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    PRMT5P1 protein arginine methyltransferase 5 pseudogene 1 [ Homo sapiens (human) ]

    Gene ID: 100420927, updated on 17-Sep-2024

    Summary

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    Official Symbol
    PRMT5P1provided by HGNC
    Official Full Name
    protein arginine methyltransferase 5 pseudogene 1provided by HGNC
    Primary source
    HGNC:HGNC:32524
    See related
    AllianceGenome:HGNC:32524
    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 PRMT5P1 in Genome Data Viewer
    Location:
    4q31.22
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (147458527..147459326, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (150782649..150783448, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (148379679..148380478, complement)

    Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene microRNA 548g Neighboring gene ribosomal protein L31 pseudogene 26 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr4:148381637-148382836 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 21998 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 21999 Neighboring gene endothelin receptor type A Neighboring gene general transcription factor IIF subunit 2 pseudogene 1 Neighboring gene uncharacterized LOC124900795

    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)

    See Variation Viewer (GRCh38)

    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_025173.2 

      Range
      101..900
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      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_000004.12 Reference GRCh38.p14 Primary Assembly

      Range
      147458527..147459326 complement
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      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060928.1 Alternate T2T-CHM13v2.0

      Range
      150782649..150783448 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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