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FTH1P8 ferritin heavy chain 1 pseudogene 8 [ Homo sapiens (human) ]

Gene ID: 2501, updated on 13-May-2022

Summary

Official Symbol
FTH1P8provided by HGNC
Official Full Name
ferritin heavy chain 1 pseudogene 8provided by HGNC
Primary source
HGNC:HGNC:3995
See related
AllianceGenome:HGNC:3995
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
FTHL8
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Genomic context

See FTH1P8 in Genome Data Viewer
Location:
Xq28
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (148052012..148052923)
110 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (146317540..146318452)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (147133532..147134443)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene origin of replication in 5' region of FMR1 Neighboring gene fragile site, folic acid type, rare, fra(X)(q27.3) A Neighboring gene fragile X messenger ribonucleoprotein 1 Neighboring gene FMR1 neighbor Neighboring gene RNA, 5S ribosomal pseudogene 524 Neighboring gene HAX1 pseudogene 1 Neighboring gene ribosomal protein L7 like 1 pseudogene 11

Genomic regions, transcripts, and products

General gene information

Other Names

  • ferritin, heavy polypeptide 1 pseudogene 8
  • ferritin, heavy polypeptide-like 8

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_007336.2 

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

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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
    148052012..148052923
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    146317540..146318452
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NR_002203.1: Suppressed sequence

    Description
    NR_002203.1: This RefSeq was permanently suppressed because it is now thought that this pseudogene is not transcribed.