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FTH1P19 ferritin heavy chain 1 pseudogene 19 [ Homo sapiens (human) ]

Gene ID: 389844, updated on 11-Jun-2021

Summary

Official Symbol
FTH1P19provided by HGNC
Official Full Name
ferritin heavy chain 1 pseudogene 19provided by HGNC
Primary source
HGNC:HGNC:33525
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
FTHL19
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Genomic context

See FTH1P19 in Genome Data Viewer
Location:
Xp21.1
Annotation release Status Assembly Chr Location
109.20210514 current GRCh38.p13 (GCF_000001405.39) X NC_000023.11 (37491957..37492720)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (37351210..37351973)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene MOB kinase activator 1A pseudogene 2 Neighboring gene proline rich and Gla domain 1 Neighboring gene ferritin heavy chain like 17 pseudogene Neighboring gene ferritin heavy chain 1 pseudogene 27 Neighboring gene family with sequence similarity 47 member D, pseudogene

Genomic regions, transcripts, and products

General gene information

Other Names

  • ferritin, heavy polypeptide 1 pseudogene 19
  • ferritin, heavy polypeptide-like 19

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables ferric iron binding IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
enables ferrous iron binding IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
enables ferroxidase activity IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
Process Evidence Code Pubs
involved_in intracellular sequestering of iron ion IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 
involved_in iron ion transport IEA
Inferred from Electronic Annotation
more info
 
Component Evidence Code Pubs
is_active_in cytoplasm IBA
Inferred from Biological aspect of Ancestor
more info
PubMed 

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_009569.2 

    Range
    101..864
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20210514

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000023.11 Reference GRCh38.p13 Primary Assembly

    Range
    37491957..37492720
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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