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    NXNP1 nucleoredoxin pseudogene 1 [ Homo sapiens (human) ]

    Gene ID: 100130251, updated on 17-Sep-2024

    Summary

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    Official Symbol
    NXNP1provided by HGNC
    Official Full Name
    nucleoredoxin pseudogene 1provided by HGNC
    Primary source
    HGNC:HGNC:50561
    See related
    AllianceGenome:HGNC:50561
    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 NXNP1 in Genome Data Viewer
    Location:
    1q41
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (218843762..218882551, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (218078444..218117243, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (219017104..219055893, complement)

    Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene small nucleolar RNA U3 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr1:218758840-218759340 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr1:218759341-218759841 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr1:218774035-218775234 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:218795207-218795706 Neighboring gene Sharpr-MPRA regulatory region 6480 Neighboring gene uncharacterized LOC105372924 Neighboring gene uncharacterized LOC124904513 Neighboring gene long intergenic non-protein coding RNA 1710

    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_028320.2 

      Range
      79..38868
      Download
      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_000001.11 Reference GRCh38.p14 Primary Assembly

      Range
      218843762..218882551 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060925.1 Alternate T2T-CHM13v2.0

      Range
      218078444..218117243 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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