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    LOC283788 FSHD region gene 1 pseudogene [ Homo sapiens (human) ]

    Gene ID: 283788, updated on 17-Sep-2024

    Summary

    Gene symbol
    LOC283788
    Gene description
    FSHD region gene 1 pseudogene
    Gene type
    pseudo
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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    Genomic context

    See LOC283788 in Genome Data Viewer
    Location:
    chromosome: 21
    Exon count:
    7
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) Unplaced Scaffold NT_167213.1 (56349..99642, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 21 NC_060945.1 (2585669..2628967, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) Unplaced Scaffold NT_167213.1 (56349..99642, complement)

    NT_167213.1Genomic Context describing neighboring genes Neighboring gene angiogenic factor with G patch and FHA domains 1-like Neighboring gene uncharacterized LOC105379420

    Genomic regions, transcripts, and products

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Clone Names

    • FLJ16488, FLJ31053, FLJ45377, FLJ90087, FLJ97977

    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.

    RNA

    1. NR_027436.2 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      AL592183

    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. NT_167213.1 Reference GRCh38.p14 Primary Assembly

      Range
      56349..99642 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060945.1 Alternate T2T-CHM13v2.0

      Range
      2585669..2628967 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)