GO ID |
Ontology |
GO Term |
Term Definition |
Proteins |
GO:0002230
|
BP
|
positive regulation of defense response to virus by host
|
Any host process that results in the promotion of antiviral immune response mechanisms, thereby limiting viral replication.
|
TRAF3IP2,
IL12RB1,
MAVS,
LILRB1,
TRIM6,
APOBEC3G,
EIF2AK4,
PYCARD
|
GO:0002236
|
BP
|
detection of misfolded protein
|
The series of events in which a misfolded protein stimulus is received and converted into a molecular signal.
|
HSPD1
|
GO:0002237
|
BP
|
response to molecule of bacterial origin
|
Any process that results in a change in state or activity of an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a stimulus by molecules of bacterial origin such as peptides derived from bacterial flagellin.
|
BCL10,
CXCL8,
CXCL2,
TNFAIP3,
IL10,
CD24
|
GO:0002244
|
BP
|
hematopoietic progenitor cell differentiation
|
The process in which precursor cell type acquires the specialized features of a hematopoietic progenitor cell, a class of cell types including myeloid progenitor cells and lymphoid progenitor cells.
|
RBM47,
EML1,
ZBTB24,
TGFB1,
INHBA,
PTPRC,
TOP2A,
BMP4,
EEF2,
FST,
CEBPD,
PSEN1,
HYAL2,
ARHGEF7,
RRS1,
ESCO2,
PAPD4,
TMEM91,
SFRP1,
C12orf29,
BVES,
SSBP3,
ANLN,
WDR7,
PRRC2C
|
GO:0002246
|
BP
|
wound healing involved in inflammatory response
|
The series of events that restore integrity to damaged tissue that contribute to an inflammatory response.
|
HMOX1
|
GO:0002248
|
BP
|
connective tissue replacement involved in inflammatory response wound healing
|
The series of events leading to growth of connective tissue when loss of tissues that are incapable of regeneration occurs, or when fibrinous exudate cannot be adequately cleared that contribute to an inflammatory response.
|
TGFB1,
IL1A,
F2R,
HIF1A
|
GO:0002250
|
BP
|
adaptive immune response
|
An immune response based on directed amplification of specific receptors for antigen produced through a somatic diversification process, and allowing for enhanced response to subsequent exposures to the same antigen (immunological memory).
|
PIK3CD,
RIPK2,
JAK2,
TNFRSF21,
BCL10,
IFNA1 ,
CD4,
FGA,
FGB,
ANXA1,
IFNA16,
PRKCB,
FYN,
CTSL,
LYN,
CTSH,
HLA-E,
CD46,
RAG1,
TFEB,
CTSS,
CD6,
GPR183,
CSK,
SYK,
PIK3CG,
JAK3,
ALCAM,
ADGRE1,
MARCH8,
LAIR1,
ERAP2,
RNF19B,
VTCN1,
IFNE,
LILRB1,
TRPM4,
CLEC4D,
FCGR1B,
OTUB1,
DCLRE1C,
JAM3,
PRKD2,
CD244,
CD209,
PAG1,
ERAP1,
EIF2AK4,
LAMP3,
TNFRSF11A
|
GO:0002260
|
BP
|
lymphocyte homeostasis
|
The process of regulating the proliferation and elimination of lymphocytes such that the total number of lymphocytes within a whole or part of an organism is stable over time in the absence of an outside stimulus.
|
SKIL,
SLC40A1
|
GO:0002262
|
BP
|
myeloid cell homeostasis
|
The process of regulating the proliferation and elimination of myeloid cells such that the total number of myeloid cells within a whole or part of an organism is stable over time in the absence of an outside stimulus.
|
BCL2L11,
BAX,
FOXP3
|
GO:0002263
|
BP
|
cell activation involved in immune response
|
A change in the morphology or behavior of a cell resulting from exposure to an activating factor such as a cellular or soluble ligand, leading to the initiation or perpetuation of an immune response.
|
GBF1
|
GO:0002268
|
BP
|
follicular dendritic cell differentiation
|
The process in which a relatively unspecialized precursor cell acquires the specialized features of a follicular dendritic cell.
|
BCL3
|
GO:0002277
|
BP
|
myeloid dendritic cell activation involved in immune response
|
The change in morphology and behavior of a myeloid dendritic cell resulting from exposure to a cytokine, chemokine, cellular ligand, or soluble factor, leading to the initiation or perpetuation of an immune response.
