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EIF4HP2 eukaryotic translation initiation factor 4H pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 100421545, updated on 13-May-2022

Summary

Official Symbol
EIF4HP2provided by HGNC
Official Full Name
eukaryotic translation initiation factor 4H pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:49036
See related
AllianceGenome:HGNC:49036
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

See EIF4HP2 in Genome Data Viewer
Location:
22q12.2
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (30902153..30902972)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (31365728..31366547)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (31298140..31298959)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene oxysterol binding protein 2 Neighboring gene uncharacterized LOC105372994 Neighboring gene origin of replication in OSBP2 Neighboring gene uncharacterized LOC107985544 Neighboring gene MORC2 antisense RNA 1 Neighboring gene MORC family CW-type zinc finger 2 Neighboring gene taurine up-regulated 1

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_027477.2 

    Range
    101..920
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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_000022.11 Reference GRCh38.p14 Primary Assembly

    Range
    30902153..30902972
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    31365728..31366547
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)