Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9275
Gene Symbol: BCL7B
BCL7B
CUI: C0175702
Disease: Williams Syndrome
Williams Syndrome 		0.030 Biomarker BEFREE Further, we have assessed transcriptome sequence data and found evidence that MEIs impact the expression levels of six genes (WBSCR17, LIMK1, GTF2I, WBSCR27, BAZ1B, and BCL7B), all of which have known roles in human Williams-Beuren syndrome due to changes in copy number, typically hemizygosity. 29860323

2018
Entrez Id: 9275
Gene Symbol: BCL7B
BCL7B
CUI: C0175702
Disease: Williams Syndrome
Williams Syndrome 		0.030 Biomarker BEFREE Although several studies have suggested that malignant diseases occurring in patients with Williams-Beuren syndrome are associated with aberrations in BCL7B, little is known regarding the function of this gene at the cellular level. 25569233

2015
Entrez Id: 9275
Gene Symbol: BCL7B
BCL7B
CUI: C0175702
Disease: Williams Syndrome
Williams Syndrome 		0.030 GeneticVariation BEFREE The BCL7 gene family: deletion of BCL7B in Williams syndrome. 9931421

1998