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    MRX2 mental retardation, X-linked 2 (non-dysmorphic) [ Homo sapiens (human) ]

    Gene ID: 4367, updated on 26-Feb-2013
    Official Symbol
    MRX2provided by HGNC
    Official Full Name
    mental retardation, X-linked 2 (non-dysmorphic)provided by HGNC
    Primary source
    HGNC:7249
    See related
    MIM:300428
    Gene type
    unknown
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Annotation information
    Annotation category: not annotated on reference assembly
    Location :
    Xp22.3-p22.2
    See MRX2 in MapViewer

    Related articles in PubMed

    1. Linkage analysis suggests at least two loci for X-linked non-specific mental retardation. Arveiler B, et al. Am J Med Genet, 1988 May-Jun. PMID 3177465.
    2. Nomenclature guidelines for X-linked mental retardation. Mulley JC, et al. Am J Med Genet, 1992 Apr 15-May 1. PMID 1605216.

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    Molecular Biology Databases

      Supplemental Content

      Table of contents

      Related information

      • Map Viewer
        These links are maintained by the Map Viewer group and are provided when a GeneID is annotated on a map for the same species.
      • OMIM
        Links between OMIM and Gene are calculated by Gene based on MIM numbers included in the summary and phenotype sections of the Gene record.
      • PubMed
        Links between Gene and PubMed are the result of the following: 1. Manual curation within NCBI. Part of the process of generating a REVIEWED RefSeq is an analysis of the current literature. Papers that are seminal in defining the gene, its sequence, and its function are added to the record at that time. Alert users point out gaps or errors in papers associated with a Gene record. These messages are reviewed and implemented as required. 2. Integration of information from other public databases. Gene integrates gene-citation from resources external to NCBI such as model organism-specific databases, Gene Ontology (GO), groups curating interactions, and sequence databases. The assumption in using these source is that they report citations specific to a gene in a known species. Gene does not process citations from OMIM automatically, because many of citations in OMIM refer to studies of genes in species other than human.
      • PubMed (OMIM)
        Links are provided when Gene has a link to a record in OMIM, and OMIM explicitly cites these publications in PubMed.
      • Taxonomy
        Link to related taxonomy entry
      • UniSTS
        Related UniSTS records

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