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    NUFIP1P1 NUFIP1 pseudogene 1 [ Homo sapiens (human) ]

    Gene ID: 89761, updated on 17-Sep-2024

    Summary

    Official Symbol
    NUFIP1P1provided by HGNC
    Official Full Name
    NUFIP1 pseudogene 1provided by HGNC
    Primary source
    HGNC:HGNC:8058
    See related
    AllianceGenome:HGNC:8058
    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
    NUFIP1P
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    Genomic context

    See NUFIP1P1 in Genome Data Viewer
    Location:
    6q12
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (66091475..66094945, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (67249562..67253034, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (66801368..66804838, complement)

    Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105377838 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_93892 Neighboring gene uncharacterized LOC105377840 Neighboring gene uncharacterized LOC105377839 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_93910 Neighboring gene uncharacterized LOC105377841 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_94052 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr6:66999393-67000291 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_94110 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr6:67340492-67341092 Neighboring gene NANOG hESC enhancer GRCh37_chr6:67397461-67398132 Neighboring gene transcription elongation regulator 1 pseudogene

    Genomic regions, transcripts, and products

    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_001030.2 

      Range
      101..3571
      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_000006.12 Reference GRCh38.p14 Primary Assembly

      Range
      66091475..66094945 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060930.1 Alternate T2T-CHM13v2.0

      Range
      67249562..67253034 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)