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FTH1P5 ferritin heavy chain 1 pseudogene 5 [ Homo sapiens (human) ]

Gene ID: 2509, updated on 10-Oct-2023

Summary

Official Symbol
FTH1P5provided by HGNC
Official Full Name
ferritin heavy chain 1 pseudogene 5provided by HGNC
Primary source
HGNC:HGNC:3996
See related
AllianceGenome:HGNC:3996
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
FTHL5; FTHP1
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Genomic context

See FTH1P5 in Genome Data Viewer
Location:
6p12.3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (50912550..50913462, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (50755297..50756209, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (50880263..50881175, complement)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene ribosomal protein S17 pseudogene 5 Neighboring gene TNPO3 pseudogene 2 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr6:50992467-50993666 Neighboring gene MPRA-validated peak5848 silencer Neighboring gene VISTA enhancer hs217 Neighboring gene NANOG hESC enhancer GRCh37_chr6:51203839-51204355 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr6:51204447-51204975 Neighboring gene MPRA-validated peak5850 silencer Neighboring gene MPRA-validated peak5851 silencer Neighboring gene uncharacterized LOC105375085 Neighboring gene TIAL1 pseudogene

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • ferritin, heavy polypeptide 1 pseudogene 5
  • ferritin, heavy polypeptide pseudogene 1
  • ferritin, heavy polypeptide-like 5

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_005639.3 

    Range
    101..1013
    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_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    50912550..50913462 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    50755297..50756209 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)