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EIF3JP2 EIF3J pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 730021, updated on 28-Oct-2024

Summary

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Official Symbol
EIF3JP2provided by HGNC
Official Full Name
EIF3J pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:56558
See related
AllianceGenome:HGNC:56558
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

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See EIF3JP2 in Genome Data Viewer
Location:
3q25.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (150050677..150052601)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (152802056..152803979)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (149768464..149770388)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene heterogeneous nuclear ribonucleoprotein A1 pseudogene 24 Neighboring gene uncharacterized LOC124909445 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr3:149740146-149741345 Neighboring gene Sharpr-MPRA regulatory region 9408 Neighboring gene uncharacterized LOC105374153 Neighboring gene long intergenic non-protein coding RNA 1998 Neighboring gene uncharacterized LOC105374313 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr3:149824644-149825232 Neighboring gene ribosomal protein L32 pseudogene 9

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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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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Other Names

  • eukaryotic translation initiation factor 3 subunit J pseudogene

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_022279.3 

    Range
    101..2025
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    150050677..150052601
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    152802056..152803979
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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