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    SLC2A13P1 SLC2A13 pseudogene 1 [ Homo sapiens (human) ]

    Gene ID: 106480239, updated on 10-Oct-2023

    Summary

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    Official Symbol
    SLC2A13P1provided by HGNC
    Official Full Name
    SLC2A13 pseudogene 1provided by HGNC
    Primary source
    HGNC:HGNC:48929
    See related
    Ensembl:ENSG00000254954 AllianceGenome:HGNC:48929
    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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    Location:
    8q12.1
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (60141821..60142142)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (60565853..60566174)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (61054380..61054701)

    Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105375861 Neighboring gene MPRA-validated peak7046 silencer Neighboring gene H3K27ac hESC enhancer GRCh37_chr8:61042587-61043088 Neighboring gene uncharacterized LOC105375863 Neighboring gene carbonic anhydrase 8 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:61193435-61193941 Neighboring gene ReSE screen-validated silencer GRCh37_chr8:61193934-61194142 Neighboring gene CRISPRi-validated cis-regulatory element chr8.1767 Neighboring gene uncharacterized LOC105375864 Neighboring gene CRISPRi-validated cis-regulatory element chr8.1768 Neighboring gene CRISPRi-validated cis-regulatory element chr8.1769

    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)

    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_043800.1 

      Range
      101..422
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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_000008.11 Reference GRCh38.p14 Primary Assembly

      Range
      60141821..60142142
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060932.1 Alternate T2T-CHM13v2.0

      Range
      60565853..60566174
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

    Gene LinkOut

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    Molecular Biology Databases