SOX9 Chromosome 17

SRY-box transcription factor 9
125 variants 125 Health Risk

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What This Gene Does
The protein encoded by this gene recognizes the sequence CCTTGAG along with other members of the HMG-box class DNA-binding proteins. It acts during chondrocyte differentiation and, with steroidogenic factor 1, regulates transcription of the anti-Muellerian hormone (AMH) gene. Deficiencies lead to the skeletal malformation syndrome campomelic dysplasia, frequently with sex reversal. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
SRY-box transcription factors
Locus Type
gene with protein product
Location
17q24.3
Ensembl
ENSG00000125398
Associated Conditions (10)
Inborn genetic diseases
Camptomelic dysplasia
SOX9-related disorder
Connective tissue disorder
Neoplasm
Bent bone dysplasia
ACAMPOMELIC CAMPOMELIC DYSPLASIA
CAMPOMELIC DYSPLASIA WITH AUTOSOMAL SEX REVERSAL
Colorectal cancer
See cases
Key Variants
All Variants (125)
RSID Category Clinical Significance Conditions
RS1255573826 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Camptomelic dysplasia, Inborn genetic diseases
RS143697828 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Camptomelic dysplasia, Inborn genetic diseases
RS144824678 Health Risk Conflicting classifications of pathogenicity Camptomelic dysplasia, Camptomelic dysplasia
RS202028563 Health Risk Conflicting classifications of pathogenicity Camptomelic dysplasia, Camptomelic dysplasia
RS202115157 Health Risk Conflicting classifications of pathogenicity Camptomelic dysplasia, Camptomelic dysplasia
RS2143240394 Health Risk Conflicting classifications of pathogenicity Camptomelic dysplasia, Camptomelic dysplasia
RS2229989 Health Risk Conflicting classifications of pathogenicity Camptomelic dysplasia, Inborn genetic diseases, Camptomelic dysplasia
RS367966473 Health Risk Conflicting classifications of pathogenicity Camptomelic dysplasia, SOX9-related disorder, Camptomelic dysplasia
RS370951695 Health Risk Conflicting classifications of pathogenicity
RS542727010 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Camptomelic dysplasia, Inborn genetic diseases
RS564339518 Health Risk Conflicting classifications of pathogenicity Camptomelic dysplasia, Camptomelic dysplasia
RS566929141 Health Risk Conflicting classifications of pathogenicity Camptomelic dysplasia, Camptomelic dysplasia
RS747054712 Health Risk Conflicting classifications of pathogenicity Camptomelic dysplasia, Camptomelic dysplasia
RS749575769 Health Risk Conflicting classifications of pathogenicity Camptomelic dysplasia, Camptomelic dysplasia
RS751690259 Health Risk Conflicting classifications of pathogenicity Camptomelic dysplasia, Inborn genetic diseases, Camptomelic dysplasia
RS754417848 Health Risk Conflicting classifications of pathogenicity Connective tissue disorder, Camptomelic dysplasia, Connective tissue disorder
RS762041707 Health Risk Conflicting classifications of pathogenicity Camptomelic dysplasia, Inborn genetic diseases, Camptomelic dysplasia
RS768210143 Health Risk Conflicting classifications of pathogenicity Camptomelic dysplasia, Camptomelic dysplasia
RS772713612 Health Risk Conflicting classifications of pathogenicity Camptomelic dysplasia, Inborn genetic diseases, Camptomelic dysplasia
RS779386878 Health Risk Conflicting classifications of pathogenicity Connective tissue disorder, Camptomelic dysplasia, Connective tissue disorder
RS866679165 Health Risk Conflicting classifications of pathogenicity Camptomelic dysplasia, Inborn genetic diseases, Camptomelic dysplasia
RS886041242 Health Risk Conflicting classifications of pathogenicity Camptomelic dysplasia, Camptomelic dysplasia, Camptomelic dysplasia
RS1057518419 Health Risk Likely pathogenic
RS1057518669 Health Risk Likely pathogenic Camptomelic dysplasia, Camptomelic dysplasia
RS1064796718 Health Risk Likely pathogenic
RS1555629028 Health Risk Likely pathogenic
RS1555629043 Health Risk Likely pathogenic
RS1555629169 Health Risk Likely pathogenic Neoplasm, Neoplasm
RS1555629370 Health Risk Likely pathogenic
RS1567910317 Health Risk Likely pathogenic
RS1598176416 Health Risk Likely pathogenic
RS1598176495 Health Risk Likely pathogenic
RS1598176531 Health Risk Likely pathogenic
RS1908097162 Health Risk Likely pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1908098789 Health Risk Likely pathogenic Camptomelic dysplasia, Camptomelic dysplasia
RS1908142392 Health Risk Likely pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1908142618 Health Risk Likely pathogenic Camptomelic dysplasia, Camptomelic dysplasia
RS2143236734 Health Risk Likely pathogenic Connective tissue disorder, Connective tissue disorder
RS2143239847 Health Risk Likely pathogenic SOX9-related disorder, SOX9-related disorder
RS2143239984 Health Risk Likely pathogenic
RS2143240089 Health Risk Likely pathogenic Camptomelic dysplasia, Camptomelic dysplasia, Camptomelic dysplasia
RS2143240113 Health Risk Likely pathogenic Camptomelic dysplasia, Camptomelic dysplasia
RS2143240178 Health Risk Likely pathogenic
RS2143240377 Health Risk Likely pathogenic Bent bone dysplasia, Bent bone dysplasia
RS2143240579 Health Risk Likely pathogenic Camptomelic dysplasia, Camptomelic dysplasia
RS2143241065 Health Risk Likely pathogenic Camptomelic dysplasia, Camptomelic dysplasia
RS2143246033 Health Risk Likely pathogenic Camptomelic dysplasia, Camptomelic dysplasia
RS2143247260 Health Risk Likely pathogenic
RS2143251066 Health Risk Likely pathogenic SOX9-related disorder, SOX9-related disorder
RS2143251369 Health Risk Likely pathogenic Camptomelic dysplasia, Camptomelic dysplasia
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