1. Genes and Genomic Entities
  2. SLC9A1

SLC9A1

solute carrier family 9 member A1
OMIM: 107310, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Green SLC9A1 in Ataxia and cerebellar anomalies - childhood onset


Level 2: Neurology
Version 9.32
Latest signed off version: v9.22 (12 Aug 2026)

Component of the following Super Panels:

  • Hereditary ataxia and cerebellar anomalies, childhood onset

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • NHS GMS
    • Expert Review Green
    • Expert list
    Phenotypes
    • Lichtenstein-Knorr syndrome OMIM:616291
    • Lichtenstein-Knorr syndrome MONDO:0014572
    Red SLC9A1 in Monogenic hearing loss


    Level 2: Audiology
    Version 6.42
    Latest signed off version: v6.34 (12 Aug 2026)

    Component of the following Super Panels:

  • Paediatric disorders

    		•  review Not set
    Sources
    • Expert
    Amber SLC9A1 in Hereditary ataxia, adult onset


    Level 2: Neurology
    Version 9.11
    Latest signed off version: v9.4 (12 Aug 2026)

    Component of the following Super Panels:

  • Adult-onset neurological disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • London North GLH
    • NHS GMS
    • Wessex and West Midlands GLH
    Phenotypes
    • Lichtenstein-Knorr syndrome OMIM:616291
    • Lichtenstein-Knorr syndrome MONDO:0014572