Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6662
Gene Symbol: SOX9
SOX9
0.690 Biomarker disease BEFREE SOX9 haploinsufficiency resulting from breakpoints in a ∼1-Mb region upstream of SOX9 was reported in acampomelic campomelic dysplasia (ACD) patients, suggesting that essential enhancer regions of SOX9 for cartilage development are located in this long non-coding sequence. 30146478 2018
Entrez Id: 6662
Gene Symbol: SOX9
SOX9
0.690 Biomarker disease BEFREE Balanced and unbalanced structural genomic variants with breakpoints mapping up to 1.3 Mb up- and downstream to SOX9 have been described in patients with milder phenotypes, including acampomelic campomelic dysplasia, sex reversal, and Pierre Robin sequence. 28085555 2017
Entrez Id: 6662
Gene Symbol: SOX9
SOX9
0.690 Biomarker disease MGD Discovery and characterization of spontaneous mouse models of craniofacial dysmorphology. 26234751 2016
Entrez Id: 6662
Gene Symbol: SOX9
SOX9
0.690 GeneticVariation disease BEFREE Campomelic dysplasia and acampomelic campomelic dysplasia (ACD) are allelic disorders due to heterozygous mutations in or around SOX9. 26663529 2016
Entrez Id: 6662
Gene Symbol: SOX9
SOX9
0.690 GeneticVariation disease BEFREE The clinical impact of chromosomal rearrangements with breakpoints upstream of the SOX9 gene: two novel de novo balanced translocations associated with acampomelic campomelic dysplasia. 23648064 2013
Entrez Id: 6662
Gene Symbol: SOX9
SOX9
0.690 GeneticVariation disease BEFREE Sex-reversed acampomelic campomelic dysplasia with a homozygous deletion mutation in SOX9 gene. 21962881 2012
Entrez Id: 6662
Gene Symbol: SOX9
SOX9
0.690 GeneticVariation disease BEFREE We tested this approach in three patients with complex chromosomal translocations: The first had craniofacial abnormalities and an apparently balanced t(2;3)(p15;q12) translocation; the second has cleidocranial dysplasia (OMIM 119600) associated with a t(2;6)(q22;p12.3) translocation and a breakpoint in RUNX2 on chromosome 6p; and the third has acampomelic campomelic dysplasia (OMIM 114290) associated with a t(5;17)(q23.2;q24) translocation, with a breakpoint upstream of SOX9 on chromosome 17q. 21890680 2011
Entrez Id: 6662
Gene Symbol: SOX9
SOX9
0.690 GeneticVariation disease BEFREE Translocation and deletion around SOX9 in a patient with acampomelic campomelic dysplasia and sex reversal. 20453475 2010
Entrez Id: 6662
Gene Symbol: SOX9
SOX9
0.690 Biomarker disease BEFREE Fine mapping of chromosome 17 translocation breakpoints > or = 900 Kb upstream of SOX9 in acampomelic campomelic dysplasia and a mild, familial skeletal dysplasia. 15717285 2005
Entrez Id: 6662
Gene Symbol: SOX9
SOX9
0.690 Biomarker disease MGD Conditional inactivation of Sox9: a mouse model for campomelic dysplasia. 11857796 2002
Entrez Id: 6662
Gene Symbol: SOX9
SOX9
0.690 Biomarker disease MGD Haploinsufficiency of Sox9 results in defective cartilage primordia and premature skeletal mineralization. 11371614 2001
Entrez Id: 6662
Gene Symbol: SOX9
SOX9
0.690 GeneticVariation disease BEFREE Acampomelic campomelic dysplasia with SOX9 mutation. 10951468 2000
Entrez Id: 6662
Gene Symbol: SOX9
SOX9
0.690 CausalMutation disease CLINVAR
Entrez Id: 6662
Gene Symbol: SOX9
SOX9
0.690 Biomarker disease CTD_human
Entrez Id: 400618
Gene Symbol: SOX9-AS1
SOX9-AS1
0.100 CausalMutation disease CLINVAR
Entrez Id: 860
Gene Symbol: RUNX2
RUNX2
0.010 GeneticVariation disease BEFREE We tested this approach in three patients with complex chromosomal translocations: The first had craniofacial abnormalities and an apparently balanced t(2;3)(p15;q12) translocation; the second has cleidocranial dysplasia (OMIM 119600) associated with a t(2;6)(q22;p12.3) translocation and a breakpoint in RUNX2 on chromosome 6p; and the third has acampomelic campomelic dysplasia (OMIM 114290) associated with a t(5;17)(q23.2;q24) translocation, with a breakpoint upstream of SOX9 on chromosome 17q. 21890680 2011
Entrez Id: 923
Gene Symbol: CD6
CD6
0.010 GeneticVariation disease BEFREE Isolation of a testis-specific cDNA on chromosome 17q from a region adjacent to the breakpoint of t(12;17) observed in a patient with acampomelic campomelic dysplasia and sex reversal. 8789441 1996