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    FTHL18P ferritin heavy chain like 18, pseudogene [ Homo sapiens (human) ]

    Gene ID: 441490, updated on 10-Dec-2024

    Summary

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    Official Symbol
    FTHL18Pprovided by HGNC
    Official Full Name
    ferritin heavy chain like 18, pseudogeneprovided by HGNC
    Primary source
    HGNC:HGNC:3988
    See related
    Ensembl:ENSG00000300194 AllianceGenome:HGNC:3988
    Gene type
    pseudo
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    FTHL18; FTH1P18
    Orthologs
    all
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    Genomic context

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    See FTHL18P in Genome Data Viewer
    Location:
    Xp21.1
    Exon count:
    1
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (37042875..37043792, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (36638655..36639572, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (37060948..37061865, complement)

    Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene LanC like family member 3 pseudogene Neighboring gene family with sequence similarity 47 member C Neighboring gene ferritin heavy chain 1 pseudogene 29 Neighboring gene MOB kinase activator 1A pseudogene 2

    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. Initial assessment of human gene diversity and expression patterns based upon 83 million nucleotides of cDNA sequence. Adams MD, et al. Nature, 1995 Sep 28. PMID 7566098

    GeneRIFs: Gene References Into Functions

    Phenotypes

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    Find tests for this gene in the NIH Genetic Testing Registry (GTR)

    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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    Homology

    Other Names

    • ferritin heavy chain 1 pseudogene 18
    • ferritin heavy chain like 18
    • ferritin, heavy polypeptide 1 pseudogene 18
    • ferritin, heavy polypeptide-like 18

    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_171164.1 RNA Sequence

      Status: VALIDATED

      Source sequence(s)
      BX842568
      Related
      ENST00000769915.1

    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_000023.11 Reference GRCh38.p14 Primary Assembly

      Range
      37042875..37043792 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060947.1 Alternate T2T-CHM13v2.0

      Range
      36638655..36639572 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NG_008265.1: Suppressed sequence

      Description
      NG_008265.1: This RefSeq was permanently suppressed because it is now thought that this gene does encode a protein.

    2. NM_001271682.2: Suppressed sequence

      Description
      NM_001271682.2: This RefSeq was removed because it is now thought that this gene does not encode a protein.
    Nucleotide Protein
    Heading Accession and Version

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