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    SMCR6 Smith-Magenis syndrome chromosome region, candidate 6 [ Homo sapiens (human) ]

    Gene ID: 140772, updated on 24-Jul-2021

    Summary

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    Gene symbol
    SMCR6
    Gene description
    Smith-Magenis syndrome chromosome region, candidate 6
    Gene type
    ncRNA
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Annotation information
    not in current annotation release
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    Genomic context

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    Location:
    chromosome: 17

    Bibliography

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    Related articles in PubMed

    1. Genes in a refined Smith-Magenis syndrome critical deletion interval on chromosome 17p11.2 and the syntenic region of the mouse. Bi W, et al. Genome Res, 2002 May. PMID 11997338, Free PMC Article

    GeneRIFs: Gene References Into Functions

    General gene information

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    Other Names

    • Smith-Magenis syndrome chromosome region, candidate 6 (non-protein coding)

    Clone Names

    • DKFZp686J19223
    Nucleotide Protein
    Heading Accession and Version

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