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PIMREGP2 PIMREG pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 402182, updated on 23-Nov-2021

Summary

Official Symbol
PIMREGP2provided by HGNC
Official Full Name
PIMREG pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:54613
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

See PIMREGP2 in Genome Data Viewer
Location:
4q24
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 4 NC_000004.12 (105525957..105527459, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (106447114..106448616, complement)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene inorganic pyrophosphatase 2 Neighboring gene RNA, U6 small nuclear 553, pseudogene Neighboring gene eukaryotic translation elongation factor 1 alpha 1 pseudogene 9 Neighboring gene uncharacterized LOC105377352 Neighboring gene ATP synthase F1 subunit epsilon pseudogene 1

Genomic regions, transcripts, and products

General gene information

Other Names

  • PICALM interacting mitotic regulator pseudogene
  • family with sequence similarity 64 member A pseudogene

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_022022.3 

    Range
    101..1603
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000004.12 Reference GRCh38.p13 Primary Assembly

    Range
    105525957..105527459 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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