Source: CLINGEN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711
CUI: C3501611
Disease: Mental Retardation, X-Linked Nonsyndromic
Mental Retardation, X-Linked Nonsyndromic 		0.300 Biomarker 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
CUI: C3501611
Disease: Mental Retardation, X-Linked Nonsyndromic
Mental Retardation, X-Linked Nonsyndromic 		0.300 Biomarker 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
CUI: C3501611
Disease: Mental Retardation, X-Linked Nonsyndromic
Mental Retardation, X-Linked Nonsyndromic 		0.300 Biomarker 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
CUI: C3501611
Disease: Mental Retardation, X-Linked Nonsyndromic
Mental Retardation, X-Linked Nonsyndromic 		0.300 Biomarker CLINGEN A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. 19377476

2009