 2026)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • DD-Gene2Phenotype
    • Expert Review Green
    Phenotypes
    • STX1A-associated neurodevelopmental disorder with epilepsy
    • STX1A-associated neurodevelopmental disorder without epilepsy
    Tags
    • gene-checked
    Green STX1A in Intellectual disability


    Level 2: Developmental disorders
    Version 10.16
    Latest signed off version: v10.0 (6 May 2026)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • NHS GMS
    • Literature
    Phenotypes
    • neurodevelopmental disorder, MONDO:0700092
    • intellectual disability, MONDO:0001071
    Tags
    • gene-checked