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HMGN2P12 high mobility group nucleosomal binding domain 2 pseudogene 12 [ Homo sapiens (human) ]

Gene ID: 3153, updated on 17-Sep-2024

Summary

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Official Symbol
HMGN2P12provided by HGNC
Official Full Name
high mobility group nucleosomal binding domain 2 pseudogene 12provided by HGNC
Primary source
HGNC:HGNC:4991
See related
AllianceGenome:HGNC:4991
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
60H; HMG17P2; HMGN2L12
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Genomic context

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See HMGN2P12 in Genome Data Viewer
Location:
6q21
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (106930969..106932128, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (108107060..108108219, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 6 (PATCHES) NW_004504300.1 (235592..236751, complement)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124901552 Neighboring gene uncharacterized LOC105377928 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 24897 Neighboring gene trafficking protein particle complex subunit 6A-like Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 17434 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 17435 Neighboring gene CD24 molecule

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. Retropseudogenes for human chromosomal protein HMG-17. Srikantha T, et al. J Mol Biol, 1987 Oct 5. PMID 3441004

GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

General gene information

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Markers

Other Names

  • high-mobility group (nonhistone chromosomal) protein 17 pseudogene 2

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_001142.4 

    Range
    101..1260
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    106930969..106932128 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    108107060..108108219 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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