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FTLP17 ferritin light chain pseudogene 17 [ Homo sapiens (human) ]

Gene ID: 642337, updated on 10-Oct-2023

Summary

Official Symbol
FTLP17provided by HGNC
Official Full Name
ferritin light chain pseudogene 17provided by HGNC
Primary source
HGNC:HGNC:37967
See related
AllianceGenome:HGNC:37967
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

Location:
1p21.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (104153329..104154037, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (104195755..104196463, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (104695951..104696659, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105378879 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr1:104677494-104678215 Neighboring gene THAP3 pseudogene 1 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr1:104949659-104950858 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr1:105248976-105250175 Neighboring gene uncharacterized LOC105378880 Neighboring gene MPRA-validated peak344 silencer Neighboring gene MPRA-validated peak345 silencer Neighboring gene NANOG hESC enhancer GRCh37_chr1:105879928-105880429 Neighboring gene MPRA-validated peak346 silencer Neighboring gene cyclin dependent kinase 4 pseudogene 1

Genomic regions, transcripts, and products

Phenotypes

EBI GWAS Catalog

Description
Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
EBI GWAS Catalog

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_023171.2 

    Range
    101..809
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    104153329..104154037 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    104195755..104196463 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)