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H2AL1QP H2A.L variant histone 1Q, pseudogene [ Homo sapiens (human) ]

Gene ID: 115482714, updated on 17-Jun-2021

Summary

Official Symbol
H2AL1QPprovided by HGNC
Official Full Name
H2A.L variant histone 1Q, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:53959
See related
Ensembl:ENSG00000249467
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
H2A.L.1
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Genomic context

See H2AL1QP in Genome Data Viewer
Location:
Xp21.1
Annotation release Status Assembly Chr Location
109.20210514 current GRCh38.p13 (GCF_000001405.39) X NC_000023.11 (36719918..36720221)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (36737991..36738294)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene cilia and flagella associated protein 47 Neighboring gene high mobility group box 1 pseudogene 16 Neighboring gene uncharacterized LOC101928627 Neighboring gene ribosomal protein S15a pseudogene 40 Neighboring gene uncharacterized LOC105373155 Neighboring gene myosin heavy chain IB Neighboring gene TFDP1 pseudogene 2

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_066059.1 

    Range
    101..404
    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_000023.11 Reference GRCh38.p13 Primary Assembly

    Range
    36719918..36720221
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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