IFNA13

IFNA13
Available structures
PDB	Human UniProt search: PDBe RCSB
List of PDB id codes
	3UX9
Identifiers
Aliases	IFNA13, interferon alpha 13
External IDs	OMIM: 147578; HomoloGene: 136811; GeneCards: IFNA13; OMA:IFNA13 - orthologs
Gene location (Human)
Chr.	Chromosome 9 (human)
End	21,368,962 bp
RNA expression pattern
	Top expressed in
	corpus callosum; ; putamen; ; primary visual cortex; ; caudate nucleus; ; Brodmann area 9; ; amygdala; ; hippocampus proper; ; gastric mucosa; ; stromal cell of endometrium; ; substantia nigra;
	n/a
	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
	3447
	n/a
	ENSG00000233816
	n/a
	P01562
	n/a
	NM_006900
	n/a
	NP_076918
	n/a
	Wikidata
View/Edit Human

Interferon alpha-1/13, also known as IFN-alpha-1/13, is a protein that in humans is encoded by the IFNA1 and IFNA13 genes.^[3]^[4]

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000233816 – Ensembl, May 2017
^ "Human 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.