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HMGB1P39 high mobility group box 1 pseudogene 39 [ Homo sapiens (human) ]

Gene ID: 100419972, updated on 23-Nov-2021

Summary

Official Symbol
HMGB1P39provided by HGNC
Official Full Name
high mobility group box 1 pseudogene 39provided by HGNC
Primary source
HGNC:HGNC:39186
See related
Ensembl:ENSG00000203489
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 HMGB1P39 in Genome Data Viewer
Location:
6q14.1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 6 NC_000006.12 (75319032..75319980, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (76028748..76029696, complement)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene transmembrane protein 30A Neighboring gene TMEM30A divergent transcript Neighboring gene filamin A interacting protein 1 Neighboring gene uncharacterized LOC101928540 Neighboring gene microRNA 4463 Neighboring gene UBE2V1 pseudogene 15

Genomic regions, transcripts, and products

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_025834.1 

    Range
    101..1049
    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_000006.12 Reference GRCh38.p13 Primary Assembly

    Range
    75319032..75319980 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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