Summary | |
---|---|
Symbol | AIM2 |
Name | absent in melanoma 2 |
Aliases | PYHIN4; Interferon-inducible protein AIM2 |
Chromosomal Location | 1q22 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Basic function annotation. > Subcellular Location, Domain and Function > Gene Ontology > KEGG and Reactome Pathway |
Subcellular Location | Nucleus. Cytoplasm. Note=Activated inflammasomes can aggregate in the cytosol as speck-like particles. |
Domain |
PF02760 HIN-200/IF120x domain PF02758 PAAD/DAPIN/Pyrin domain |
Function |
Involved in innate immune response by recognizing cytosolic double-stranded DNA and inducing caspase-1-activating inflammasome formation in macrophages. Upon binding to DNA is thought to undergo oligomerization and to associate with PYCARD initiating the recruitment of caspase-1 precusrsor and processing of interleukin-1 beta and interleukin-18. Detects cytosolic dsDNA of viral and bacterial origin in a non-sequence-specific manner. Can also trigger PYCARD-dependent, caspase-1-independent cell death that involves caspase-8 (By similarity). Tumor suppressor which may act by repressing NF-kappa-B transcriptional activity. |
Biological Process |
GO:0001819 positive regulation of cytokine production GO:0002218 activation of innate immune response GO:0002230 positive regulation of defense response to virus by host GO:0002697 regulation of immune effector process GO:0002831 regulation of response to biotic stimulus GO:0009306 protein secretion GO:0009615 response to virus GO:0010950 positive regulation of endopeptidase activity GO:0010952 positive regulation of peptidase activity GO:0031334 positive regulation of protein complex assembly GO:0031349 positive regulation of defense response GO:0032088 negative regulation of NF-kappaB transcription factor activity GO:0032459 regulation of protein oligomerization GO:0032461 positive regulation of protein oligomerization GO:0032611 interleukin-1 beta production GO:0032612 interleukin-1 production GO:0032651 regulation of interleukin-1 beta production GO:0032652 regulation of interleukin-1 production GO:0032731 positive regulation of interleukin-1 beta production GO:0032732 positive regulation of interleukin-1 production GO:0033209 tumor necrosis factor-mediated signaling pathway GO:0034612 response to tumor necrosis factor GO:0035456 response to interferon-beta GO:0035458 cellular response to interferon-beta GO:0035690 cellular response to drug GO:0042493 response to drug GO:0043254 regulation of protein complex assembly GO:0043433 negative regulation of sequence-specific DNA binding transcription factor activity GO:0043900 regulation of multi-organism process GO:0043903 regulation of symbiosis, encompassing mutualism through parasitism GO:0044089 positive regulation of cellular component biogenesis GO:0045088 regulation of innate immune response GO:0045089 positive regulation of innate immune response GO:0045862 positive regulation of proteolysis GO:0050663 cytokine secretion GO:0050688 regulation of defense response to virus GO:0050691 regulation of defense response to virus by host GO:0050701 interleukin-1 secretion GO:0050702 interleukin-1 beta secretion GO:0050704 regulation of interleukin-1 secretion GO:0050706 regulation of interleukin-1 beta secretion GO:0050707 regulation of cytokine secretion GO:0050708 regulation of protein secretion GO:0050714 positive regulation of protein secretion GO:0050715 positive regulation of cytokine secretion GO:0050716 positive regulation of interleukin-1 secretion GO:0050718 positive regulation of interleukin-1 beta secretion GO:0050792 regulation of viral process GO:0051047 positive regulation of secretion GO:0051090 regulation of sequence-specific DNA binding transcription factor activity GO:0051091 positive regulation of sequence-specific DNA binding transcription factor activity GO:0051092 positive regulation of NF-kappaB transcription factor activity GO:0051222 positive regulation of protein transport GO:0051259 protein oligomerization GO:0051607 defense response to virus GO:0052547 regulation of peptidase activity GO:0052548 regulation of endopeptidase activity GO:0070269 pyroptosis GO:0071356 cellular response to tumor necrosis factor GO:0098542 defense response to other organism GO:1903532 positive regulation of secretion by cell GO:1904951 positive regulation of establishment of protein localization GO:2000116 regulation of cysteine-type endopeptidase activity GO:2001056 positive regulation of cysteine-type endopeptidase activity |
Molecular Function | - |
Cellular Component |
GO:0044445 cytosolic part GO:0061702 inflammasome complex GO:0097169 AIM2 inflammasome complex |
KEGG |
hsa04621 NOD-like receptor signaling pathway hsa04623 Cytosolic DNA-sensing pathway |
Reactome |
R-HSA-168256: Immune System R-HSA-622312: Inflammasomes R-HSA-168249: Innate Immune System R-HSA-168643: Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways R-HSA-844615: The AIM2 inflammasome |
