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TRBVB T cell receptor beta variable B (pseudogene) [ Homo sapiens (human) ]

Gene ID: 28555, updated on 17-Sep-2024

Summary

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Official Symbol
TRBVBprovided by HGNC
Official Full Name
T cell receptor beta variable B (pseudogene)provided by HGNC
Primary source
HGNC:HGNC:12248
See related
Ensembl:ENSG00000241911 IMGT/GENE-DB:TRBVB; AllianceGenome:HGNC:12248
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
TCRBV34S1
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Genomic context

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See TRBVB in Genome Data Viewer
Location:
7q34
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (142711384..142711924)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (144067090..144067630)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (142419212..142419752)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene T cell receptor beta locus Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr7:142403795-142404426 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr7:142404427-142405058 Neighboring gene T cell receptor beta variable A (pseudogene) Neighboring gene T cell receptor beta variable 26 (pseudogene) Neighboring gene T cell receptor beta variable 27 Neighboring gene T cell receptor beta variable 28

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. The complete 685-kilobase DNA sequence of the human beta T cell receptor locus. Rowen L, et al. Science, 1996 Jun 21. PMID 8650574

GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See Variation Viewer (GRCh37.p13)

General gene information

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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_001333.2 

    Range
    545032..545572
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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
    142711384..142711924
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 ALT_REF_LOCI_1

Genomic

  1. NT_187562.1 Reference GRCh38.p14 ALT_REF_LOCI_1

    Range
    713965..714505
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060931.1 Alternate T2T-CHM13v2.0

    Range
    144067090..144067630
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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