Trgv1 T cell receptor gamma, variable 1 [Mus musculus (house mouse)] - Gene

Summary

Official Symbol: Trgv1provided by MGI
Official Full Name: T cell receptor gamma, variable 1provided by MGI
Primary source: MGI:MGI:98631
See related: Ensembl:ENSMUSG00000076755 IMGT/GENE-DB:TRGV1; AllianceGenome:MGI:98631
Gene type: other
RefSeq status: VALIDATED
Organism: Mus musculus
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Mus; Mus
Also known as: Gm16602; Tcrg-V1
Summary: Predicted to be active in external side of plasma membrane. Orthologous to human TRGV11 (T cell receptor gamma variable 11 (non-functional)). [provided by Alliance of Genome Resources, Dec 2024]
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Genomic context

Location:: 13 A2; 13 6.89 cM

Annotation release	Status	Assembly	Chr	Location
RS_2024_02	current	GRCm39 (GCF_000001635.27)	13	NC_000079.7 (19524186..19524624)
108.20200622	previous assembly	GRCm38.p6 (GCF_000001635.26)	13	NC_000079.6 (19340016..19340454)

Chromosome 13 - NC_000079.7 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

The ability of T-cell receptor V gamma 1+ T cells to bind and subsequently kill activated macrophages is dependent on Fas/FasL interactions.
Title: Fas-Fas ligand interactions are essential for the binding to and killing of activated macrophages by gamma delta T cells.

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General gene information

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Gene Ontology Provided by MGI

Component	Evidence Code	Pubs
is_active_in external side of plasma membrane	IBA Inferred from Biological aspect of Ancestor more info

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.