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FTH1P2 ferritin heavy chain 1 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 2497, updated on 8-Nov-2023

Summary

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Official Symbol
FTH1P2provided by HGNC
Official Full Name
ferritin heavy chain 1 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:3989
See related
Ensembl:ENSG00000234975 AllianceGenome:HGNC:3989
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
FTHL2
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Genomic context

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Location:
1q42.13
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (228687417..228687879)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (228065316..228065778)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (228823164..228823626)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124900442 Neighboring gene RNA, 5S ribosomal pseudogene 18 Neighboring gene dual specificity phosphatase 5 pseudogene 1 Neighboring gene ras homolog family member U Neighboring gene H3K27ac hESC enhancer GRCh37_chr1:228817664-228818164 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:228890621-228891178 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:228891179-228891735 Neighboring gene eukaryotic translation elongation factor 1 alpha 2 pseudogene Neighboring gene ReSE screen-validated silencer GRCh37_chr1:228947507-228947724 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1924 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr1:228984653-228985467 Neighboring gene MPRA-validated peak749 silencer Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:229001855-229002525 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:229003867-229004535 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 2698 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:229035335-229035990 Neighboring gene Sharpr-MPRA regulatory region 14212 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:229054689-229055189 Neighboring gene uncharacterized LOC124904539 Neighboring gene uncharacterized LOC105373143

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. Conserved mutations in human ferritin H pseudogenes: a second functional sequence or an evolutionary quirk? Zheng H, et al. Biochim Biophys Acta, 1997 Mar 20. PMID 9116028
  2. Genes for the 'H' subunit of human ferritin are present on a number of human chromosomes. Cragg SJ, et al. Hum Genet, 1985. PMID 3862645

GeneRIFs: Gene References Into Functions

Phenotypes

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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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Other Names

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

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_007330.2 

    Range
    101..563
    Download
    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_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    228687417..228687879
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 PATCHES

Genomic

  1. NW_018654708.1 Reference GRCh38.p14 PATCHES

    Range
    264419..264881
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    228065316..228065778
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NR_002200.1: Suppressed sequence

    Description
    NR_002200.1: This RefSeq was permanently suppressed because it is now thought that this pseudogene is not transcribed.
Nucleotide Protein
Heading Accession and Version

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