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HMGB1P44 high mobility group box 1 pseudogene 44 [ Homo sapiens (human) ]

Gene ID: 100130279, updated on 13-May-2022

Summary

Official Symbol
HMGB1P44provided by HGNC
Official Full Name
high mobility group box 1 pseudogene 44provided by HGNC
Primary source
HGNC:HGNC:39275
See related
Ensembl:ENSG00000248956 AllianceGenome:HGNC:39275
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 HMGB1P44 in Genome Data Viewer
Location:
4q21.1
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (77963940..77964530)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (81304765..81305355)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (78885094..78885684)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC102724916 Neighboring gene mitochondrial ribosomal protein L1 Neighboring gene serine and arginine rich splicing factor 10 pseudogene Neighboring gene heterogeneous nuclear ribonucleoprotein A1 pseudogene 56 Neighboring gene uncharacterized LOC107986293 Neighboring gene Fraser extracellular matrix complex subunit 1

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_022063.1 

    Range
    101..691
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    77963940..77964530
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    81304765..81305355
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)