Gene: FTSJ1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 24140
Gene Symbol: FTSJ1
FTSJ1 		0.300 Biomarker disease CLINGEN Defects in tRNA Anticodon Loop 2'-O-Methylation Are Implicated in Nonsyndromic X-Linked Intellectual Disability due to Mutations in FTSJ1. 26310293 2015
Entrez Id: 24140
Gene Symbol: FTSJ1
FTSJ1 		0.300 Biomarker disease CLINGEN A loss-of-function mutation in the FTSJ1 gene causes nonsyndromic X-linked mental retardation in a Japanese family. 18081026 2008
Entrez Id: 24140
Gene Symbol: FTSJ1
FTSJ1 		0.300 Biomarker disease CLINGEN Mutations in the FTSJ1 gene coding for a novel S-adenosylmethionine-binding protein cause nonsyndromic X-linked mental retardation. 15162322 2004
Entrez Id: 24140
Gene Symbol: FTSJ1
FTSJ1 		0.300 Biomarker disease CLINGEN A splice site mutation in the methyltransferase gene FTSJ1 in Xp11.23 is associated with non-syndromic mental retardation in a large Belgian family (MRX9). 15342698 2004
Entrez Id: 24140
Gene Symbol: FTSJ1
FTSJ1 		0.300 Biomarker disease CLINGEN Family MRX9 revisited: further evidence for locus heterogeneity in MRX. 12239714 2002
Entrez Id: 24140
Gene Symbol: FTSJ1
FTSJ1 		0.300 Biomarker disease CLINGEN Four families (MRX43, MRX44, MRX45, MRX52) with nonspecific X-linked mental retardation: clinical and psychometric data and results of linkage analysis. 10398246 1999
Entrez Id: 24140
Gene Symbol: FTSJ1
FTSJ1 		0.300 Biomarker disease CLINGEN Localization of a gene responsible for nonspecific mental retardation (MRX9) to the pericentromeric region of the X chromosome. 8288232 1993