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FTH1P27 ferritin heavy chain 1 pseudogene 27 [ Homo sapiens (human) ]

Gene ID: 100270709, updated on 11-Jun-2021

Summary

Official Symbol
FTH1P27provided by HGNC
Official Full Name
ferritin heavy chain 1 pseudogene 27provided by HGNC
Primary source
HGNC:HGNC:39091
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

See FTH1P27 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 (37505267..37506035)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (37364520..37365288)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene proline rich and Gla domain 1 Neighboring gene ferritin heavy chain like 17 pseudogene Neighboring gene ferritin heavy chain 1 pseudogene 19 Neighboring gene family with sequence similarity 47 member D, pseudogene Neighboring gene LanC like 3

Genomic regions, transcripts, and products

General gene information

Other Names

  • ferritin, heavy polypeptide 1 pseudogene 27
  • ferritin, heavy polypeptide-like 17 pseudogene

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_009568.3 

    Range
    101..869
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    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
    37505267..37506035
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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