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    LOC100533622 sulfite oxidase pseudogene [ Homo sapiens (human) ]

    Gene ID: 100533622, updated on 17-Sep-2024

    Summary

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    Gene symbol
    LOC100533622
    Gene description
    sulfite oxidase pseudogene
    See related
    Ensembl:ENSG00000253423
    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

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    See LOC100533622 in Genome Data Viewer
    Location:
    8q21.13
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (83200952..83202431, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (83632683..83634162, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (84113187..84114666, complement)

    Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene DPPA3 pseudogene 9 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr8:83976499-83977295 Neighboring gene solute carrier family 25 member 43 pseudogene Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27587 Neighboring gene NANOG hESC enhancer GRCh37_chr8:84272719-84273222 Neighboring gene long intergenic non-protein coding RNA 1419 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr8:84416975-84417517 Neighboring gene NANOG hESC enhancer GRCh37_chr8:84418651-84419152 Neighboring gene origin of replication S14 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr8:84457496-84458695 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr8:84489861-84491060 Neighboring gene uncharacterized LOC105375932

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Bibliography

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    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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    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_028882.1 

      Range
      101..1580
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      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_000008.11 Reference GRCh38.p14 Primary Assembly

      Range
      83200952..83202431 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060932.1 Alternate T2T-CHM13v2.0

      Range
      83632683..83634162 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

    Gene LinkOut

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