Trav7d-4 T cell receptor alpha variable 7D-4 [Mus musculus (house mouse)] - Gene

Summary

Official Symbol: Trav7d-4provided by MGI
Official Full Name: T cell receptor alpha variable 7D-4provided by MGI
Primary source: MGI:MGI:3651273
See related: Ensembl:ENSMUSG00000094023 IMGT/GENE-DB:TRAV7D-4; AllianceGenome:MGI:3651273
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: Gm13959
Summary: Predicted to enable peptide antigen binding activity. Orthologous to human TRAV12-1 (T cell receptor alpha variable 12-1); TRAV12-2 (T cell receptor alpha variable 12-2); and TRAV12-3 (T cell receptor alpha variable 12-3). [provided by Alliance of Genome Resources, Dec 2024]
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Genomic context

Location:: 14 C2; 14 27.08 cM

Annotation release	Status	Assembly	Chr	Location
RS_2024_02	current	GRCm39 (GCF_000001635.27)	14	NC_000080.7 (53007320..53007849)
108.20200622	previous assembly	GRCm38.p6 (GCF_000001635.26)	14	NC_000080.6 (52769863..52770392)

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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Other Names

T-cell receptor alpha variable region 7D-4

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.