|
DOCK2,
PYCARD
|
GO:0002281
|
BP
|
macrophage activation involved in immune response
|
A change in morphology and behavior of a macrophage resulting from exposure to a cytokine, chemokine, cellular ligand, or soluble factor, leading to the initiation or perpetuation of an immune response.
|
TYROBP,
SYK
|
GO:0002282
|
BP
|
microglial cell activation involved in immune response
|
The change in morphology and behavior of a microglial cell resulting from exposure to a cytokine, chemokine, cellular ligand, or soluble factor, leading to the initiation or perpetuation of an immune response.
|
TLR3,
IL33
|
GO:0002283
|
BP
|
neutrophil activation involved in immune response
|
The change in morphology and behavior of a neutrophil resulting from exposure to a cytokine, chemokine, cellular ligand, or soluble factor, leading to the initiation or perpetuation of an immune response.
|
TYROBP,
SYK
|
GO:0002286
|
BP
|
T cell activation involved in immune response
|
The change in morphology and behavior of a mature or immature T cell resulting from exposure to a mitogen, cytokine, chemokine, cellular ligand, or an antigen for which it is specific, leading to the initiation or perpetuation of an immune response.
|
IFNA1 ,
IFNA16,
LCP1,
PSEN1,
F2RL1,
IFNE,
EIF2AK4
|
GO:0002291
|
BP
|
T cell activation via T cell receptor contact with antigen bound to MHC molecule on antigen presenting cell
|
The change in morphology and behavior of a mature or immature T cell resulting from exposure to an antigen for which its T cell receptor is specific bound to an MHC molecule on an antigen presenting cell, leading to the initiation or perpetuation of an immune response.
|
ICAM1
|
GO:0002292
|
BP
|
T cell differentiation involved in immune response
|
The process in which an antigenically naive T cell acquires the specialized features of an effector, regulatory, or memory T cell as part of an immune response. Effector T cells include cells which provide T cell help or exhibit cytotoxicity towards other cells.
|
CLEC4D
|
GO:0002309
|
BP
|
T cell proliferation involved in immune response
|
The expansion of a T cell population by cell division as part of an immune response.
|
SLC11A1,
RPS6,
LILRB1
|
GO:0002312
|
BP
|
B cell activation involved in immune response
|
The change in morphology and behavior of a mature or immature B cell during an immune response, resulting from exposure to a mitogen, cytokine, chemokine, cellular ligand, or an antigen for which it is specific.
|
GPR183
|
GO:0002313
|
BP
|
mature B cell differentiation involved in immune response
|
The process in which a naive B cell acquires the specialized features of a mature or memory B cell during an immune response.
|
GPR183
|
GO:0002314
|
BP
|
germinal center B cell differentiation
|
The process in which a B cell in the spleen acquires the specialized features of a germinal center B cell. Germinal center B cells are rapidly cycling B cells which have downregulated IgD expression and exhibit high levels of binding by peanut agglutinin (PNA).
|
ADA,
CDH17,
ITFG2
|
GO:0002315
|
BP
|
marginal zone B cell differentiation
|
The process in which a B cell in the spleen acquires the specialized features of a marginal zone B cell. Marginal zone B cells are localized in a distinct anatomical region of the spleen that represents the major antigen-filtering and scavenging area (by specialized macrophages resident there). It appears that they are preselected to express a BCR repertoire similar to B-1 B cells, biased toward bacterial cell wall constituents and senescent self-components (such as oxidized LDL).
|
BCL3,
NOTCH2,
CDH17
|
GO:0002316
|
BP
|
follicular B cell differentiation
|
The process in which a B cell in the spleen acquires the specialized features of a follicular B cell. Follicular B cells are major population of mature recirculating B cells in the spleen and are located in the B-cell follicle region.
|
PLCG2
|
GO:0002317
|
BP
|
plasma cell differentiation
|
The process in which a B cell acquires the specialized features of a plasma cell. A plasma cell is a lymphocyte which develops from a B cell and produces high amounts of antibody.
|
ITM2A,
LGALS1
|
GO:0002318
|
BP
|
myeloid progenitor cell differentiation
|
The process in which a precursor cell type acquires the specialized features of a myeloid progenitor cell. Myeloid progenitor cells include progenitor cells for any of the myeloid lineages.
