Gene: MRX49 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4412
Gene Symbol: MRX49
MRX49 		0.030 GeneticVariation disease BEFREE Xp22.3 deletion in males can be associated with short stature (SHOX), chondrodysplasia punctata (ARSE), mental retardation (MRX49 locus), ichthyosis (STS), Kallmann syndrome (KAL1) and ocular albinism (OA1), according to the size of the deletion. 18194880 2008
Entrez Id: 4412
Gene Symbol: MRX49
MRX49 		0.030 Biomarker disease BEFREE In particular, molecular analysis showed that the putative MRX 49 gene for mental retardation is unlikely to be deleted in this case. 11186896 2000
Entrez Id: 4412
Gene Symbol: MRX49
MRX49 		0.030 GeneticVariation disease BEFREE The boy manifested, due to nullisomy of this region, short stature (SHOX), chondrodysplasia punctata (ARSE), and mental retardation (putative mental retardation gene MRX 49). 10232745 1999