Butyrophilin, subfamily 2, member A2

BTN2A2
Identifiers
Aliases	BTN2A2, BT2.2, BTF2, BTN2.2, Butyrophilin, subfamily 2, member A2, butyrophilin subfamily 2 member A2
External IDs	OMIM: 613591; MGI: 3606486; HomoloGene: 56012; GeneCards: BTN2A2; OMA:BTN2A2 - orthologs
Gene location (Human)
Chr.	Chromosome 6 (human)
End	26,394,874 bp
Gene location (Mouse)
Chr.	Chromosome 13 (mouse)
End	23,673,027 bp
RNA expression pattern
	Top expressed in
	epithelium of nasopharynx; ; lymph node; ; tonsil; ; granulocyte; ; appendix; ; monocyte; ; tendon of biceps brachii; ; spleen; ; pancreatic ductal cell; ; cerebellar cortex;
	Top expressed in
	embryo; ; embryo; ; secondary oocyte; ; morula; ; primary oocyte; ; epiblast; ; blastocyst; ; primary visual cortex; ; placenta; ; hippocampus proper;
	More reference expression data
	; ;
	More reference expression data
Gene ontology
Molecular function	protein binding; signaling receptor binding;
Cellular component	integral component of membrane; membrane; plasma membrane; external side of plasma membrane; cell surface;
Biological process	negative regulation of activated T cell proliferation; negative regulation of cellular metabolic process; negative regulation of phosphatidylinositol 3-kinase signaling; positive regulation of regulatory T cell differentiation; regulation of immune response; T cell receptor signaling pathway; negative regulation of T cell receptor signaling pathway; negative regulation of protein kinase B signaling; negative regulation of ERK1 and ERK2 cascade; negative regulation of G1/S transition of mitotic cell cycle;
	Sources:Amigo / QuickGO
Orthologs
	10385
	238555
	ENSG00000124508
	ENSMUSG00000053216
	Q8WVV5
	A4QPC6
NM_001197237; NM_001197238; NM_001197239; NM_001197240; NM_006995;
	NM_181531
	NM_001289614; NM_001289615; NM_175938
NP_001184166; NP_001184167; NP_001184168; NP_001184169; NP_008926;
	NP_853509; NP_001184166.1; NP_008926.2
	NP_001276543; NP_001276544; NP_787952
	Wikidata
View/Edit Human	View/Edit Mouse

Butyrophilin subfamily 2 member A2 is a protein that in humans is encoded by the BTN2A2 gene.