|
KIT,
JAM3
|
GO:0002320
|
BP
|
lymphoid progenitor cell differentiation
|
The process in which a precursor cell type acquires the specialized features of a lymphoid progenitor cell. Lymphoid progenitor cells include progenitor cells for any of the lymphoid lineages.
|
BCL2,
KIT,
BMP4
|
GO:0002322
|
BP
|
B cell proliferation involved in immune response
|
The expansion of a B cell population by cell division following B cell activation during an immune response.
|
TLR4,
PLCL2
|
GO:0002323
|
BP
|
natural killer cell activation involved in immune response
|
The change in morphology and behavior of a natural killer cell resulting from exposure a cytokine, chemokine, cellular ligand, or soluble factor, leading to the initiation or perpetuation of an immune response.
|
IFNA1 ,
IFNA16,
IFNE,
CD244
|
GO:0002326
|
BP
|
B cell lineage commitment
|
The process in which a lymphoid progenitor cell becomes committed to become any type of B cell.
|
BCL2,
TCF3,
PRKDC
|
GO:0002327
|
BP
|
immature B cell differentiation
|
The process in which a precursor cell type acquires the specialized features of an immature B cell.
|
KIT,
FNIP1
|
GO:0002328
|
BP
|
pro-B cell differentiation
|
The process in which a precursor cell type acquires the specialized features of a pro-B cell. Pro-B cells are the earliest stage of the B cell lineage and undergo heavy chain D and J gene rearrangements, although they are not fully committed.
|
PRKDC,
SOX4
|
GO:0002329
|
BP
|
pre-B cell differentiation
|
The process in which a precursor cell type acquires the specialized features of a pre-B cell. Pre-B cells follow the pro-B cell stage of immature B cell differentiation and undergo rearrangement of heavy chain V, D, and J gene segments.
|
LRRC8A
|
GO:0002331
|
BP
|
pre-B cell allelic exclusion
|
Expression of a single heavy chain allele during pre-B cell differentiation.
|
RAG1
|
GO:0002337
|
BP
|
B-1a B cell differentiation
|
The process in which B cells acquire the specialized features of B-1a B cells. B-1a B cells are B-1 cells that express CD5 and arise from fetal liver precursors.
|
PLCL2
|
GO:0002347
|
BP
|
response to tumor cell
|
Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a stimulus from a tumor cell.
|
HNMT
|
GO:0002352
|
BP
|
B cell negative selection
|
Any process leading to negative selection in B cells. Mechanisms of negative selection include anergy and deletion.
|
BAX
|
GO:0002358
|
BP
|
B cell homeostatic proliferation
|
The non-specific expansion of B cell populations within a whole or part of an organism to reach to a total number of B cells which will then remain stable over time in the absence of an external stimulus.
|
BAX
|
GO:0002360
|
BP
|
T cell lineage commitment
|
The process in which a lymphoid progenitor cell becomes committed to becoming any type of T cell.
|
PRKDC
|
GO:0002362
|
BP
|
CD4-positive, CD25-positive, alpha-beta regulatory T cell lineage commitment
|
The process in which a CD4-positive, alpha-beta T cell becomes committed to becoming a CD4-positive, CD25-positive, alpha-beta regulatory T cell.
|
FOXP3
|
GO:0002366
|
BP
|
leukocyte activation involved in immune response
|
A change in morphology and behavior of a leukocyte resulting from exposure to a specific antigen, mitogen, cytokine, cellular ligand, or soluble factor, leading to the initiation or perpetuation of an immune response.
|
SYK,
CLEC7A
|
GO:0002367
|
BP
|
cytokine production involved in immune response
|
The appearance of a cytokine due to biosynthesis or secretion following a cellular stimulus contributing to an immune response, resulting in an increase in its intracellular or extracellular levels.
|
MR1
|
GO:0002368
|
BP
|
B cell cytokine production
|
Any process that contributes to cytokine production by a B cell.
|
HSPD1
|
GO:0002369
|
BP
|
T cell cytokine production
|
Any process that contributes to cytokine production by a T cell.
|
SLC11A1,
DLG1
|
GO:0002371
|
BP
|
dendritic cell cytokine production
|
Any process that contributes to cytokine production by a dendritic cell.
|
KIT
|
GO:0002374
|
BP
|
cytokine secretion involved in immune response
|
The regulated release of cytokines from a cell that contributes to an immune response.
