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FTH1P14 ferritin heavy chain 1 pseudogene 14 [ Homo sapiens (human) ]

Gene ID: 139431, updated on 10-Oct-2023

Summary

Official Symbol
FTH1P14provided by HGNC
Official Full Name
ferritin heavy chain 1 pseudogene 14provided by HGNC
Primary source
HGNC:HGNC:39090
See related
AllianceGenome:HGNC:39090
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

Location:
Xp21.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (34147040..34147753)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (33745132..33745845)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (34165157..34165870)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105373153 Neighboring gene H3K4me1 hESC enhancer GRCh37_chrX:33835505-33836004 Neighboring gene H3K4me1 hESC enhancer GRCh37_chrX:33847535-33848036 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chrX:33926163-33926715 Neighboring gene H3K4me1 hESC enhancer GRCh37_chrX:33987093-33987592 Neighboring gene H3K4me1 hESC enhancer GRCh37_chrX:34165078-34165618 Neighboring gene ReSE screen-validated silencer GRCh37_chrX:34165632-34165795 Neighboring gene H3K4me1 hESC enhancer GRCh37_chrX:34175554-34176054 Neighboring gene family with sequence similarity 47 member A Neighboring gene uncharacterized LOC107985674 Neighboring gene SRSF2 pseudogene 1

Genomic regions, transcripts, and products

General gene information

Other Names

  • ferritin, heavy polypeptide 1 pseudogene 14
  • ferritin, heavy polypeptide-like 17 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_023176.3 

    Range
    101..814
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    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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    34147040..34147753
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    33745132..33745845
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)