Gene: ZNF711 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711 		0.300 Biomarker disease CLINGEN A maternally inherited 8.05 Mb Xq21 deletion associated with Choroideremia, deafness, and mental retardation syndrome in a male patient. 28630650 2017
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711 		0.300 Biomarker disease CLINGEN Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability. 27993705 2017
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711 		0.300 Biomarker disease CLINGEN Fine mapping of Xq11.1-q21.33 and mutation screening of RPS6KA6, ZNF711, ACSL4, DLG3, and IL1RAPL2 for autism spectrum disorders (ASD). 21384559 2011
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711 		0.300 Biomarker disease CLINGEN A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. 19377476 2009