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PRELID1P6 PRELID1 pseudogene 6 [ Homo sapiens (human) ]

Gene ID: 388955, updated on 25-Jan-2022

Summary

Official Symbol
PRELID1P6provided by HGNC
Official Full Name
PRELID1 pseudogene 6provided by HGNC
Primary source
HGNC:HGNC:54771
See related
AllianceGenome:HGNC:54771
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 PRELID1P6 in Genome Data Viewer
Location:
2p15
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 2 NC_000002.12 (63622084..63623009, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (63849218..63850143, complement)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene WD repeat containing planar cell polarity effector Neighboring gene MTFR2 pseudogene 1 Neighboring gene malate dehydrogenase 1 Neighboring gene ribosomal protein S4X pseudogene 5 Neighboring gene ribosomal protein L27 pseudogene 6

Genomic regions, transcripts, and products

General gene information

Other Names

  • PRELI domain containing 1 pseudogene
  • PRELI domain-containing protein 1, mitochondrial pseudogene
  • PX19 protein 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_022937.3 

    Range
    101..1026
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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_000002.12 Reference GRCh38.p13 Primary Assembly

    Range
    63622084..63623009 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NR_003131.1: Suppressed sequence

    Description
    NR_003131.1: This RefSeq was permanently suppressed because there is insufficient evidence that this locus is transcribed.
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