|
TLR2,
TREM1
|
GO:0002376
|
BP
|
immune system process
|
Any process involved in the development or functioning of the immune system, an organismal system for calibrated responses to potential internal or invasive threats.
|
CD5L,
FCMR,
HP,
PTMS,
ADSS,
LRMP,
SQSTM1,
ADSSL1,
PIBF1,
NUDCD1,
TAPBPL
|
GO:0002377
|
BP
|
immunoglobulin production
|
The appearance of immunoglobulin due to biosynthesis or secretion following a cellular stimulus, resulting in an increase in its intracellular or extracellular levels.
|
ITM2A,
IL7R,
FAS
|
GO:0002378
|
BP
|
immunoglobulin biosynthetic process
|
The chemical reactions and pathways resulting in the formation of immunoglobulin.
|
PTPRC,
GALNT2
|
GO:0002381
|
BP
|
immunoglobulin production involved in immunoglobulin mediated immune response
|
The appearance of immunoglobulin due to biosynthesis or secretion following a cellular stimulus during an immune response, resulting in an increase in its intracellular or extracellular levels.
|
HLA-DQB1
|
GO:0002384
|
BP
|
hepatic immune response
|
An immune response taking place in the liver.
|
IL6,
IL6R
|
GO:0002385
|
BP
|
mucosal immune response
|
An immune response taking place in mucosal tissues, including those of the intestinal tract, nasal and upper respiratory tract, and genital tract.
|
OTUD7B
|
GO:0002399
|
BP
|
MHC class II protein complex assembly
|
The aggregation, arrangement and bonding together of a set of components to form an MHC class II protein complex.
|
HLA-DMB
|
GO:0002407
|
BP
|
dendritic cell chemotaxis
|
The movement of a dendritic cell in response to an external stimulus.
|
HMGB1,
CCL5,
CXCR2,
GPR183,
PIK3CG,
CXCR4,
ANO6,
TRPM4
|
GO:0002408
|
BP
|
myeloid dendritic cell chemotaxis
|
The movement of a myeloid dendritic cell in response to an external stimulus.
|
ARHGEF5
|
GO:0002418
|
BP
|
immune response to tumor cell
|
An immune system process that functions in the response of an organism to a tumor cell.
|
MICA
|
GO:0002429
|
BP
|
immune response-activating cell surface receptor signaling pathway
|
A series of molecular signals initiated by the binding of an extracellular ligand to a receptor on the surface of a cell capable of activating or perpetuating an immune response.
|
MICB
|
GO:0002430
|
BP
|
complement receptor mediated signaling pathway
|
A series of molecular signals generated as a consequence of a component of the complement pathway binding to a complement receptor. Such components include both whole complement proteins and fragments of complement proteins generated through the activity of the complement pathway.
|
GPR32,
CR1,
FPR1,
FPR2,
GPLD1
|
GO:0002431
|
BP
|
Fc receptor mediated stimulatory signaling pathway
|
A series of molecular signals generated as a consequence of a the binding of the Fc portion of an immunoglobulin by an Fc receptor capable of activating or perpetuating an immune response. The Fc portion of an immunoglobulin is its C-terminal constant region.
|
LYN
|
GO:0002432
|
BP
|
granuloma formation
|
The formation of nodular inflammatory lesions, usually small or granular, firm, persistent, well-structured, and containing compactly grouped T lymphocytes and modified phagocytes such as epithelioid cells, giant cells, and other macrophages. Granuloma formation represents a chronic inflammatory response initiated by various infectious and noninfectious agents. The center of a granuloma consists of fused macrophages, which can become necrotic.
|
CEBPB
|
GO:0002437
|
BP
|
inflammatory response to antigenic stimulus
|
An inflammatory response to an antigenic stimulus, which can be include any number of T cell or B cell epitopes.
|
HMGB1,
HMGB2,
NOTCH1,
IL5RA
|
GO:0002438
|
BP
|
acute inflammatory response to antigenic stimulus
|
An acute inflammatory response to an antigenic stimulus. An acute inflammatory response occurs within a matter of minutes or hours, and either resolves within a few days or becomes a chronic inflammatory response.
|
SERPINC1,
ICAM1,
CXCR2,
CD6
|
GO:0002439
|
BP
|
chronic inflammatory response to antigenic stimulus
|
A chronic inflammatory response to an antigenic stimulus. A chronic inflammatory response persists indefinitely during days, weeks, or months in the life of an individual.
