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EIF5AP2 eukaryotic translation initiation factor 5A pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 1986, updated on 13-May-2022

Summary

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Official Symbol
EIF5AP2provided by HGNC
Official Full Name
eukaryotic translation initiation factor 5A pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:3303
See related
Ensembl:ENSG00000267679 AllianceGenome:HGNC:3303
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

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See EIF5AP2 in Genome Data Viewer
Location:
17q25.3
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 17 NC_000017.11 (78157359..78159135)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 17 NC_060941.1 (79051456..79053231)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (76153440..76155216)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene CEB72 minisatellite repeat instability region Neighboring gene transmembrane channel like 6 Neighboring gene transmembrane channel like 8 Neighboring gene chromosome 17 open reading frame 99 Neighboring gene synaptogyrin 2 Neighboring gene thymidine kinase 1

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. The eukaryotic cofactor for the human immunodeficiency virus type 1 (HIV-1) rev protein, eIF-5A, maps to chromosome 17p12-p13: three eIF-5A pseudogenes map to 10q23.3, 17q25, and 19q13.2. Steinkasserer A, et al. Genomics, 1995 Feb 10. PMID 7759117
  2. The genomic structure encoding human initiation factor eIF-5A. Koettnitz K, et al. Gene, 1994 Jul 8. PMID 7545941

GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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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_002746.3 

    Range
    101..1877
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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_000017.11 Reference GRCh38.p14 Primary Assembly

    Range
    78157359..78159135
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060941.1 Alternate T2T-CHM13v2.0

    Range
    79051456..79053231
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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