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FTH1P7 ferritin heavy chain 1 pseudogene 7 [ Homo sapiens (human) ]

Gene ID: 2500, updated on 10-Oct-2023

Summary

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Official Symbol
FTH1P7provided by HGNC
Official Full Name
ferritin heavy chain 1 pseudogene 7provided by HGNC
Primary source
HGNC:HGNC:3994
See related
AllianceGenome:HGNC:3994
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
FTHL7
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Genomic context

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Location:
13q12.12
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (22695862..22696783, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (21893932..21894853, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (23270001..23270922, complement)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107984599 Neighboring gene Sharpr-MPRA regulatory region 8838 Neighboring gene uncharacterized LOC124903133 Neighboring gene Sharpr-MPRA regulatory region 3351 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr13:23126652-23127851 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr13:23218322-23218822 Neighboring gene DEAD-box helicase 39A pseudogene 1 Neighboring gene uncharacterized LOC124903254

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 7
  • ferritin, heavy polypeptide-like 7

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_007331.3 

    Range
    101..1022
    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_000013.11 Reference GRCh38.p14 Primary Assembly

    Range
    22695862..22696783 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    21893932..21894853 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NR_002202.2: Suppressed sequence

    Description
    NR_002202.2: 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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