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    SFPQP1 splicing factor proline and glutamine rich pseudogene 1 [ Homo sapiens (human) ]

    Gene ID: 23758, updated on 10-Oct-2023

    Summary

    Official Symbol
    SFPQP1provided by HGNC
    Official Full Name
    splicing factor proline and glutamine rich pseudogene 1provided by HGNC
    Primary source
    HGNC:HGNC:10775
    See related
    AllianceGenome:HGNC:10775
    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
    SFPQP
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    Genomic context

    Location:
    Yq11.221
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) Y NC_000024.10 (13094804..13097725)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) Y NC_060948.1 (14003076..14005997)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (15206718..15209639)

    Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene DEAD-box helicase 3 Y-linked Neighboring gene calcium/calmodulin dependent serine protein kinase pseudogene 1 Neighboring gene uncharacterized LOC112268312 Neighboring gene AZFa HERV15yq2 recombination region Neighboring gene TGF-beta activated kinase 1/MAP3K7 binding protein 3 pseudogene 1

    Genomic regions, transcripts, and products

    General gene information

    Other Names

    • splicing factor proline/glutamine rich (polypyrimidine tract binding protein associated) pseudogene
    • splicing factor proline/glutamine-rich (polypyrimidine tract binding protein associated) pseudogene 1
    • splicing factor proline/glutamine-rich pseudogene 1

    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_002816.4 

      Range
      101..3022
      Download
      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_000024.10 Reference GRCh38.p14 Primary Assembly

      Range
      13094804..13097725
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060948.1 Alternate T2T-CHM13v2.0

      Range
      14003076..14005997
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)