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ELOCP17 elongin C pseudogene 17 [ Homo sapiens (human) ]

Gene ID: 100462879, updated on 23-Nov-2021

Summary

Official Symbol
ELOCP17provided by HGNC
Official Full Name
elongin C pseudogene 17provided by HGNC
Primary source
HGNC:HGNC:38153
See related
Ensembl:ENSG00000232695
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
TCEB1P17
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Genomic context

See ELOCP17 in Genome Data Viewer
Location:
Yq11.23
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) Y NC_000024.10 (25860943..25861268)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) Y NC_000024.9 (28007090..28007415)

Chromosome Y - NC_000024.10Genomic Context describing neighboring genes Neighboring gene chromodomain Y-linked 21 pseudogene Neighboring gene chromodomain Y-linked 22 pseudogene Neighboring gene OFD1 pseudogene 14 Y-linked Neighboring gene OFD1 pseudogene 18 Y-linked

Genomic regions, transcripts, and products

General gene information

Other Names

  • transcription elongation factor B (SIII), polypeptide 1 pseudogene 17
  • transcription elongation factor B subunit 1 pseudogene 17

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_004755.2 

    Range
    4050057..4050382
    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
    25860943..25861268
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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