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 - narrow panel


Version 4.56
Latest signed off version: v4.0 (22 Mar 2023)

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 3: Non-syndromic hearing loss
    Level 2: Hearing and ear disorders
    Version 4.25
    Latest signed off version: v4.0 (22 Mar 2023)

    Component of the following Super Panels:

  • Paediatric disorders
  • review Not set
    Sources
    • Expert
    Amber SLC9A1 in Hereditary ataxia with onset in adulthood


    Version 4.30
    Latest signed off version: v4.0 (22 Mar 2023)

    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