Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 347344
Gene Symbol: ZNF81
ZNF81 		0.310 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 347344
Gene Symbol: ZNF81
ZNF81 		0.310 Biomarker disease BEFREE ZNF674 belongs to a cluster of seven highly related zinc-finger genes in Xp11, two of which (ZNF41 and ZNF81) were implicated previously in XLMR. 16385466 2006
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711 		0.520 Biomarker disease CTD_human The screen has discovered nine genes implicated in XLMR, including SYP, ZNF711 and CASK reported here, confirming the power of this strategy. 19377476 2009
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711 		0.520 GeneticVariation disease BEFREE X-linked mental retardation: evidence for a recent mutation in a five-generation family (MRX65) linked to the pericentromeric region. 10398247 1999
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711 		0.520 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711 		0.520 AlteredExpression disease BEFREE A functional link between the histone demethylase PHF8 and the transcription factor ZNF711 in X-linked mental retardation. 20346720 2010
Entrez Id: 641339
Gene Symbol: ZNF674
ZNF674 		0.510 GeneticVariation disease BEFREE We characterized the complete ZNF674 gene structure and subsequently tested an additional 306 patients with XLMR for mutations by direct sequencing. 16385466 2006
Entrez Id: 641339
Gene Symbol: ZNF674
ZNF674 		0.510 Biomarker disease CTD_human We characterized the complete ZNF674 gene structure and subsequently tested an additional 306 patients with XLMR for mutations by direct sequencing. 16385466 2006
Entrez Id: 641339
Gene Symbol: ZNF674
ZNF674 		0.510 Biomarker disease GENOMICS_ENGLAND XLID-causing mutations and associated genes challenged in light of data from large-scale human exome sequencing. 23871722 2013
Entrez Id: 641339
Gene Symbol: ZNF674
ZNF674 		0.510 Biomarker disease LHGDN We characterized the complete ZNF674 gene structure and subsequently tested an additional 306 patients with XLMR for mutations by direct sequencing. 16385466 2006
Entrez Id: 7592
Gene Symbol: ZNF41
ZNF41 		0.520 GeneticVariation disease BEFREE Mutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardation. 14628291 2003
Entrez Id: 7592
Gene Symbol: ZNF41
ZNF41 		0.520 Biomarker disease BEFREE ZNF674 belongs to a cluster of seven highly related zinc-finger genes in Xp11, two of which (ZNF41 and ZNF81) were implicated previously in XLMR. 16385466 2006
Entrez Id: 7592
Gene Symbol: ZNF41
ZNF41 		0.520 Biomarker disease GENOMICS_ENGLAND XLID-causing mutations and associated genes challenged in light of data from large-scale human exome sequencing. 23871722 2013
Entrez Id: 7592
Gene Symbol: ZNF41
ZNF41 		0.520 Biomarker disease CTD_human Mutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardation. 14628291 2003
Entrez Id: 9203
Gene Symbol: ZMYM3
ZMYM3 		0.330 GeneticVariation disease BEFREE ZNF261 at Xq13.1 is disrupted by a t(X;13)(q13.1;q32) rearrangement in a mentally retarded patient and is a candidate gene for nonspecific X-linked mental retardation. 10486218 1999
Entrez Id: 9203
Gene Symbol: ZMYM3
ZMYM3 		0.330 Biomarker disease BEFREE Cloning and characterization of DXS6673E, a candidate gene for X-linked mental retardation in Xq13.1. 8817323 1996
Entrez Id: 9203
Gene Symbol: ZMYM3
ZMYM3 		0.330 Biomarker disease BEFREE FIM is related to DXS6673E, a candidate gene for X-linked mental retardation in Xq13.1; this defines a gene family involved in different human pathologies. 9576949 1998
Entrez Id: 9203
Gene Symbol: ZMYM3
ZMYM3 		0.330 Biomarker disease GENOMICS_ENGLAND Cloning and characterization of DXS6673E, a candidate gene for X-linked mental retardation in Xq13.1. 8817323 1996
Entrez Id: 7750
Gene Symbol: ZMYM2
ZMYM2 		0.010 Biomarker disease BEFREE The predicted RAMP protein exhibits strong homology to the product of a recently cloned candidate gene for X-linked mental retardation, DXS6673E . 9499416 1998
Entrez Id: 51114
Gene Symbol: ZDHHC9
ZDHHC9 		0.010 GeneticVariation disease BEFREE Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitus. 17436253 2007
Entrez Id: 158866
Gene Symbol: ZDHHC15
ZDHHC15 		0.010 GeneticVariation disease BEFREE We suggest that the absence of the ZDHHC15 transcripts in this patient contributes to her phenotype, and that the gene is a strong candidate for nonsyndromic XLMR. 15915161 2005
Entrez Id: 170261
Gene Symbol: ZCCHC12
ZCCHC12 		0.030 GeneticVariation disease BEFREE Mutations in Sizn1 (Zcchc12), a novel transcriptional co-activator in the BMP signaling pathway, are associated with X-linked mental retardation. 19416967 2009
Entrez Id: 170261
Gene Symbol: ZCCHC12
ZCCHC12 		0.030 Biomarker disease LHGDN Our data implicate SIZN1 as a candidate gene for XLMR and/or as a neurocognitive functional modifier. 18798319 2008
Entrez Id: 170261
Gene Symbol: ZCCHC12
ZCCHC12 		0.030 GeneticVariation disease BEFREE Furthermore, mutations in SIZN1 have been associated with X-linked mental retardation. 21172456 2011
Entrez Id: 170261
Gene Symbol: ZCCHC12
ZCCHC12 		0.030 Biomarker disease BEFREE Our data implicate SIZN1 as a candidate gene for XLMR and/or as a neurocognitive functional modifier. 18798319 2008