Human Gene IFNG (ENST00000229135.4) Description and Page Index
  Description: Homo sapiens interferon gamma (IFNG), mRNA. (from RefSeq NM_000619)
Gencode Transcript: ENST00000229135.4
Gencode Gene: ENSG00000111537.5
Transcript (Including UTRs)
   Position: hg38 chr12:68,154,768-68,159,740 Size: 4,973 Total Exon Count: 4 Strand: -
Coding Region
   Position: hg38 chr12:68,155,353-68,159,615 Size: 4,263 Coding Exon Count: 4 

Page IndexSequence and LinksUniProtKB CommentsProtein StructureOther NamesMethods
Data last updated at UCSC: 2021-06-20 19:51:40

+  Sequence and Links to Tools and Databases
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-  Comments and Description Text from UniProtKB
  ID: IFNG_HUMAN
DESCRIPTION: RecName: Full=Interferon gamma; Short=IFN-gamma; AltName: Full=Immune interferon; Flags: Precursor;
FUNCTION: Produced by lymphocytes activated by specific antigens or mitogens. IFN-gamma, in addition to having antiviral activity, has important immunoregulatory functions. It is a potent activator of macrophages, it has antiproliferative effects on transformed cells and it can potentiate the antiviral and antitumor effects of the type I interferons.
SUBUNIT: Homodimer.
SUBCELLULAR LOCATION: Secreted.
TISSUE SPECIFICITY: Released primarily from activated T lymphocytes.
PTM: Proteolytic processing produces C-terminal heterogeneity, with proteins ending alternatively at Gly-150, Met-157 or Gly-161.
DISEASE: In Caucasians, genetic variation in IFNG is associated with the risk of aplastic anemia (AA) [MIM:609135]. AA is a rare disease in which the reduction of the circulating blood cells results from damage to the stem cell pool in bone marrow. In most patients, the stem cell lesion is caused by an autoimmune attack. T-lymphocytes, activated by an endogenous or exogenous, and most often unknown antigenic stimulus, secrete cytokines, including IFN-gamma, which would in turn be able to suppress hematopoiesis.
PHARMACEUTICAL: Available under the name Actimmune (Genentech). Used for reducing the frequency and severity of serious infections associated with chronic granulomatous disease (CGD).
SIMILARITY: Belongs to the type II (or gamma) interferon family.
WEB RESOURCE: Name=GeneReviews; URL="http://www.ncbi.nlm.nih.gov/sites/GeneTests/lab/gene/IFNG";
WEB RESOURCE: Name=Wikipedia; Note=Interferon gamma entry; URL="http://en.wikipedia.org/wiki/Interferon_gamma";
WEB RESOURCE: Name=SeattleSNPs; URL="http://pga.gs.washington.edu/data/ifng/";

+  Protein Domain and Structure Information
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-  Other Names for This Gene
  UCSC ID: ENST00000229135.4
Representative RNA: NM_000619
Protein: P01579 (aka IFNG_HUMAN)

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.