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HMGB1P4 high mobility group box 1 pseudogene 4 [ Homo sapiens (human) ]

Gene ID: 10355, updated on 11-Jun-2021

Summary

Official Symbol
HMGB1P4provided by HGNC
Official Full Name
high mobility group box 1 pseudogene 4provided by HGNC
Primary source
HGNC:HGNC:4996
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
HMG1L4; HMG1L4P; HMGB1L4
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Genomic context

See HMGB1P4 in Genome Data Viewer
Location:
2q31.1
Annotation release Status Assembly Chr Location
109.20210514 current GRCh38.p13 (GCF_000001405.39) 2 NC_000002.12 (170600138..170602384, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (171456648..171458894, complement)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene myosin IIIB Neighboring gene Sharpr-MPRA regulatory region 12446 Neighboring gene MYO3B antisense RNA 1 Neighboring gene uncharacterized LOC100130256 Neighboring gene ERICH2 divergent transcript Neighboring gene long intergenic non-protein coding RNA 1124

Genomic regions, transcripts, and products

General gene information

Other Names

  • high-mobility group (nonhistone chromosomal) protein 1-like 4 pseudogene
  • high-mobility group box 1-like 4

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_004767.4 

    Range
    101..2347
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20210514

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
    170600138..170602384 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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