JAM2 junctional adhesion molecule 2 [Bos taurus (cattle)] - Gene

Summary

Official Symbol: JAM2provided by VGNC
Official Full Name: junctional adhesion molecule 2provided by VGNC
Primary source: VGNC:VGNC:50011
See related: BGD:BT23127; Ensembl:ENSBTAG00000000603
Gene type: protein coding
RefSeq status: PROVISIONAL
Organism: Bos taurus
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Laurasiatheria; Artiodactyla; Ruminantia; Pecora; Bovidae; Bovinae; Bos
Orthologs: human mouse all
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Genomic context

Location:: chromosome: 1

Exon count:: 10

Annotation release	Status	Assembly	Chr	Location
RS_2023_09	current	ARS-UCD2.0 (GCF_002263795.3)	1	NC_037328.1 (10704997..10787558, complement)

Chromosome 1 - NC_037328.1 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Go to reference sequence details

Genomic Sequence:: NC_037328.1 Chromosome 1 Reference ARS-UCD2.0 Primary Assembly

Go to nucleotide: Graphics FASTA GenBank

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

JAM2 (e-PCR)
- UniSTS:506178

BZ902891 (e-PCR)
- UniSTS:474781

Gene Ontology Provided by RefSeq

Process	Evidence Code	Pubs
involved_in leukocyte tethering or rolling	IEA Inferred from Electronic Annotation more info	PubMed

Component	Evidence Code	Pubs
located_in cell surface	IEA Inferred from Electronic Annotation more info	PubMed
part_of protein complex involved in cell adhesion	IEA Inferred from Electronic Annotation more info	PubMed
located_in tight junction	IEA Inferred from Electronic Annotation more info	PubMed

General protein information

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Preferred Names: junctional adhesion molecule B

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.