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    RN7SL508P RNA, 7SL, cytoplasmic 508, pseudogene [ Homo sapiens (human) ]

    Gene ID: 106481061, updated on 10-Oct-2023

    Summary

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    Official Symbol
    RN7SL508Pprovided by HGNC
    Official Full Name
    RNA, 7SL, cytoplasmic 508, pseudogeneprovided by HGNC
    Primary source
    HGNC:HGNC:46524
    See related
    Ensembl:ENSG00000244112 AllianceGenome:HGNC:46524
    Gene type
    pseudo
    RefSeq status
    INFERRED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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    Genomic context

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    See RN7SL508P in Genome Data Viewer
    Location:
    12q24.23
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (118993857..118994159)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (118981355..118981657)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (119431662..119431964)

    Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105370019 Neighboring gene small nucleolar RNA SNORA38 Neighboring gene uncharacterized LOC105370020 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr12:119423722-119424248 Neighboring gene serine/arginine repetitive matrix 4 Neighboring gene uncharacterized LOC105370022 Neighboring gene NANOG hESC enhancer GRCh37_chr12:119493434-119493935 Neighboring gene MPRA-validated peak1997 silencer Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:119526455-119527045 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:119527046-119527635 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr12:119527912-119528566 Neighboring gene uncharacterized LOC105370021

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Bibliography

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    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Review eQTL and phenotype association data in this region using PheGenI

    Variation

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    See studies and variants in dbVar

    See Variation Viewer (GRCh37.p13)

    General gene information

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    NCBI Reference Sequences (RefSeq)

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    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.

    Genomic

    1. NG_045761.1 

      Range
      101..403
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      GenBank, FASTA, Sequence Viewer (Graphics)

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000012.12 Reference GRCh38.p14 Primary Assembly

      Range
      118993857..118994159
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060936.1 Alternate T2T-CHM13v2.0

      Range
      118981355..118981657
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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