Summary | |
---|---|
Symbol | AIM2 |
Name | absent in melanoma 2 |
Aliases | PYHIN4; Interferon-inducible protein AIM2 |
Chromosomal Location | 1q22 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content | Literatures that report relations between AIM2 and anti-tumor immunity. The specific mechanism were also collected if the literature reports that a gene specifically promotes or inhibits the infiltration or function of T/NK cells. |
There is no record. |
Summary | |
---|---|
Symbol | AIM2 |
Name | absent in melanoma 2 |
Aliases | PYHIN4; Interferon-inducible protein AIM2 |
Chromosomal Location | 1q22 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content | High-throughput screening data (e.g. CRISPR-Cas9, shRNA and RNAi) for T cell-mediated killing. Genetic screen techniques can identify mechanisms of tumor cell resistance (e.g., PTPN2) and sensitivity (e.g., APLNR) to killing by cytotoxic T cells, the central effectors of anti-tumor immunity. After comprehensively searching, eight groups of screening data sets were collected in the current database. In this tab, users can check whether their selected genes cause resistance or increase sensitivity to T cell-mediated killing in various data sets. |
> High-throughput Screening
[ TOP ]
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Statistical results of AIM2 in screening data sets for detecting immune reponses.
|
Summary | |
---|---|
Symbol | AIM2 |
Name | absent in melanoma 2 |
Aliases | PYHIN4; Interferon-inducible protein AIM2 |
Chromosomal Location | 1q22 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Transcriptomic and genomic profiling of pre-treated tumor biopsies from responders and non-responders to immunotherapy. These data were used to identify signatures and mechanisms of response to checkpoint blockade (e.g., anti-PDL1 and anti-PD1). One example is that mutations in the gene PBRM1 benefit clinical survival of patients with clear cell renal cell carcinoma. After comprehensively searching, we collected 5 and 6 of transcriptomic and genomic data sets, respectively. In this tab, users can check whether their selected genes have significant difference of expression or mutation between responders and non-responders in various data sets. > Expression difference between responders and non-responders > Mutation difference between responders and non-responders |
Points in the above scatter plot represent the expression difference of AIM2 in various data sets.
|
Points in the above scatter plot represent the mutation difference of AIM2 in various data sets.
|
Summary | |
---|---|
Symbol | AIM2 |
Name | absent in melanoma 2 |
Aliases | PYHIN4; Interferon-inducible protein AIM2 |
Chromosomal Location | 1q22 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Relations between abundance of tumor-infiltrating lymphocytes (TILs) and expression, copy number, methylation, or mutation of AIM2. The immune-related signatures of 28 TIL types from Charoentong's study, which can be viewed in the download page. For each cancer type, the relative abundance of TILs were inferred by using gene set variation analysis (GSVA) based on gene expression profile. In this tab, users can examine which kinds of TILs might be regulated by the current gene. |
Summary | |
---|---|
Symbol | AIM2 |
Name | absent in melanoma 2 |
Aliases | PYHIN4; Interferon-inducible protein AIM2 |
Chromosomal Location | 1q22 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Relations between three kinds of immunomodulators and expression, copy number, methylation, or mutation of AIM2. These immunomo-dulators were collected from Charoentong's study. In this tab, users can examine which immunomodulators might be regulated by AIM2. > Immunoinhibitor > Immunostimulator > MHC molecule |
Summary | |
---|---|
Symbol | AIM2 |
Name | absent in melanoma 2 |
Aliases | PYHIN4; Interferon-inducible protein AIM2 |
Chromosomal Location | 1q22 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Relations between chemokines (or receptors) and expression, copy number, methylation, or mutation of AIM2. In this tab, users can examine which chemokines (or receptors) might be regulated by the current gene. > Chemokine > Receptor |
Summary | |
---|---|
Symbol | AIM2 |
Name | absent in melanoma 2 |
Aliases | PYHIN4; Interferon-inducible protein AIM2 |
Chromosomal Location | 1q22 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Distribution of AIM2 expression across immune and molecular subtypes. > Immune subtype > Molecular subtype |
Summary | |
---|---|
Symbol | AIM2 |
Name | absent in melanoma 2 |
Aliases | PYHIN4; Interferon-inducible protein AIM2 |
Chromosomal Location | 1q22 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Associations between AIM2 and clinical features. > Overall survival analysis > Cancer stage > Tumor grade |