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HMGB1P8 high mobility group box 1 pseudogene 8 [ Homo sapiens (human) ]

Gene ID: 692147, updated on 23-Nov-2021

Summary

Official Symbol
HMGB1P8provided by HGNC
Official Full Name
high mobility group box 1 pseudogene 8provided by HGNC
Primary source
HGNC:HGNC:13319
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
HMG1L8; HMGB1L8
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Genomic context

See HMGB1P8 in Genome Data Viewer
Location:
15q26.1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 15 NC_000015.10 (89135081..89136685, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (89678312..89679916, complement)

Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene coronary artery disease region linked MFGE8 regulatory lncRNA Neighboring gene abhydrolase domain containing 2, acylglycerol lipase Neighboring gene RNA, U7 small nuclear 195 pseudogene Neighboring gene vesicle-associated membrane protein-associated protein A pseudogene Neighboring gene retinaldehyde binding protein 1

Genomic regions, transcripts, and products

General gene information

Other Names

  • high-mobility group (nonhistone chromosomal) protein 1-like 8
  • high-mobility group box 1-like 8

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_005579.5 

    Range
    101..1705
    Download
    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_000015.10 Reference GRCh38.p13 Primary Assembly

    Range
    89135081..89136685 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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