IFNA16

IFNA16
Identifiers
Aliases	IFNA16, IFN-alphaO, IFN-alpha-16, interferon, alpha 16, interferon alpha 16
External IDs	OMIM: 147580; MGI: 2667155; HomoloGene: 105364; GeneCards: IFNA16; OMA:IFNA16 - orthologs
Gene location (Human)
Chr.	Chromosome 9 (human)
End	21,217,311 bp
Gene location (Mouse)
Chr.	Chromosome 4 (mouse)
End	88,562,696 bp
RNA expression pattern
	Top expressed in
	cell; ; monocyte;
	Top expressed in
	embryo; ; embryo;
	More reference expression data
	n/a
Gene ontology
Molecular function	cytokine activity; type I interferon receptor binding; cytokine receptor binding;
Cellular component	extracellular region; extracellular space;
Biological process	natural killer cell activation involved in immune response; B cell differentiation; defense response; B cell proliferation; blood coagulation; positive regulation of peptidyl-serine phosphorylation of STAT protein; humoral immune response; adaptive immune response; defense response to virus; type I interferon signaling pathway; response to exogenous dsRNA; T cell activation involved in immune response; cytokine-mediated signaling pathway; innate immune response; regulation of signaling receptor activity;
	Sources:Amigo / QuickGO
Orthologs
	3449
	230396
	ENSG00000147885
	ENSMUSG00000063376
	P05015
	Q80SU4
	NM_002173
	NM_177347
	NP_002164
	NP_796321
	Wikidata
View/Edit Human	View/Edit Mouse

Interferon alpha-16, also known as IFN-alpha-16, is a protein that in humans is encoded by theIFNA16 gene.^[5]^[6]

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000147885 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000063376 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Entrez Gene: interferon".
^ Olopade OI, Bohlander SK, Pomykala H, Maltepe E, Van Melle E, Le Beau MM, Diaz MO (October 1992). "Mapping of the shortest region of overlap of deletions of the short arm of chromosome 9 associated with human neoplasia". Genomics. 14 (2): 437–43. doi:10.1016/S0888-7543(05)80238-1. PMID 1385305.