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    LOC100507412 uncharacterized LOC100507412 [ Homo sapiens (human) ]

    Gene ID: 100507412, updated on 10-Oct-2023

    Summary

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    Gene symbol
    LOC100507412
    Gene description
    uncharacterized LOC100507412
    Gene type
    ncRNA
    RefSeq status
    VALIDATED
    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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    Location:
    chromosome: 15
    Exon count:
    7
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) Unplaced Scaffold NT_167214.1 (97129..126696)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 15 NC_060939.1 (2502018..2530822)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) Unplaced Scaffold NT_167214.1 (97129..126696)

    NT_167214.1Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC100507395 Neighboring gene vomeronasal 1 receptor 112 pseudogene Neighboring gene RNA, 45S pre-ribosomal N5 Neighboring gene RNA, 18S ribosomal N5 Neighboring gene RNA, 5.8S ribosomal N5 Neighboring gene RNA, 28S ribosomal N5 Neighboring gene cell division cycle 27 homolog pseudogene Neighboring gene origin of replication in ribosomal DNA intergenic spacer Neighboring gene RNA, 18S ribosomal pseudogene 3

    NW_021160018.1Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124905531 Neighboring gene C-terminal-binding protein 2-like

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Bibliography

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    Related articles in PubMed

    1. Complete sequencing and characterization of 21,243 full-length human cDNAs. Ota T, et al. Nat Genet, 2004 Jan. PMID 14702039

    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)

    See Variation Viewer (GRCh38)

    Genotypes

    General gene information

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    Markers

    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.

    RNA

    1. NR_038958.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL592188

    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. NT_167214.1 Reference GRCh38.p14 Primary Assembly

      Range
      97129..126696
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Reference GRCh38.p14 PATCHES

    Genomic

    1. NW_021160018.1 Reference GRCh38.p14 PATCHES

      Range
      990..4420 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060939.1 Alternate T2T-CHM13v2.0

      Range
      2502018..2530822
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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