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FTLP8 ferritin light chain pseudogene 8 [ Homo sapiens (human) ]

Gene ID: 100462790, updated on 12-Oct-2019

Summary

Official Symbol
FTLP8provided by HGNC
Official Full Name
ferritin light chain pseudogene 8provided by HGNC
Primary source
HGNC:HGNC:37956
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

See FTLP8 in Genome Data Viewer
Location:
13q32.2
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 13 NC_000013.11 (97986949..97987225, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (98639203..98639479, complement)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105370324 Neighboring gene uncharacterized LOC105370325 Neighboring gene ribosomal protein L7a pseudogene 61 Neighboring gene importin 5 Neighboring gene uncharacterized LOC105370328 Neighboring gene uncharacterized LOC107984566 Neighboring gene FERM, ARH/RhoGEF and pleckstrin domain protein 1 Neighboring gene ring finger protein 113B

Genomic regions, transcripts, and products

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_021963.1 

    Range
    101..377
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109.20190905

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000013.11 Reference GRCh38.p13 Primary Assembly

    Range
    97986949..97987225 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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