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    MYCNOS MYCN opposite strand [ Homo sapiens (human) ]

    Gene ID: 10408, updated on 10-Dec-2024

    Summary

    Official Symbol
    MYCNOSprovided by HGNC
    Official Full Name
    MYCN opposite strandprovided by HGNC
    Primary source
    HGNC:HGNC:16911
    See related
    Ensembl:ENSG00000233718 MIM:605374; AllianceGenome:HGNC:16911
    Gene type
    ncRNA
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    NCYM; NYCM; N-CYM; MYCN-AS1
    Summary
    This gene is transcribed in antisense to the v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog gene (MYCN). It is thought to encode a small, novel protein that stabilizes MYCN, prevents apoptosis, and promotes cell proliferation. Transcripts at this locus may also act directly as functional RNAs to recruit transcriptional regulators to the promoter of MYCN and stimulate transcription of this oncogene. This gene therefore functions through both RNA and protein products. [provided by RefSeq, Aug 2016]
    Expression
    Low expression observed in reference dataset See more
    Orthologs
    NEW
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    Genomic context

    See MYCNOS in Genome Data Viewer
    Location:
    2p24.3
    Exon count:
    6
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (15936265..15942433, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (15967896..15974065, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (16076387..16082555, complement)

    Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene small nucleolar RNA U13 Neighboring gene MYCN upstream transcript Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr2:16078668-16079225 Neighboring gene H3K27ac hESC enhancer GRCh37_chr2:16080270-16080800 Neighboring gene RNA, 7SL, cytoplasmic 104, pseudogene Neighboring gene MYCN proto-oncogene, bHLH transcription factor Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr2:16120447-16121234 Neighboring gene ReSE screen-validated silencer GRCh37_chr2:16140957-16141151 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:16153570-16154181 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr2:16174407-16174907 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 15348 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr2:16197762-16198262 Neighboring gene gastric cancer associated transcript 3

    Genomic regions, transcripts, and products

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    General gene information

    Markers

    Other Names

    • DNA-binding transcriptional activator NCYM
    • MYCN antisense RNA 1
    • MYCN opposite strand/antisense RNA (non-protein coding)
    • N-myc opposite strand
    • v-myc myelocytomatosis viral related oncogene, neuroblastoma derived opposite strand

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    Process Evidence Code Pubs
    involved_in negative regulation of kinase activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in regulation of protein stability IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    Component Evidence Code Pubs
    located_in cytoplasm IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in nucleus IDA
    Inferred from Direct Assay
    more info
    PubMed 

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    RefSeqs maintained independently of Annotated Genomes

    These reference sequences exist independently of genome builds. Explain

    These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

    RNA

    1. NR_110230.2 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC010145
      Related
      ENST00000641263.1
    2. NR_161162.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC010145, KF456635
    3. NR_161163.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AC010145, KF456635
      Related
      ENST00000641534.2

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000002.12 Reference GRCh38.p14 Primary Assembly

      Range
      15936265..15942433 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060926.1 Alternate T2T-CHM13v2.0

      Range
      15967896..15974065 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)