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EIF4A1P6 eukaryotic translation initiation factor 4A1 pseudogene 6 [ Homo sapiens (human) ]

Gene ID: 390407, updated on 10-Dec-2024

Summary

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Official Symbol
EIF4A1P6provided by HGNC
Official Full Name
eukaryotic translation initiation factor 4A1 pseudogene 6provided by HGNC
Primary source
HGNC:HGNC:37925
See related
Ensembl:ENSG00000236608 AllianceGenome:HGNC:37925
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 EIF4A1P6 in Genome Data Viewer
Location:
13q21.2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (60636719..60638111, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (59856376..59857768, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (61210853..61212245, complement)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105370230 Neighboring gene RNA, 5S ribosomal pseudogene 31 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr13:61203144-61203823 Neighboring gene ReSE screen-validated silencer GRCh37_chr13:61211939-61212099 Neighboring gene long intergenic non-protein coding RNA 378 Neighboring gene meiotic recombination hotspot P Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr13:61270524-61271060 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr13:61283822-61284322 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr13:61284323-61284823 Neighboring gene Sharpr-MPRA regulatory region 6777 Neighboring gene RNY3 pseudogene 5

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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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_022897.2 

    Range
    101..1493
    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_000013.11 Reference GRCh38.p14 Primary Assembly

    Range
    60636719..60638111 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    59856376..59857768 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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