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FTH1P4 ferritin heavy chain 1 pseudogene 4 [ Homo sapiens (human) ]

Gene ID: 2499, updated on 11-Sep-2019

Summary

Official Symbol
FTH1P4provided by HGNC
Official Full Name
ferritin heavy chain 1 pseudogene 4provided by HGNC
Primary source
HGNC:HGNC:3991
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
FTHL4

Genomic context

See FTH1P4 in Genome Data Viewer
Location:
3q21.3
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 3 NC_000003.12 (128764306..128765217, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (128483149..128484064, complement)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene POU class 5 homeobox 1 pseudogene 6 Neighboring gene RAB7A, member RAS oncogene family Neighboring gene microtubule affinity regulating kinase 2 pseudogene 8 Neighboring gene RNA, 7SL, cytoplasmic 698, pseudogene Neighboring gene ribosomal protein S15a pseudogene 16

Genomic regions, transcripts, and products

General gene information

Other Names

  • ferritin, heavy polypeptide 1 pseudogene 4
  • ferritin, heavy polypeptide-like 4 pseudogene

NCBI Reference Sequences (RefSeq)

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_004769.6 

    Range
    101..1012
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109 details...Open this link in a new tab

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000003.12 Reference GRCh38.p13 Primary Assembly

    Range
    128764306..128765217 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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