|
TNF,
AHCY
|
GO:0002446
|
BP
|
neutrophil mediated immunity
|
Any process involved in the carrying out of an immune response by a neutrophil.
|
IL6,
ACE,
CXCL5,
ADAM17,
CXCL6,
KMT2E
|
GO:0002448
|
BP
|
mast cell mediated immunity
|
Any process involved in the carrying out of an immune response by a mast cell.
|
SERPINB9,
SPON2
|
GO:0002455
|
BP
|
humoral immune response mediated by circulating immunoglobulin
|
An immune response dependent upon secreted immunoglobulin. An example of this process is found in Mus musculus.
|
HLA-DQB1,
BCL3,
ZP3,
EXO1
|
GO:0002456
|
BP
|
T cell mediated immunity
|
Any process involved in the carrying out of an immune response by a T cell.
|
MYO1G,
BTN3A3,
CD46,
GNL1,
BTN3A2,
JAG1,
FOXP3
|
GO:0002457
|
BP
|
T cell antigen processing and presentation
|
The process in which a T cell expresses antigen (peptide or lipid) on its cell surface in association with an MHC protein complex.
|
ICAM1,
RFTN1
|
GO:0002460
|
BP
|
adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains
|
An immune response based on directed amplification of specific receptors for antigen produced through a somatic diversification process that includes somatic recombination of germline gene segments encoding immunoglobulin superfamily domains, and allowing for enhanced responses upon subsequent exposures to the same antigen (immunological memory). Recombined receptors for antigen encoded by immunoglobulin superfamily domains include T cell receptors and immunoglobulins (antibodies). An example of this is the adaptive immune response found in Mus musculus.
|
TGFB1
|
GO:0002467
|
BP
|
germinal center formation
|
The process in which germinal centers form. A germinal center is a specialized microenvironment formed when activated B cells enter lymphoid follicles. Germinal centers are the foci for B cell proliferation and somatic hypermutation.
|
BCL3,
BCL6,
ADAM17,
MEF2C,
KLHL6
|
GO:0002474
|
BP
|
antigen processing and presentation of peptide antigen via MHC class I
|
The process in which an antigen-presenting cell expresses a peptide antigen on its cell surface in association with an MHC class I protein complex. Class I here refers to classical class I molecules.
|
SEC24D,
SEC31A,
HLA-B,
ACE,
HLA-E,
HLA-G,
CALR,
CANX,
PDIA3,
HLA-A,
HLA-F,
BCAP31,
SEC13,
B2M,
SEC23A,
ERAP2,
MR1,
ERAP1,
SAR1B
|
GO:0002476
|
BP
|
antigen processing and presentation of endogenous peptide antigen via MHC class Ib
|
The process in which an antigen-presenting cell expresses a peptide antigen of endogenous origin on its cell surface in association with an MHC class Ib protein complex. The peptide is typically a fragment of a larger endogenous protein which has been degraded within the cell. Class Ib here refers to non-classical class I molecules, such as those of the HLA-E gene family.
|
HLA-E
|
GO:0002479
|
BP
|
antigen processing and presentation of exogenous peptide antigen via MHC class I, TAP-dependent
|
The process in which an antigen-presenting cell expresses a peptide antigen of exogenous origin on its cell surface in association with an MHC class I protein complex following intracellular transport via a TAP (transporter associated with antigen processing) pathway. The peptide is typically a fragment of a larger exogenous protein which has been degraded within the cell and is dependent on TAP transport from the cytosol to ER for association with the MHC class I molecule. Class I here refers to classical class I molecules.
|
PSMD11,
PSMD12,
PSMD3,
PSMD10,
HLA-B,
CYBB,
ITGAV,
FCGR1A,
HLA-E,
CD36,
HLA-G,
PSMC3,
ITGB5,
NCF2,
PSMB1,
PSMA1,
PSMA2,
PSMA3,
PSMA4,
PSMB8,
PSMB9,
PSMB4,
PSMB5,
HLA-A,
HLA-F,
PSMC2,
PSMB10,
PSMC4,
PSMB3,
PSMD7,
PSME3,
B2M,
PSMC1,
PSMC6,
PSMD2,
PSME4,
NCF4,
FCGR1B
|
GO:0002480
|
BP
|
antigen processing and presentation of exogenous peptide antigen via MHC class I, TAP-independent
|
The process in which an antigen-presenting cell expresses a peptide antigen of exogenous origin on its cell surface in association with an MHC class I protein complex following intracellular transport via a pathway not requiring TAP (transporter associated with antigen processing). The peptide is typically a fragment of a larger exogenous protein which has been degraded within the cell. Class I here refers to classical class I molecules.
