Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 11141
Gene Symbol: IL1RAPL1
IL1RAPL1 		0.580 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 65109
Gene Symbol: UPF3B
UPF3B 		0.520 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711 		0.520 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 116442
Gene Symbol: RAB39B
RAB39B 		0.510 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 6855
Gene Symbol: SYP
SYP 		0.500 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 5063
Gene Symbol: PAK3
PAK3 		0.340 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 254065
Gene Symbol: BRWD3
BRWD3 		0.310 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 347344
Gene Symbol: ZNF81
ZNF81 		0.310 Biomarker disease GENOMICS_ENGLAND
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: 6535
Gene Symbol: SLC6A8
SLC6A8 		0.370 GeneticVariation disease BEFREE X-linked mental retardation with seizures and carrier manifestations is caused by a mutation in the creatine-transporter gene (SLC6A8) located in Xq28. 11898126 2002
Entrez Id: 6535
Gene Symbol: SLC6A8
SLC6A8 		0.370 GeneticVariation disease LHGDN X-linked mental retardation with seizures and carrier manifestations is caused by a mutation in the creatine-transporter gene (SLC6A8) located in Xq28. 11898126 2002
Entrez Id: 57502
Gene Symbol: NLGN4X
NLGN4X 		0.010 GeneticVariation disease BEFREE X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family. 14963808 2004
Entrez Id: 10084
Gene Symbol: PQBP1
PQBP1 		0.400 GeneticVariation disease BEFREE X-linked mental retardation has been traditionally divided into syndromic (S-XLMR) and non-syndromic forms (NS-XLMR), although the borderlines between these phenotypes begin to vanish and mutations in a single gene, for example PQBP1, can cause S-XLMR as well as NS-XLMR. 17033686 2007
Entrez Id: 1183
Gene Symbol: CLCN4
CLCN4 		0.010 GeneticVariation disease BEFREE X-linked mental retardation with neonatal hypotonia in a French family (MRX15): gene assignment to Xp11.22-Xp21.1. 8826458 1996
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: 2182
Gene Symbol: ACSL4
ACSL4 		0.040 GeneticVariation disease BEFREE FACL4, encoding fatty acid-CoA ligase 4, is mutated in nonspecific X-linked mental retardation. 11889465 2002
Entrez Id: 2182
Gene Symbol: ACSL4
ACSL4 		0.040 GeneticVariation disease LHGDN FACL4, encoding fatty acid-CoA ligase 4, is mutated in nonspecific X-linked mental retardation. 11889465 2002
Entrez Id: 186
Gene Symbol: AGTR2
AGTR2 		0.320 GeneticVariation disease LHGDN AGTR2 mutations in X-linked mental retardation. 12089445 2002
Entrez Id: 186
Gene Symbol: AGTR2
AGTR2 		0.320 Biomarker disease CTD_human AGTR2 mutations in X-linked mental retardation. 12089445 2002
Entrez Id: 186
Gene Symbol: AGTR2
AGTR2 		0.320 GeneticVariation disease BEFREE AGTR2 mutations in X-linked mental retardation. 12089445 2002
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.100 GeneticVariation disease BEFREE MECP2 gene mutations in non-syndromic X-linked mental retardation: phenotype-genotype correlation. 14598336 2003
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.100 GeneticVariation disease LHGDN MECP2 gene mutations in non-syndromic X-linked mental retardation: phenotype-genotype correlation. 14598336 2003
Entrez Id: 65267
Gene Symbol: WNK3
WNK3 		0.010 GeneticVariation disease LHGDN WNK3 lies within the critical linkage interval for several human monogenic disorders, including X-linked mental retardation. 15194194 2004
Entrez Id: 11141
Gene Symbol: IL1RAPL1
IL1RAPL1 		0.580 GeneticVariation disease BEFREE IL1RAPL1 (interleukin-1 receptor accessory protein-like, gene 1) has recently been shown to be mutated in patients with X-linked mental retardation. 15300857 2004
Entrez Id: 4983
Gene Symbol: OPHN1
OPHN1 		0.400 GeneticVariation disease LHGDN Oligophrenin 1 mutations were found in 12% (2/17) of individuals with mental retardatin and known cerebellar anomalies and in 1% (2/196) of the X-linked mental retardation group. 16221952 2005