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ELOCP4 elongin C pseudogene 4 [ Homo sapiens (human) ]

Gene ID: 100462873, updated on 8-Nov-2023

Summary

Official Symbol
ELOCP4provided by HGNC
Official Full Name
elongin C pseudogene 4provided by HGNC
Primary source
HGNC:HGNC:38141
See related
Ensembl:ENSG00000232924 AllianceGenome:HGNC:38141
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
TCEB1P4
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Genomic context

See ELOCP4 in Genome Data Viewer
Location:
Yp11.2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) Y NC_000024.10 (9230926..9231247)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) Y NC_060948.1 (8837080..8837401)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (9068535..9068856)

Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene USP9Y pseudogene 22 Neighboring gene USP9Y pseudogene 4 Neighboring gene uncharacterized LOC105379264 Neighboring gene uncharacterized LOC105379265

Genomic regions, transcripts, and products

General gene information

Other Names

  • transcription elongation factor B (SIII), polypeptide 1 pseudogene 4
  • transcription elongation factor B subunit 1 pseudogene 4

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_021935.1 

    Range
    101..422
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    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_000024.10 Reference GRCh38.p14 Primary Assembly

    Range
    9230926..9231247
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 PATCHES

Genomic

  1. NW_025791821.1 Reference GRCh38.p14 PATCHES

    Range
    98208..98529
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060948.1 Alternate T2T-CHM13v2.0

    Range
    8837080..8837401
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)