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FTH1P10 ferritin heavy chain 1 pseudogene 10 [ Homo sapiens (human) ]

Gene ID: 2502, updated on 16-Jan-2024

Summary

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Official Symbol
FTH1P10provided by HGNC
Official Full Name
ferritin heavy chain 1 pseudogene 10provided by HGNC
Primary source
HGNC:HGNC:3980
See related
Ensembl:ENSG00000293060 AllianceGenome:HGNC:3980
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
FTHL10
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Genomic context

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See FTH1P10 in Genome Data Viewer
Location:
5p15.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 5 NC_000005.10 (17353713..17354631, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 5 NC_060929.1 (17293106..17294024, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 5 NC_000005.9 (17353822..17354740, complement)

Chromosome 5 - NC_000005.10Genomic Context describing neighboring genes Neighboring gene H3K4me1 hESC enhancer GRCh37_chr5:17311529-17312170 Neighboring gene aurora kinase A interacting protein 1 pseudogene Neighboring gene Sharpr-MPRA regulatory region 14736 Neighboring gene RN7SK pseudogene 133 Neighboring gene long intergenic non-protein coding RNA 2111 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:17400895-17401540 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr5:17401541-17402186 Neighboring gene long intergenic non-protein coding RNA 2217 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr5:17415024-17415837 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr5:17415838-17416650

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. Human ferritin genes: chromosomal assignments and polymorphisms. Gatti RA, et al. Am J Hum Genet, 1987 Oct. PMID 2821803, Free PMC Article
  3. 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 10
  • ferritin, heavy polypeptide-like 10

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_003028.3 

    Range
    101..1019
    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_000005.10 Reference GRCh38.p14 Primary Assembly

    Range
    17353713..17354631 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060929.1 Alternate T2T-CHM13v2.0

    Range
    17293106..17294024 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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