Gene: HTC2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3342
Gene Symbol: HTC2
HTC2 		0.040 Biomarker group BEFREE The results also demonstrate the power of array CGH to further scrutinize the critical gene(s) of del22q11.2 syndrome responsible for heart defects. 23828768 2014
Entrez Id: 3342
Gene Symbol: HTC2
HTC2 		0.040 GeneticVariation group BEFREE Here, we reported a patient with congenital heart defects and a 5.78 Mb terminal deletion of chromosome 15q detected by array-CGH. 21172461 2011
Entrez Id: 3342
Gene Symbol: HTC2
HTC2 		0.040 Biomarker group BEFREE In contrast to GTG banding, array CGH determined the exact number of deleted genes and thus allowed the identification of candidate genes for cleft palate (GREM1, CX36, MEIS2), congenital heart defect (ACTC, GREM1, CX36, MEIS2), and mental retardation (ARHGAP11A, CHRNA7, CHRM5). 17163532 2007
Entrez Id: 3342
Gene Symbol: HTC2
HTC2 		0.040 GeneticVariation group BEFREE Submicroscopic chromosomal imbalances detected by array-CGH are a frequent cause of congenital heart defects in selected patients. 17384091 2007