ADAMTS9

ADAM metallopeptidase with thrombospondin type 1 motif 9
OMIM: 605421, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels
Amber ADAMTS9 in Tubulointerstitial kidney disease


Level 2: Renal
Version 3.35
Latest signed off version: v3.34 (12 Aug 2026)

Component of the following Super Panels:

  • Unexplained young onset end-stage renal disease
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • NHS GMS
    • Expert Review Amber
    Phenotypes
    • Nephronophthisis-Related Ciliopathy (no OMIM number yet)
    Amber ADAMTS9 in Fetal anomalies


    Level 2: Fetal (including NIPD)
    Version 8.5
    Latest signed off version: v8.0 (12 Aug 2026)

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    Phenotypes
    • ciliopathy
    Green ADAMTS9 in DDG2P


    Version 8.1
    Latest signed off version: v8.0 (12 Aug 2026)

    Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • DD-Gene2Phenotype
    Phenotypes
    • Nephronophthisis Related Ciliopathy
    Tags
    • gene-checked
    Amber ADAMTS9 in Renal ciliopathies


    Level 2: Renal
    Version 5.2
    Latest signed off version: v5.1 (12 Aug 2026)

    Component of the following Super Panels:

  • Cystic renal disease
  • Paediatric disorders
  • Rare multisystem ciliopathy Super panel
  • Unexplained young onset end-stage renal disease
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Expert list
    Phenotypes
    • Nephronophthisis-Related Ciliopathy