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BTN3A1
Available structures
PDB	Human UniProt search: PDBe RCSB
List of PDB id codes
	4F80, 4F9L, 4F9P, 4JKW, 4K55, 4N7I, 4N7U, 4V1P
Identifiers
Aliases	BTN3A1, BT3.1, BTF5, BTN3.1, CD277, Butyrophilin, subfamily 3, member A1, butyrophilin subfamily 3 member A1
External IDs	OMIM: 613593; HomoloGene: 56016; GeneCards: BTN3A1; OMA:BTN3A1 - orthologs
Gene location (Human)
Chr.	Chromosome 6 (human)
End	26,415,208 bp
RNA expression pattern
	Top expressed in
	granulocyte; ; spleen; ; pancreatic ductal cell; ; lymph node; ; monocyte; ; blood; ; rectum; ; gallbladder; ; appendix; ; epithelium of colon;
	n/a
	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;
Biological process	activated T cell proliferation; T cell receptor signaling pathway; adaptive immune response; immune system process; regulation of immune response;
	Sources:Amigo / QuickGO
Orthologs
	11119
	n/a
	ENSG00000026950
	n/a
	O00481
	n/a
	NM_001145008; NM_001145009; NM_007048; NM_194441
	n/a
	NP_001138480; NP_001138481; NP_008979; NP_919423
	n/a
	Wikidata
View/Edit Human

Butyrophilin subfamily 3 member A1 is a protein that in humans is encoded by the BTN3A1 gene.^[3]^[4]

References

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000026950 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ Ruddy DA, Kronmal GS, Lee VK, Mintier GA, Quintana L, Domingo R Jr, Meyer NC, Irrinki A, McClelland EE, Fullan A, Mapa FA, Moore T, Thomas W, Loeb DB, Harmon C, Tsuchihashi Z, Wolff RK, Schatzman RC, Feder JN (Aug 1997). "A 1.1-Mb transcript map of the hereditary hemochromatosis locus". Genome Res. 7 (5): 441–56. doi:10.1101/gr.7.5.441. PMID 9149941.
^ "Entrez Gene: BTN3A1 butyrophilin, subfamily 3, member A1".

External links

Human BTN3A1 genome location and BTN3A1 gene details page in the UCSC Genome Browser.

Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
Mungall AJ, Palmer SA, Sims SK, et al. (2003). "The DNA sequence and analysis of human chromosome 6". Nature. 425 (6960): 805–11. Bibcode:2003Natur.425..805M. doi:10.1038/nature02055. PMID 14574404.
Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
Rhodes DA, Stammers M, Malcherek G, et al. (2001). "The cluster of BTN genes in the extended major histocompatibility complex". Genomics. 71 (3): 351–62. doi:10.1006/geno.2000.6406. PMID 11170752.
Tazi-Ahnini R, Henry J, Offer C, et al. (1998). "Cloning, localization, and structure of new members of the butyrophilin gene family in the juxta-telomeric region of the major histocompatibility complex". Immunogenetics. 47 (1): 55–63. doi:10.1007/s002510050326. PMID 9382921. S2CID 1873778.
Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.

This article on a gene on human chromosome 6 is a stub. You can help Wikipedia by expanding it.

[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000026950 – Ensembl, May 2017

[2] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[pmid9149941-3] Ruddy DA, Kronmal GS, Lee VK, Mintier GA, Quintana L, Domingo R Jr, Meyer NC, Irrinki A, McClelland EE, Fullan A, Mapa FA, Moore T, Thomas W, Loeb DB, Harmon C, Tsuchihashi Z, Wolff RK, Schatzman RC, Feder JN (Aug 1997). "A 1.1-Mb transcript map of the hereditary hemochromatosis locus". Genome Res. 7 (5): 441–56. doi:10.1101/gr.7.5.441. PMID 9149941.

[entrez-4] "Entrez Gene: BTN3A1 butyrophilin, subfamily 3, member A1".

[1]

[2]

[3]

[4]

Butyrophilin, subfamily 3, member A1

References

External links

Further reading