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    RNASEH2CP1 ribonuclease H2 subunit C pseudogene 1 [ Homo sapiens (human) ]

    Gene ID: 386608, updated on 17-Sep-2024

    Summary

    Official Symbol
    RNASEH2CP1provided by HGNC
    Official Full Name
    ribonuclease H2 subunit C pseudogene 1provided by HGNC
    Primary source
    HGNC:HGNC:24117
    See related
    AllianceGenome:HGNC:24117
    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
    AYP1p1
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    Genomic context

    See RNASEH2CP1 in Genome Data Viewer
    Location:
    Yp11.2
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) Y NC_000024.10 (2789806..2790439)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) Y NC_060948.1 (2466646..2467279)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (2657847..2658480)

    Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene RNA, U6 small nuclear 1334, pseudogene Neighboring gene SRY promoter region Neighboring gene sex determining region Y Neighboring gene TOMM22 pseudogene 2 Neighboring gene ribosomal protein S4 Y-linked 1

    Genomic regions, transcripts, and products

    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_011584.2 

      Range
      101..734
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    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_000024.10 Reference GRCh38.p14 Primary Assembly

      Range
      2789806..2790439
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060948.1 Alternate T2T-CHM13v2.0

      Range
      2466646..2467279
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NR_002820.2: Suppressed sequence

      Description
      NR_002820.2: This RefSeq was suppressed permanently because there is little evidence that this is transcribed.