Trav14-3 T cell receptor alpha variable 14-3 [Mus musculus (house mouse)] - Gene

Summary

Official Symbol: Trav14-3provided by MGI
Official Full Name: T cell receptor alpha variable 14-3provided by MGI
Primary source: MGI:MGI:3702149
See related: Ensembl:ENSMUSG00000094212 IMGT/GENE-DB:TRAV14-3; AllianceGenome:MGI:3702149
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: Gm13933
Summary: Predicted to enable peptide antigen binding activity. Orthologous to human TRAV23DV6 (T cell receptor alpha variable 23/delta variable 6). [provided by Alliance of Genome Resources, Nov 2024]
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Genomic context

Location:: 14 C2; 14 27.5 cM

Annotation release	Status	Assembly	Chr	Location
RS_2024_02	current	GRCm39 (GCF_000001635.27)	14	NC_000080.7 (54000653..54001151)
108.20200622	previous assembly	GRCm38.p6 (GCF_000001635.26)	14	NC_000080.6 (53763196..53763694)

Chromosome 14 - NC_000080.7 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

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Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

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General gene information

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Markers

D14Mit21 (e-PCR), detects polymorphism
- UniSTS:127323

Other Names

T cell receptor alpha variable region 14-3

Gene Ontology Provided by MGI

Function	Evidence Code	Pubs
enables molecular_function	ND No biological Data available more info
enables peptide antigen binding	IBA Inferred from Biological aspect of Ancestor more info

Process	Evidence Code	Pubs
involved_in biological_process	ND No biological Data available more info

Component	Evidence Code	Pubs
is_active_in cellular_component	ND No biological Data available 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.