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

    Gene ID: 2499, updated on 10-Oct-2023

    Summary

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    Official Symbol
    FTH1P4provided by HGNC
    Official Full Name
    ferritin heavy chain 1 pseudogene 4provided by HGNC
    Primary source
    HGNC:HGNC:3991
    See related
    AllianceGenome: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
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    Genomic context

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    Location:
    3q21.3
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (128764306..128765217, complement)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (131508956..131509867, complement)
    105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (128483149..128484060, complement)

    Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene small nucleolar RNA SNORA24 Neighboring gene MPRA-validated peak4821 silencer Neighboring gene ATAC-STARR-seq lymphoblastoid active region 20493 Neighboring gene H3K27ac hESC enhancer GRCh37_chr3:128444909-128445893 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_64587 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 20494 Neighboring gene RAB7A, member RAS oncogene family Neighboring gene MARK2 pseudogene 8 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:128477315-128477814 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:128488901-128489401 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:128500166-128500666 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:128500667-128501167 Neighboring gene RNA, 7SL, cytoplasmic 698, pseudogene Neighboring gene ATAC-STARR-seq lymphoblastoid active region 20495 Neighboring gene ribosomal protein S15a pseudogene 16

    Genomic regions, transcripts, and products

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    Go to nucleotide: Graphics FASTA GenBank

    Bibliography

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    Related articles in PubMed

    1. Genes for the 'H' subunit of human ferritin are present on a number of human chromosomes. Cragg SJ, et al. Hum Genet, 1985. PMID 3862645

    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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    Other Names

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

    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_004769.6 

      Range
      101..1012
      Download
      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_000003.12 Reference GRCh38.p14 Primary Assembly

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

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060927.1 Alternate T2T-CHM13v2.0

      Range
      131508956..131509867 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
    Nucleotide Protein
    Heading Accession and Version

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