Ighv8-5 immunoglobulin heavy variable V8-5 [Mus musculus (house mouse)] - Gene

Summary

Official Symbol: Ighv8-5provided by MGI
Official Full Name: immunoglobulin heavy variable V8-5provided by MGI
Primary source: MGI:MGI:3645478
See related: IMGT/GENE-DB:IGHV8-5; AllianceGenome:MGI:3645478
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: Gm7297; EG640506
Summary: Predicted to enable antigen binding activity. Predicted to be involved in immunoglobulin mediated immune response. Orthologous to several human genes including IGHV2-5 (immunoglobulin heavy variable 2-5); IGHV2-70 (immunoglobulin heavy variable 2-70); and IGHV2-70D (immunoglobulin heavy variable 2-70D). [provided by Alliance of Genome Resources, Nov 2024]
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Genomic context

Location:: 12 F2; 12 62.49 cM

Annotation release	Status	Assembly	Chr	Location
RS_2024_02	current	GRCm39 (GCF_000001635.27)	12	NC_000078.7 (115031180..115031480, complement)
108.20200622	previous assembly	GRCm38.p6 (GCF_000001635.26)	12	NC_000078.6 (115067560..115067860, complement)

Chromosome 12 - NC_000078.7 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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Gene Ontology Provided by MGI

Function	Evidence Code	Pubs
enables antigen binding	IBA Inferred from Biological aspect of Ancestor more info

Process	Evidence Code	Pubs
involved_in immunoglobulin mediated immune response	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.