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

Gene ID: 441490, updated on 11-Jun-2021

Summary

Official Symbol
FTHL18Pprovided by HGNC
Official Full Name
ferritin heavy chain like 18, pseudogeneprovided by HGNC
Primary source
HGNC: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
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Genomic context

See FTHL18P in Genome Data Viewer
Location:
Xp21.1
Exon count:
1
Annotation release Status Assembly Chr Location
109.20210514 current GRCh38.p13 (GCF_000001405.39) X NC_000023.11 (37042875..37043792, complement)
105.20201022 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 3 pseudogene Neighboring gene family with sequence similarity 47 member C Neighboring gene ferritin, heavy polypeptide-like 17 pseudogene Neighboring gene MOB kinase activator 1A pseudogene 2

Genomic regions, transcripts, and products

General gene information

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

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20210514

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000023.11 Reference GRCh38.p13 Primary Assembly

    Range
    37042875..37043792 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.
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