Gene: SATB2 ×
Source: INFERRED ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23314
Gene Symbol: SATB2
SATB2 		0.100 GeneticVariation phenotype CLINVAR Disorders with similar clinical phenotypes reveal underlying genetic interaction: SATB2 acts as an activator of the UPF3B gene. 23925499 2013
Entrez Id: 23314
Gene Symbol: SATB2
SATB2 		0.100 CausalMutation phenotype CLINVAR 4.5 Mb microdeletion in chromosome band 2q33.1 associated with learning disability and cleft palate. 19576302 2010
Entrez Id: 23314
Gene Symbol: SATB2
SATB2 		0.100 GeneticVariation phenotype CLINVAR 4.5 Mb microdeletion in chromosome band 2q33.1 associated with learning disability and cleft palate. 19576302 2010
Entrez Id: 23314
Gene Symbol: SATB2
SATB2 		0.100 CausalMutation phenotype CLINVAR Small deletions of SATB2 cause some of the clinical features of the 2q33.1 microdeletion syndrome. 19668335 2009
Entrez Id: 23314
Gene Symbol: SATB2
SATB2 		0.100 GeneticVariation phenotype CLINVAR Small deletions of SATB2 cause some of the clinical features of the 2q33.1 microdeletion syndrome. 19668335 2009
Entrez Id: 23314
Gene Symbol: SATB2
SATB2 		0.100 GeneticVariation phenotype CLINVAR Heterozygous nonsense mutation SATB2 associated with cleft palate, osteoporosis, and cognitive defects. 17377962 2007
Entrez Id: 23314
Gene Symbol: SATB2
SATB2 		0.100 CausalMutation phenotype CLINVAR Heterozygous nonsense mutation SATB2 associated with cleft palate, osteoporosis, and cognitive defects. 17377962 2007
Entrez Id: 23314
Gene Symbol: SATB2
SATB2 		0.100 GeneticVariation phenotype CLINVAR Satb2 haploinsufficiency phenocopies 2q32-q33 deletions, whereas loss suggests a fundamental role in the coordination of jaw development. 16960803 2006
Entrez Id: 23314
Gene Symbol: SATB2
SATB2 		0.100 GeneticVariation phenotype CLINVAR SATB2 is a multifunctional determinant of craniofacial patterning and osteoblast differentiation. 16751105 2006
Entrez Id: 23314
Gene Symbol: SATB2
SATB2 		0.100 CausalMutation phenotype CLINVAR SATB2 is a multifunctional determinant of craniofacial patterning and osteoblast differentiation. 16751105 2006
Entrez Id: 23314
Gene Symbol: SATB2
SATB2 		0.100 CausalMutation phenotype CLINVAR Satb2 haploinsufficiency phenocopies 2q32-q33 deletions, whereas loss suggests a fundamental role in the coordination of jaw development. 16960803 2006
Entrez Id: 23314
Gene Symbol: SATB2
SATB2 		0.100 CausalMutation phenotype CLINVAR Identification of SATB2 as the cleft palate gene on 2q32-q33. 12915443 2003
Entrez Id: 23314
Gene Symbol: SATB2
SATB2 		0.100 GeneticVariation phenotype CLINVAR Identification of SATB2 as the cleft palate gene on 2q32-q33. 12915443 2003
Entrez Id: 23314
Gene Symbol: SATB2
SATB2 		0.100 CausalMutation phenotype CLINVAR A locus for isolated cleft palate, located on human chromosome 2q32. 10417281 1999
Entrez Id: 23314
Gene Symbol: SATB2
SATB2 		0.100 GeneticVariation phenotype CLINVAR A locus for isolated cleft palate, located on human chromosome 2q32. 10417281 1999
Entrez Id: 23314
Gene Symbol: SATB2
SATB2 		0.100 CausalMutation phenotype CLINVAR Interstitial deletion of the long arm of chromosome 2 with normal levels of isocitrate dehydrogenase. 2918541 1989
Entrez Id: 23314
Gene Symbol: SATB2
SATB2 		0.100 GeneticVariation phenotype CLINVAR Interstitial deletion of the long arm of chromosome 2 with normal levels of isocitrate dehydrogenase. 2918541 1989
Entrez Id: 23314
Gene Symbol: SATB2
SATB2 		0.100 Biomarker phenotype HPO