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EIF4BP7 eukaryotic translation initiation factor 4B pseudogene 7 [ Homo sapiens (human) ]

Gene ID: 643873, updated on 10-Oct-2023

Summary

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Official Symbol
EIF4BP7provided by HGNC
Official Full Name
eukaryotic translation initiation factor 4B pseudogene 7provided by HGNC
Primary source
HGNC:HGNC:37940
See related
AllianceGenome:HGNC:37940
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 EIF4BP7 in Genome Data Viewer
Location:
Xq23
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (111617654..111621516, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (110065893..110069756, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (110860882..110864744, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene high mobility group box 1 pseudogene 12 Neighboring gene serine rich and transmembrane domain containing 2 Neighboring gene H3K27ac hESC enhancer GRCh37_chrX:110782077-110782578 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:110786721-110787234 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chrX:110792373-110792886 Neighboring gene ribosomal protein L18a pseudogene 15 Neighboring gene RNA, 5S ribosomal pseudogene 512

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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Markers

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_022961.1 

    Range
    101..3963
    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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    111617654..111621516 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    110065893..110069756 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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