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EEF1A1P9 eukaryotic translation elongation factor 1 alpha 1 pseudogene 9 [ Homo sapiens (human) ]

Gene ID: 441032, updated on 13-May-2022

Summary

Official Symbol
EEF1A1P9provided by HGNC
Official Full Name
eukaryotic translation elongation factor 1 alpha 1 pseudogene 9provided by HGNC
Primary source
HGNC:HGNC:3204
See related
AllianceGenome:HGNC:3204
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
EEF1AL7
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Genomic context

See EEF1A1P9 in Genome Data Viewer
Location:
4q24
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (105484626..105486376)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (108795490..108797240)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (106405783..106407533)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene TET2 antisense RNA 1 Neighboring gene RNA, 7SL, cytoplasmic 89, pseudogene Neighboring gene inorganic pyrophosphatase 2 Neighboring gene RNA, U6 small nuclear 553, pseudogene Neighboring gene ATP synthase F1 subunit epsilon pseudogene 1 Neighboring gene PIMREG pseudogene 2

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_029161.1 

    Range
    101..1851
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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_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    105484626..105486376
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    108795490..108797240
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NR_003586.1: Suppressed sequence

    Description
    NR_003586.1: This RefSeq was permanently suppressed because it is now thought that this pseudogene is not transcribed.