SOX9

SRY-box 9
OMIM: 608160, Gene2Phenotype

10 panels

Panel Reviews Mode of inheritance Details
10 panels

Green SOX9 in Skeletal Dysplasia_Fetal


Level 2: Skeletal disorders
Version 0.223

review Unknown
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green
  • Melbourne Genomics Health Alliance Perinatal Autopsy Flagship

Green SOX9 in Differences of Sex Development


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.293

review Unknown
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green

Green SOX9 in Mendeliome


Version 1.1891

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Campomelic dysplasia, MIM# 114290
  • Campomelic dysplasia, MONDO:0007251

Green SOX9 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review Unknown
Sources
  • Genetic Health Queensland
  • Expert Review Green

Green SOX9 in Skeletal dysplasia

Level 3: Skeletal dysplasias
Level 2: Skeletal disorders
Version 0.285

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert Review Green
  • NHS GMS
  • Victorian Clinical Genetics Services
Phenotypes
  • Campomelic dysplasia with autosomal sex reversal 114290
  • Campomelic dysplasia 114290
  • Acampomelic campomelic dysplasia 114290

Green SOX9 in Additional findings_Paediatric


Level 2: Screening
Version 0.278

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • BabySeq Category A gene
  • Expert Review Green
Phenotypes
  • Campomelic dysplasia

Green SOX9 in Clefting disorders

Level 3: Dysmorphic disorders
Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.252

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
  • Radboud University Medical Center, Nijmegen
  • UKGTN
  • Emory Genetics Laboratory
  • Illumina TruGenome Clinical Sequencing Services
Phenotypes
  • CAMPOMELIC DYSPLASIA,114290
  • Campomelic dysplasia with autosomal sex reversal, 114290
  • CAMPOMELIC DYSPLASIA
  • Cleft palate
  • Cleft palate with skeletal abnormalities
  • Orofacial Clefting with Skeletal Features
  • Acampomelic campomelic dysplasia, 114290

Green SOX9 in Hand and foot malformations


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.74

Component of the following Super Panels:

  • Limb and Digital Malformations SuperPanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert list
    • Expert Review Green
    Phenotypes
    • Campomelic dysplasia with autosomal sex reversal 114290

    Green SOX9 in Fetal anomalies


    Version 1.255

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    Phenotypes
    • Campomelic dysplasia with autosomal sex reversal (MIM#114290)
    • Campomelic dysplasia (MIM#114290)
    • Acampomelic campomelic dysplasia (MIM#114290)

    Red SOX9 in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.113

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • BabySeq Category A gene
    Phenotypes
    • Campomelic dysplasia, MIM# 114290