|
HLA-B,
HLA-E,
HLA-G,
HLA-A,
HLA-F,
B2M,
LNPEP
|
GO:0002481
|
BP
|
antigen processing and presentation of exogenous protein antigen via MHC class Ib, TAP-dependent
|
The process in which an antigen-presenting cell expresses a peptide antigen of exogenous origin on its cell surface in association with an MHC class Ib protein complex following intracellular transport via a TAP (transporter associated with antigen processing) pathway. The peptide is typically a fragment of a larger exogenous protein which has been degraded within the cell and is dependent on TAP transport from the cytosol to ER for association with the MHC class Ib molecule. Class Ib here refers to non-classical class I molecules, such as those of the HLA-E gene family.
|
B2M
|
GO:0002495
|
BP
|
antigen processing and presentation of peptide antigen via MHC class II
|
The process in which an antigen-presenting cell expresses a peptide antigen on its cell surface in association with an MHC class II protein complex. The peptide antigen is typically, but not always, processed from a whole protein.
|
MARCH8,
MARCH1
|
GO:0002502
|
BP
|
peptide antigen assembly with MHC class I protein complex
|
The binding of a peptide to the antigen binding groove of an MHC class I protein complex. Class I here refers to classical class I molecules.
|
CALR
|
GO:0002503
|
BP
|
peptide antigen assembly with MHC class II protein complex
|
The binding of a peptide to the antigen binding groove of an MHC class II protein complex.
|
HLA-DRA,
HLA-DMB
|
GO:0002504
|
BP
|
antigen processing and presentation of peptide or polysaccharide antigen via MHC class II
|
The process in which an antigen-presenting cell expresses antigen (peptide or polysaccharide) on its cell surface in association with an MHC class II protein complex.
|
HLA-DRA
|
GO:0002506
|
BP
|
polysaccharide assembly with MHC class II protein complex
|
The binding of a polysaccharide to the antigen binding groove of an MHC class II protein complex.
|
HLA-DRA
|
GO:0002513
|
BP
|
tolerance induction to self antigen
|
Tolerance induction directed at self antigens.
|
TGFB1,
LYN,
FOXP3
|
GO:0002520
|
BP
|
immune system development
|
The process whose specific outcome is the progression of an organismal system whose objective is to provide calibrated responses by an organism to a potential internal or invasive threat, over time, from its formation to the mature structure. A system is a regularly interacting or interdependent group of organs or tissues that work together to carry out a given biological process.
|
TROVE2,
SMAD3,
CACNA1C
|
GO:0002521
|
BP
|
leukocyte differentiation
|
The process in which a relatively unspecialized hemopoietic precursor cell acquires the specialized features of a leukocyte. A leukocyte is an achromatic cell of the myeloid or lymphoid lineages capable of ameboid movement, found in blood or other tissue.
|
RRAS
|
GO:0002523
|
BP
|
leukocyte migration involved in inflammatory response
|
The movement of a leukocyte within or between different tissues and organs of the body contributing to an inflammatory response.
|
PPBP,
ITGB2,
S100A8,
S100A9,
CCL2,
SELE,
ADAM8,
JAM3
|
GO:0002526
|
BP
|
acute inflammatory response
|
Inflammation which comprises a rapid, short-lived, relatively uniform response to acute injury or antigenic challenge and is characterized by accumulations of fluid, plasma proteins, and granulocytic leukocytes. An acute inflammatory response occurs within a matter of minutes or hours, and either resolves within a few days or becomes a chronic inflammatory response.
|
PTGES,
NUPR1,
VNN1,
APOA2,
S100A8,
B4GALT1,
VCAM1,
TNFSF4,
ACVR1
|
GO:0002532
|
BP
|
production of molecular mediator involved in inflammatory response
|
The synthesis or release of any molecular mediator of the inflammatory response following an inflammatory stimulus, resulting in an increase in its intracellular or extracellular levels.
|
IL4R
|
GO:0002534
|
BP
|
cytokine production involved in inflammatory response
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The synthesis or release of a cytokine following a inflammatory stimulus as part of an inflammatory response, resulting in an increase in its intracellular or extracellular levels.
