Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.400 GeneticVariation phenotype CLINVAR MECP2 mutations in males. 17351020 2007
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.400 GeneticVariation phenotype CLINVAR Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2. 17267601 2007
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.400 GeneticVariation phenotype CLINVAR Chromosomal copy number changes in patients with non-syndromic X linked mental retardation detected by array CGH. 16169931 2006
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.400 CausalMutation phenotype CLINVAR Chromosomal copy number changes in patients with non-syndromic X linked mental retardation detected by array CGH. 16169931 2006
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.400 CausalMutation phenotype CLINVAR Male Rett phenotypes in T158M and R294X MeCP2-mutations. 17236109 2006
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.400 GeneticVariation phenotype CLINVAR Male Rett phenotypes in T158M and R294X MeCP2-mutations. 17236109 2006
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.400 GeneticVariation phenotype CLINVAR Early progressive encephalopathy in boys and MECP2 mutations. 16832102 2006
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.400 CausalMutation phenotype CLINVAR Early progressive encephalopathy in boys and MECP2 mutations. 16832102 2006
Entrez Id: 10943
Gene Symbol: MSL3
MSL3 		0.400 GeneticVariation phenotype CLINVAR The MRG domain mediates the functional integration of MSL3 into the dosage compensation complex. 15988010 2005
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.400 GeneticVariation phenotype CLINVAR Macrocephalic mental retardation associated with a novel C-terminal MECP2 frameshift deletion. 15558314 2005
Entrez Id: 10943
Gene Symbol: MSL3
MSL3 		0.400 GeneticVariation phenotype CLINVAR A human protein complex homologous to the Drosophila MSL complex is responsible for the majority of histone H4 acetylation at lysine 16. 16227571 2005
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.400 CausalMutation phenotype CLINVAR Macrocephalic mental retardation associated with a novel C-terminal MECP2 frameshift deletion. 15558314 2005
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.400 GeneticVariation phenotype CLINVAR Phenotypic manifestations of MECP2 mutations in classical and atypical Rett syndrome. 15057977 2004
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.400 CausalMutation phenotype CLINVAR Phenotypic manifestations of MECP2 mutations in classical and atypical Rett syndrome. 15057977 2004
Entrez Id: 3954
Gene Symbol: LETM1
LETM1 		0.400 Biomarker phenotype CTD_human The leucine zipper-, EF-hand-containing transmembrane protein 1 (LETM1) has recently been cloned in an attempt to identify genes deleted in Wolf-Hirschhorn syndrome (WHS), a microdeletion syndrome characterized by severe growth and mental retardation, hypotonia, seizures, and typical facial dysmorphic features. 14706454 2004
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.400 GeneticVariation phenotype CLINVAR Neurodevelopmental disorders in males related to the gene causing Rett syndrome in females (MECP2). 12615169 2003
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.400 CausalMutation phenotype CLINVAR Neurodevelopmental disorders in males related to the gene causing Rett syndrome in females (MECP2). 12615169 2003
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.400 CausalMutation phenotype CLINVAR DNA recognition by the methyl-CpG binding domain of MeCP2. 11035019 2001
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.400 GeneticVariation phenotype CLINVAR Epilepsy in a representative series of Rett syndrome. 11227330 2001
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.400 CausalMutation phenotype CLINVAR Epilepsy in a representative series of Rett syndrome. 11227330 2001
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.400 GeneticVariation phenotype CLINVAR DNA recognition by the methyl-CpG binding domain of MeCP2. 11035019 2001
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.400 GeneticVariation phenotype CLINVAR Functional consequences of Rett syndrome mutations on human MeCP2. 11058114 2000
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.400 CausalMutation phenotype CLINVAR Functional consequences of Rett syndrome mutations on human MeCP2. 11058114 2000
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.400 GeneticVariation phenotype CLINVAR Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. 10508514 1999
Entrez Id: 4204
Gene Symbol: MECP2
MECP2 		0.400 CausalMutation phenotype CLINVAR Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. 10508514 1999