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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
    Download
    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
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    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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