|
SEH1L
|
GO:0002537
|
BP
|
nitric oxide production involved in inflammatory response
|
The synthesis or release of nitric oxide following a stimulus as part of an inflammatory response, resulting in an increase in its intracellular or extracellular levels.
|
TLR4,
SLC7A2
|
GO:0002540
|
BP
|
leukotriene production involved in inflammatory response
|
The synthesis or release of any leukotriene following a stimulus as part of an inflammatory response, resulting in an increase in its intracellular or extracellular levels.
|
ALOX5
|
GO:0002543
|
BP
|
activation of blood coagulation via clotting cascade
|
Any process that initiates the clotting cascade of blood coagulation, a cascade of plasma enzymes that is triggered following damage to blood vessels, leading to formation of a clot.
|
ANO6
|
GO:0002544
|
BP
|
chronic inflammatory response
|
Inflammation of prolonged duration (weeks or months) in which active inflammation, tissue destruction, and attempts at repair are proceeding simultaneously. Although it may follow acute inflammation, chronic inflammation frequently begins insidiously, as a low-grade, smoldering, often asymptomatic response.
|
PTGES,
VNN1,
S100A8,
THBS1,
GJA1,
VCAM1
|
GO:0002548
|
BP
|
monocyte chemotaxis
|
The movement of a monocyte in response to an external stimulus.
|
TNFSF11,
PDGFB,
ANXA1,
IL6,
IL6R,
CCL3,
CCL4,
CCL2,
CCL5,
LGALS3,
CCL20,
CCL8,
PTPRO,
TNFRSF11A
|
GO:0002551
|
BP
|
mast cell chemotaxis
|
The movement of a mast cell in response to an external stimulus.
|
PIK3CD,
KIT,
RAC1
|
GO:0002553
|
BP
|
histamine secretion by mast cell
|
The regulated release of histamine by a mast cell or group of mast cells.
|
SNAP23,
LYN
|
GO:0002554
|
BP
|
serotonin secretion by platelet
|
The regulated release of serotonin by a platelet or group of platelets.
|
SYK
|
GO:0002573
|
BP
|
myeloid leukocyte differentiation
|
The process in which a relatively unspecialized myeloid precursor cell acquires the specialized features of any cell of the myeloid leukocyte lineage.
|
HHEX
|
GO:0002576
|
BP
|
platelet degranulation
|
The regulated exocytosis of secretory granules containing preformed mediators such as histamine and serotonin by a platelet.
|
ISLR,
ABCC4,
ACTN4,
WDR1,
PHACTR2,
F8,
F13A1,
PLG,
SERPINA1,
SERPINA3,
A2M,
TIMP1,
KNG1,
PDGFB,
TGFB1,
IGF2,
APOA1,
FGA,
FGB,
FGG,
APOH,
FN1,
ORM1,
AHSG,
ALB,
PPBP,
PF4,
TF,
ALDOA,
PDGFA,
A1BG,
VWF,
IGF1,
APP,
ITGB3,
SERPINE1,
SERPING1,
CLEC3B,
PSAP,
LYN,
THBS1,
SPARC,
SRGN,
CLU,
F5,
ACTN1,
LAMP2,
HGF,
VEGFA,
PECAM1,
CD36,
ORM2,
FLNA,
CD9,
ACTN2,
TIMP3,
VEGFB,
VEGFC,
SEPP1,
STXBP1,
TGFB2,
CALM2,
TMSB4X,
TUBA4A,
APLP2,
SPP2,
MMRN1,
GAS6,
HABP4,
TTN,
FAM3C,
RARRES2,
TLN1
|
GO:0002581
|
BP
|
negative regulation of antigen processing and presentation of peptide or polysaccharide antigen via MHC class II
|
Any process that stops, prevents, or reduces the frequency, rate, or extent of antigen processing and presentation of antigen (peptide or polysaccharide) via MHC class II.
|
THBS1
|
GO:0002587
|
BP
|
negative regulation of antigen processing and presentation of peptide antigen via MHC class II
|
Any process that stops, prevents, or reduces the frequency, rate, or extent of antigen processing and presentation of peptide antigen via MHC class II.
|
HLA-DOB
|
GO:0002588
|
BP
|
positive regulation of antigen processing and presentation of peptide antigen via MHC class II
|
Any process that activates or increases the frequency, rate, or extent of antigen processing and presentation of peptide antigen via MHC class II.
|
PYCARD
|