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    LCN1P2 lipocalin 1 pseudogene 2 [ Homo sapiens (human) ]

    Gene ID: 653163, updated on 4-May-2015
    Official Symbol
    LCN1P2provided by HGNC
    Official Full Name
    lipocalin 1 pseudogene 2provided by HGNC
    Primary source
    HGNC:HGNC:23680
    Gene type
    pseudo
    RefSeq status
    INFERRED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    LCN1L2; bA244N20.11
    See LCN1P2 in Epigenomics, MapViewer
    Location:
    9q34.2
    Annotation release Status Assembly Chr Location
    107 current GRCh38.p2 (GCF_000001405.28) 9 NC_000009.12 (133317505..133318569)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (136184440..136185304)

    Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene odorant binding protein 2B Neighboring gene lipocalin 1 pseudogene 1 Neighboring gene ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase; transferase B, alpha 1-3-galactosyltransferase) Neighboring gene surfeit 6 Neighboring gene ribosomal protein L21 pseudogene 81

    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_009693.2 

      Range
      101..1165
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 107

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

    Reference GRCh38.p2 Primary Assembly

    Genomic

    1. NC_000009.12 Reference GRCh38.p2 Primary Assembly

      Range
      133317505..133318569
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Reference GRCh38.p2 PATCHES

    Genomic

    1. NW_009646201.1 Reference GRCh38.p2 PATCHES

      Range
      143599..144663
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate CHM1_1.1

    Genomic

    1. NC_018920.2 Alternate CHM1_1.1

      Range
      136334541..136335604
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)