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    FTH1P4 ferritin heavy chain 1 pseudogene 4 [ Homo sapiens (human) ]

    Gene ID: 2499, updated on 17-Jun-2019

    Summary

    Official Symbol
    FTH1P4provided by HGNC
    Official Full Name
    ferritin heavy chain 1 pseudogene 4provided by HGNC
    Primary source
    HGNC:HGNC:3991
    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
    FTHL4

    Genomic context

    See FTH1P4 in Genome Data Viewer
    Location:
    3q21.3
    Annotation release Status Assembly Chr Location
    109.20190607 current GRCh38.p13 (GCF_000001405.39) 3 NC_000003.12 (128764306..128765217, complement)
    105 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (128483149..128484064, complement)

    Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene POU class 5 homeobox 1 pseudogene 6 Neighboring gene RAB7A, member RAS oncogene family Neighboring gene microtubule affinity regulating kinase 2 pseudogene 8 Neighboring gene RNA, 7SL, cytoplasmic 698, pseudogene Neighboring gene ribosomal protein S15a pseudogene 16

    Genomic regions, transcripts, and products

    Bibliography

    Related articles in PubMed

    GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

    General gene information

    Other Names

    • ferritin, heavy polypeptide 1 pseudogene 4
    • ferritin, heavy polypeptide-like 4 pseudogene

    NCBI Reference Sequences (RefSeq)

    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_004769.6 

      Range
      101..1012
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh38.p13 Primary Assembly

    Genomic

    1. NC_000003.12 Reference GRCh38.p13 Primary Assembly

      Range
      128764306..128765217 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
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