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NUTF2P5 nuclear transport factor 2 pseudogene 5 [ Homo sapiens (human) ]

Gene ID: 106481706, updated on 13-May-2022

Summary

Official Symbol
NUTF2P5provided by HGNC
Official Full Name
nuclear transport factor 2 pseudogene 5provided by HGNC
Primary source
HGNC:HGNC:50454
See related
Ensembl:ENSG00000215227 AllianceGenome:HGNC:50454
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 NUTF2P5 in Genome Data Viewer
Location:
10p13
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (13870797..13871175)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (13883877..13884257)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (13912797..13913175)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene FERM domain containing 4A Neighboring gene uncharacterized LOC105376426 Neighboring gene Sharpr-MPRA regulatory region 15561 Neighboring gene RNA, 5S ribosomal pseudogene 301 Neighboring gene Sharpr-MPRA regulatory region 6510 Neighboring gene uncharacterized LOC105376425

Genomic regions, transcripts, and products

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_043265.1 

    Range
    101..479
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000010.11 Reference GRCh38.p14 Primary Assembly

    Range
    13870797..13871175
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    13883877..13884257
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)