Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 64221
Gene Symbol: ROBO3
ROBO3
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.190 GeneticVariation LHGDN Neurologic features of horizontal gaze palsy and progressive scoliosis with mutations in ROBO3. 15824346

2005

Entrez Id: 64221
Gene Symbol: ROBO3
ROBO3
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.190 GeneticVariation BEFREE Neurologic features of horizontal gaze palsy and progressive scoliosis with mutations in ROBO3. 15824346

2005

Entrez Id: 64221
Gene Symbol: ROBO3
ROBO3
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.190 GeneticVariation LHGDN Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis. 15105459

2004

Entrez Id: 64221
Gene Symbol: ROBO3
ROBO3
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.190 Biomarker HPO

Entrez Id: 79628
Gene Symbol: SH3TC2
SH3TC2
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.140 GeneticVariation BEFREE Implication of the SH3TC2 gene in Charcot-Marie-Tooth disease associated with deafness and/or scoliosis: Illustration with four new pathogenic variants. 31634715

2019

Entrez Id: 79628
Gene Symbol: SH3TC2
SH3TC2
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.140 GeneticVariation BEFREE Scoliosis and cranial nerve involvement are frequent features of this CMT4 subtype, and their presence should prompt the clinician to look for SH3TC2 gene mutations. 27231023

2016

Entrez Id: 79628
Gene Symbol: SH3TC2
SH3TC2
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.140 Biomarker BEFREE The absence of scoliosis or late-onset symptoms should not exclude SH3TC2 from the list of candidate genes under consideration. 25737037

2015

Entrez Id: 79628
Gene Symbol: SH3TC2
SH3TC2
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.140 GeneticVariation BEFREE Mutations in SH3TC2 (KIAA1985) cause Charcot-Marie-Tooth disease (CMT) type 4C, a demyelinating inherited neuropathy characterized by early-onset and scoliosis. 19744956

2009

Entrez Id: 79628
Gene Symbol: SH3TC2
SH3TC2
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.140 Biomarker HPO

Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.130 GeneticVariation BEFREE Mutations of PIEZO2 gene have been reported to be associated with progressive scoliosis and impaired proprioception. 31513102

2020

Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.130 GeneticVariation BEFREE A novel nonsense PIEZO2 mutation in a family with scoliosis and proprioceptive defect. 30578100

2019

Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.130 GeneticVariation BEFREE Loss-of-function mutations in the human PIEZO2 gene cause an autosomal recessive syndrome of muscular atrophy with perinatal respiratory distress, arthrogryposis, and scoliosis. 28728825

2017

Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.130 GeneticVariation BEFREE Severe MECP2 mutations (R106W, R168X, R255X, R270X, and large deletions) showed a higher proportion of scoliosis. 28347601

2017

Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.130 GeneticVariation BEFREE Two common methyl-CpG-binding protein 2 (MECP2) mutations, R294X and R306C, had reduced risk for scoliosis. 20032810

2010

Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.130 GeneticVariation BEFREE Methyl-CpG-binding 2 (MECP2) mutations, skeletal fractures, and scoliosis were documented. 18535484

2008

Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.130 CausalMutation CLINVAR

Entrez Id: 63895
Gene Symbol: PIEZO2
PIEZO2
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.130 Biomarker HPO

Entrez Id: 4204
Gene Symbol: MECP2
MECP2
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.130 Biomarker HPO

Entrez Id: 6774
Gene Symbol: STAT3
STAT3
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.120 Biomarker BEFREE Signal transducer and activator of transcription 3 (Stat3), a conserved controller of cell proliferation, survival and regeneration, is associated with human scoliosis, cancer and Hyper IgE Syndrome. 28222105

2017

Entrez Id: 1277
Gene Symbol: COL1A1
COL1A1
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.120 GeneticVariation BEFREE Moderate to severe scoliosis (Cobb angle ≥25°) was rare in individuals with COL1A1 haploinsufficiency mutations but was present in about two fifth of patients with triple helical glycine substitutions or C-propeptide mutations. 26927310

2016

Entrez Id: 2395
Gene Symbol: FXN
FXN
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.120 GeneticVariation BEFREE We compared the patient's clinical data to expansion/deletion carriers available in the literature and suggest that, in clinical practice, the FXN deletion test should be taken into account in patients with early-onset, rapid progressive ataxia and severe scoliosis. 26906906

2016

Entrez Id: 1277
Gene Symbol: COL1A1
COL1A1
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.120 GeneticVariation BEFREE Systematic follow-up of growing patients with COL1A1 haploinsufficiency mutations including radiographic screening for vertebral compression fractures and scoliosis is warranted. 23529829

2013

Entrez Id: 7040
Gene Symbol: TGFB1
TGFB1
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.120 GeneticVariation BEFREE Moreover, we found sexual dimorphisms in the relationships of SNP C-509T of the TGFB1 gene with both the age of disease onset and curve severity: the polymorphism was found to determine both an early onset of scoliosis and the severity of curvature in females but not in males (P < 0.05). 23446766

2013

Entrez Id: 6774
Gene Symbol: STAT3
STAT3
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.120 Biomarker BEFREE Further understanding of how STAT3 results in the diverse manifestations of HIES will allow us to develop more specific therapies for HIES as well as for many of the manifestations, such as scoliosis, recurrent staphylococcal infections, and eczema, which are common in the general population. 19190525

2009

Entrez Id: 2395
Gene Symbol: FXN
FXN
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.120 Biomarker BEFREE Frataxin insufficiency leads to mitochrondrial dysfunction and progressive neurodegeneration, along with scoliosis, diabetes and cardiomyopathy. 17826840

2007