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FTH1P20 ferritin heavy chain 1 pseudogene 20 [ Homo sapiens (human) ]

Gene ID: 729009, updated on 29-Mar-2023

Summary

Official Symbol
FTH1P20provided by HGNC
Official Full Name
ferritin heavy chain 1 pseudogene 20provided by HGNC
Primary source
HGNC:HGNC:37639
See related
AllianceGenome:HGNC:37639
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
FTHL20
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Genomic context

See FTH1P20 in Genome Data Viewer
Location:
2q31.3
Annotation release Status Assembly Chr Location
RS_2023_03 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (180872705..180873565, complement)
RS_2023_03 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (181356151..181356885, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (181737432..181738292, complement)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105373770 Neighboring gene Sharpr-MPRA regulatory region 10987 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr2:181520993-181522192 Neighboring gene uncharacterized LOC105373771 Neighboring gene SWI/SNF complex antagonist associated with prostate cancer 1 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr2:181678325-181679524 Neighboring gene ribosomal protein L27a pseudogene 3 Neighboring gene UBE2E3 divergent transcript Neighboring gene ubiquitin conjugating enzyme E2 E3

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • ferritin, heavy polypeptide 1 pseudogene 20
  • ferritin, heavy polypeptide-like 20

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_023542.2 

    Range
    101..961
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_03

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000002.12 Reference GRCh38.p14 Primary Assembly

    Range
    180872705..180873565 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060926.1 Alternate T2T-CHM13v2.0

    Range
    181356151..181356885 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)