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FTH1P21 ferritin heavy chain 1 pseudogene 21 [ Homo sapiens (human) ]

Gene ID: 2510, updated on 4-Mar-2025

Summary

Official Symbol
FTH1P21provided by HGNC
Official Full Name
ferritin heavy chain 1 pseudogene 21provided by HGNC
Primary source
HGNC:HGNC:3997
See related
AllianceGenome:HGNC:3997
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
FTHP2; FTHL21
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Genomic context

See FTH1P21 in Genome Data Viewer
Location:
4q32.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (156006256..156007180)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (159351682..159352607)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (156927408..156928332)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene tryptophan 2,3-dioxygenase Neighboring gene Sharpr-MPRA regulatory region 9973 Neighboring gene cathepsin O Neighboring gene H3K27ac hESC enhancer GRCh37_chr4:157027553-157028054 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr4:157032791-157033399 Neighboring gene uncharacterized LOC102724785 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 15771 Neighboring gene MPRA-validated peak5138 silencer Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_74949 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:157210831-157211442 Neighboring gene uncharacterized LOC105377508

Genomic regions, transcripts, and products

General gene information

Other Names

  • ferritin, heavy polypeptide 1 pseudogene 21
  • ferritin, heavy polypeptide pseudogene 2
  • ferritin, heavy polypeptide-like 21

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_001121.4 

    Range
    101..1025
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

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_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    156006256..156007180
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    159351682..159352607
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)