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    ARSLP1 arylsulfatase L pseudogene 1 [ Homo sapiens (human) ]

    Gene ID: 10033, updated on 10-Oct-2023

    Summary

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    Official Symbol
    ARSLP1provided by HGNC
    Official Full Name
    arylsulfatase L pseudogene 1provided by HGNC
    Primary source
    HGNC:HGNC:720
    See related
    AllianceGenome:HGNC:720
    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
    ARSEP; ARSEP1
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    Genomic context

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    Location:
    Yq11.21
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) Y NC_000024.10 (12332071..12347692)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) Y NC_060948.1 (13239509..13255124)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (14452798..14468423)

    Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene RNA, 7SL, cytoplasmic 702, pseudogene Neighboring gene AZFa HERV15yq1 recombination region Neighboring gene family with sequence similarity 8, member A1 pseudogene Neighboring gene uncharacterized LOC107987343 Neighboring gene arylsulfatase D pseudogene 1 Neighboring gene glycogenin 2 pseudogene 1

    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. Characterization of a cluster of sulfatase genes on Xp22.3 suggests gene duplications in an ancestral pseudoautosomal region. Meroni G, et al. Hum Mol Genet, 1996 Apr. PMID 8845834
    2. The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes. Skaletsky H, et al. Nature, 2003 Jun 19. PMID 12815422

    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)

    See Variation Viewer (GRCh38)

    General gene information

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    Markers

    Other Names

    • arylsulfatase E (chondrodysplasia punctata 1) pseudogene
    • arylsulfatase E pseudogene 1

    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_000880.5 

      Range
      14..15635
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      GenBank, FASTA, Sequence Viewer (Graphics)

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000024.10 Reference GRCh38.p14 Primary Assembly

      Range
      12332071..12347692
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060948.1 Alternate T2T-CHM13v2.0

      Range
      13239509..13255124
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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