TIGAR
Fructose-2,6-bisphosphatase TIGAR
Also known as: C12orf5, TIGAR_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NQ88
- Gene
- TIGAR
- Ensembl
- ENSG00000078237
- Chromosome
- 12
- Canonical length
- 270 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
This gene is regulated as part of the p53 tumor suppressor pathway and encodes a protein with sequence similarity to the bisphosphate domain of the glycolytic enzyme that degrades fructose-2,6-bisphosphate. The protein functions by blocking glycolysis and directing the pathway into the pentose phosphate shunt. Expression of this protein also protects cells from DNA damaging reactive oxygen species and provides some protection from DNA damage-induced apoptosis. The 12p13.32 region that includes this gene is paralogous to the 11q13.3 region. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
270 residues, UniProt reviewed canonical sequence.
>Q9NQ88|TIGAR
1 MARFALTVVR HGETRFNKEK IIQGQGVDEP LSETGFKQAA AAGIFLNNVK FTHAFSSDLM
61 RTKQTMHGIL ERSKFCKDMT VKYDSRLRER KYGVVEGKAL SELRAMAKAA REECPVFTPP
121 GGETLDQVKM RGIDFFEFLC QLILKEADQK EQFSQGSPSN CLETSLAEIF PLGKNHSSKV
181 NSDSGIPGLA ASVLVVSHGA YMRSLFDYFL TDLKCSLPAT LSRSELMSVT PNTGMSLFII
241 NFEEGREVKP TVQCICMNLQ DHLNGLTETRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TIGAR can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.27
- Highest tissue expression
- 2.9 nTPM
Expression across tissuesHPA
Tissue
- spinal cord: 2.9 nTPM
- skeletal muscle: 2.7 nTPM
- midbrain: 2.5 nTPM
- pituitary gland: 2.4 nTPM
- cerebral cortex: 2.2 nTPM
- hippocampal formation: 2.1 nTPM
Single-cell type
- renal collecting duct principal cells: 31 nCPM
- renal collecting duct intercalated cells: 25 nCPM
- papillary tip epithelial cells: 25 nCPM
- renal connecting tubule cells: 22 nCPM
- loop of henle epithelial cells: 18 nCPM
- proximal tubule cells: 16 nCPM
Immune cell
- intermediate monocyte: 3.3 nTPM
- non-classical monocyte: 3.3 nTPM
- myeloid DC: 1.9 nTPM
- classical monocyte: 1.7 nTPM
- plasmacytoid DC: 1.6 nTPM
- T-reg: 1.4 nTPM
Brain region
- cerebral cortex: 9.1 nTPM
- white matter: 7.6 nTPM
- hippocampal formation: 7.5 nTPM
- spinal cord: 7.4 nTPM
- midbrain: 7.3 nTPM
- pons: 7.3 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.55
- gnomAD pLI
- 0.73
- DepMap mean gene effect
- 0.06
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cardiac muscle cell apoptotic process
- cellular response to cobalt ion
- cellular response to hypoxia
- DNA damage response
- fructose 2,6-bisphosphate metabolic process
- glucose catabolic process to lactate via pyruvate
- glycolytic process
- intestinal epithelial cell development
- mitophagy
- negative regulation of glucose catabolic process to lactate via pyruvate
- negative regulation of glycolytic process
- negative regulation of mitophagy
- negative regulation of programmed cell death
- negative regulation of reactive oxygen species metabolic process
- positive regulation of cardiac muscle cell apoptotic process
- positive regulation of DNA repair
- positive regulation of pentose-phosphate shunt
- reactive oxygen species metabolic process
- response to gamma radiation
- response to ischemia
- response to xenobiotic stimulus
- positive regulation of hexokinase activity
- regulation of pentose-phosphate shunt
- regulation of response to DNA damage checkpoint signaling
Molecular functions
- 6-bisphosphate 2-phosphatase activity
- fructose-2
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of TIGAR in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TIGAR as an antibody target. Whether an autoantibody or antibody against TIGAR could matter depends on whether native TIGAR is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TIGAR is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label TIGAR as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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