Format

Send to:

Choose Destination

FTH1P16 ferritin heavy chain 1 pseudogene 16 [ Homo sapiens (human) ]

Gene ID: 2508, updated on 25-Jan-2022

Summary

Official Symbol
FTH1P16provided by HGNC
Official Full Name
ferritin heavy chain 1 pseudogene 16provided by HGNC
Primary source
HGNC:HGNC:3986
See related
AllianceGenome:HGNC:3986
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
FTH2; FTHL16
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See FTH1P16 in Genome Data Viewer
Location:
11q14.1
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 11 NC_000011.10 (77734315..77735232, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (77445360..77446277, complement)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene chloride nucleotide-sensitive channel 1A Neighboring gene uncharacterized LOC107984369 Neighboring gene CRISPRi-validated cis-regulatory element chr11.4537 Neighboring gene remodeling and spacing factor 1 Neighboring gene ribosomal protein S20 pseudogene 27 Neighboring gene adipogenesis associated Mth938 domain containing Neighboring gene ribosomal protein L21 pseudogene 95

Genomic regions, transcripts, and products

General gene information

Other Names

  • ferritin, heavy polypeptide 1 pseudogene 16
  • ferritin, heavy polypeptide-like 16

NCBI Reference Sequences (RefSeq)

NEW Try the new Transcript table

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_007337.2 

    Range
    101..1018
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000011.10 Reference GRCh38.p13 Primary Assembly

    Range
    77734315..77735232 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001008698.1: Suppressed sequence

    Description
    NM_001008698.1: This RefSeq record was removed by NCBI staff. Contact info@ncbi.nlm.nih.gov for further information.
Support Center