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TRGV5P T cell receptor gamma variable 5P (pseudogene) [ Homo sapiens (human) ]

Gene ID: 6979, updated on 10-Oct-2023

Summary

Official Symbol
TRGV5Pprovided by HGNC
Official Full Name
T cell receptor gamma variable 5P (pseudogene)provided by HGNC
Primary source
HGNC:HGNC:12291
See related
Ensembl:ENSG00000228668 IMGT/GENE-DB:TRGV5P; AllianceGenome:HGNC:12291
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
V1S5P; TCRGV5P
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Genomic context

Location:
7p14.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (38345030..38345499, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (38501913..38502382, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (38384631..38385100, complement)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene T cell receptor gamma locus Neighboring gene T cell receptor gamma variable 7 (pseudogene) Neighboring gene ATAC-STARR-seq lymphoblastoid active region 25867 Neighboring gene T cell receptor gamma locus antisense RNA 1 Neighboring gene T cell receptor gamma variable 6 (pseudogene) Neighboring gene T cell receptor gamma variable 5 Neighboring gene T cell receptor gamma variable 4

Genomic regions, transcripts, and products

General gene information

Other Names

  • T cell receptor gamma variable 5 pseudogene
  • T-cell receptor TRG locus TRGV5P*02
  • T-cell receptor TRG locus TRGV5P*02_S1431
  • T-cell receptor, gamma, variable region V5P (pseudogene)

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_001336.2 

    Range
    28449..28918
    Download
    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_000007.14 Reference GRCh38.p14 Primary Assembly

    Range
    38345030..38345499 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060931.1 Alternate T2T-CHM13v2.0

    Range
    38501913..38502382 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)