Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57822
Gene Symbol: GRHL3
GRHL3
0.300 SusceptibilityMutation disease ORPHANET Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate. 27018475 2016
Entrez Id: 57822
Gene Symbol: GRHL3
GRHL3
0.300 SusceptibilityMutation disease ORPHANET A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3. 27018472 2016
Entrez Id: 7314
Gene Symbol: UBB
UBB
0.300 GeneticVariation disease ORPHANET Genotype phenotype correlation of 30 patients with Smith-Magenis syndrome (SMS) using comparative genome hybridisation array: cleft palate in SMS is associated with larger deletions. 17468296 2007
Entrez Id: 9968
Gene Symbol: MED12
MED12
0.300 Biomarker disease GENOMICS_ENGLAND Terminal deletion of chromosome 5p in a patient with phenotypical features of Lujan-Fryns syndrome. 12784307 2003
Entrez Id: 22827
Gene Symbol: PUF60
PUF60
0.100 GeneticVariation disease CLINVAR
Entrez Id: 4184
Gene Symbol: SMCP
SMCP
0.020 Biomarker disease BEFREE Each type of cleft (cleft lip [CL], cleft lip and palate [CLP], cleft palate only [CP], and submucous cleft palate only [SMCP]) was associated with different genes. 24437586 2015
Entrez Id: 50945
Gene Symbol: TBX22
TBX22
0.020 GeneticVariation disease BEFREE X-linked cleft palate (CPX) is caused by mutations in the gene encoding the TBX22 transcription factor and is known to exhibit phenotypic variability, usually involving either a complete, partial or submucous cleft palate, with or without ankyloglossia. 22784330 2013
Entrez Id: 50945
Gene Symbol: TBX22
TBX22
0.020 Biomarker disease BEFREE Here, we report a Tbx22(null) mouse, which has a submucous cleft palate (SMCP) and ankyloglossia, similar to the human phenotype, with a small minority showing overt clefts. 19648291 2009
Entrez Id: 4184
Gene Symbol: SMCP
SMCP
0.020 GeneticVariation disease BEFREE Based on these findings, either a radical dissection and retropositioning of the velar muscles (submucous cleft palate [SMCP repair]) or a Hynes pharyngoplasty (posterior pharyngeal wall augmentation pharyngoplasty) was performed. 14989693 2004
Entrez Id: 3664
Gene Symbol: IRF6
IRF6
0.010 Biomarker disease BEFREE Collectively, our data illustrate that persistent Hh signaling in the palatal epithelium contributes to the etiology and pathogenesis of submucous cleft palate through its interaction with a p63/Irf6-dependent biological regulatory loop and through a p63-induced cell adhesion network. 29981310 2018
Entrez Id: 11202
Gene Symbol: KLK8
KLK8
0.010 Biomarker disease BEFREE The distance between the medial pterygoid plates, the HNP, and the WNP were larger in SMCP patients preoperatively (p < 0.05), but these differences disappeared after surgery (p > 0.05). 29709332 2018
Entrez Id: 8692
Gene Symbol: HYAL2
HYAL2
0.010 Biomarker disease BEFREE Consistent with the clinical presentation in affected individuals, investigations of Hyal2-/- mice revealed craniofacial abnormalities, including submucosal cleft palate. 28081210 2017
Entrez Id: 23406
Gene Symbol: COTL1
COTL1
0.010 Biomarker disease BEFREE Each type of cleft (cleft lip [CL], cleft lip and palate [CLP], cleft palate only [CP], and submucous cleft palate only [SMCP]) was associated with different genes. 24437586 2015
Entrez Id: 810
Gene Symbol: CALML3
CALML3
0.010 Biomarker disease BEFREE Each type of cleft (cleft lip [CL], cleft lip and palate [CLP], cleft palate only [CP], and submucous cleft palate only [SMCP]) was associated with different genes. 24437586 2015
Entrez Id: 8048
Gene Symbol: CSRP3
CSRP3
0.010 Biomarker disease BEFREE Each type of cleft (cleft lip [CL], cleft lip and palate [CLP], cleft palate only [CP], and submucous cleft palate only [SMCP]) was associated with different genes. 24437586 2015
Entrez Id: 7043
Gene Symbol: TGFB3
TGFB3
0.010 Biomarker disease BEFREE The analysis of genetic variants hints at the contribution of TGFB3 and MN1 in the aetiology of SMCPs. 22409215 2012