Format

Send to:

Choose Destination

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

Gene ID: 100462873, updated on 25-Jan-2022

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
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

See ELOCP4 in Genome Data Viewer
Location:
Yp11.2
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) Y NC_000024.10 (9230926..9231247)
105.20201022 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)

NEW Try the new Transcript table

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
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000024.10 Reference GRCh38.p13 Primary Assembly

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