Summary | |
---|---|
Symbol | ARHGAP44 |
Name | Rho GTPase activating protein 44 |
Aliases | KIAA0672; RICH-2; RICH2; NPC-A-10; Rho-type GTPase-activating protein RICH2; RhoGAP interacting with CIP4 ho ...... |
Chromosomal Location | 17p12 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Basic function annotation. > Subcellular Location, Domain and Function > Gene Ontology > KEGG and Reactome Pathway |
Subcellular Location | Cell projection, dendritic spine Recycling endosome Cell junction, synapse Note=In CA1 hippocampal synapses, detected at both presynaptic and postsynaptic sites. |
Domain |
PF03114 BAR domain PF00620 RhoGAP domain |
Function |
GTPase-activating protein (GAP) that stimulates the GTPase activity of Rho-type GTPases. Thereby, controls Rho-type GTPases cycling between their active GTP-bound and inactive GDP-bound states. May act as a GAP for CDC42 and RAC1. Endosomal recycling protein which, in association with SHANK3, is involved in synaptic plasticity. Promotes GRIA1 exocytosis from recycling endosomes and spine morphological changes associated to long-term potentiation. |
Biological Process |
GO:0006887 exocytosis GO:0051056 regulation of small GTPase mediated signal transduction |
Molecular Function |
GO:0005096 GTPase activator activity GO:0005543 phospholipid binding GO:0008047 enzyme activator activity GO:0030695 GTPase regulator activity GO:0060589 nucleoside-triphosphatase regulator activity |
Cellular Component |
GO:0030425 dendrite GO:0031252 cell leading edge GO:0031256 leading edge membrane GO:0043197 dendritic spine GO:0044309 neuron spine GO:0055037 recycling endosome GO:0098794 postsynapse |
KEGG | - |
Reactome |
R-HSA-194840: Rho GTPase cycle R-HSA-162582: Signal Transduction R-HSA-194315: Signaling by Rho GTPases |
Summary | |
---|---|
Symbol | ARHGAP44 |
Name | Rho GTPase activating protein 44 |
Aliases | KIAA0672; RICH-2; RICH2; NPC-A-10; Rho-type GTPase-activating protein RICH2; RhoGAP interacting with CIP4 ho ...... |
Chromosomal Location | 17p12 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content | Literatures that report relations between ARHGAP44 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 | ARHGAP44 |
Name | Rho GTPase activating protein 44 |
Aliases | KIAA0672; RICH-2; RICH2; NPC-A-10; Rho-type GTPase-activating protein RICH2; RhoGAP interacting with CIP4 ho ...... |
Chromosomal Location | 17p12 |
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 ARHGAP44 in screening data sets for detecting immune reponses.
|
Summary | |
---|---|
Symbol | ARHGAP44 |
Name | Rho GTPase activating protein 44 |
Aliases | KIAA0672; RICH-2; RICH2; NPC-A-10; Rho-type GTPase-activating protein RICH2; RhoGAP interacting with CIP4 ho ...... |
Chromosomal Location | 17p12 |
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 ARHGAP44 in various data sets.
|
Points in the above scatter plot represent the mutation difference of ARHGAP44 in various data sets.
|
Summary | |
---|---|
Symbol | ARHGAP44 |
Name | Rho GTPase activating protein 44 |
Aliases | KIAA0672; RICH-2; RICH2; NPC-A-10; Rho-type GTPase-activating protein RICH2; RhoGAP interacting with CIP4 ho ...... |
Chromosomal Location | 17p12 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Relations between abundance of tumor-infiltrating lymphocytes (TILs) and expression, copy number, methylation, or mutation of ARHGAP44. 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 | ARHGAP44 |
Name | Rho GTPase activating protein 44 |
Aliases | KIAA0672; RICH-2; RICH2; NPC-A-10; Rho-type GTPase-activating protein RICH2; RhoGAP interacting with CIP4 ho ...... |
Chromosomal Location | 17p12 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Relations between three kinds of immunomodulators and expression, copy number, methylation, or mutation of ARHGAP44. These immunomo-dulators were collected from Charoentong's study. In this tab, users can examine which immunomodulators might be regulated by ARHGAP44. > Immunoinhibitor > Immunostimulator > MHC molecule |
Summary | |
---|---|
Symbol | ARHGAP44 |
Name | Rho GTPase activating protein 44 |
Aliases | KIAA0672; RICH-2; RICH2; NPC-A-10; Rho-type GTPase-activating protein RICH2; RhoGAP interacting with CIP4 ho ...... |
Chromosomal Location | 17p12 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Relations between chemokines (or receptors) and expression, copy number, methylation, or mutation of ARHGAP44. In this tab, users can examine which chemokines (or receptors) might be regulated by the current gene. > Chemokine > Receptor |
Summary | |
---|---|
Symbol | ARHGAP44 |
Name | Rho GTPase activating protein 44 |
Aliases | KIAA0672; RICH-2; RICH2; NPC-A-10; Rho-type GTPase-activating protein RICH2; RhoGAP interacting with CIP4 ho ...... |
Chromosomal Location | 17p12 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Distribution of ARHGAP44 expression across immune and molecular subtypes. > Immune subtype > Molecular subtype |
Summary | |
---|---|
Symbol | ARHGAP44 |
Name | Rho GTPase activating protein 44 |
Aliases | KIAA0672; RICH-2; RICH2; NPC-A-10; Rho-type GTPase-activating protein RICH2; RhoGAP interacting with CIP4 ho ...... |
Chromosomal Location | 17p12 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content |
Associations between ARHGAP44 and clinical features. > Overall survival analysis > Cancer stage > Tumor grade |
Summary | |
---|---|
Symbol | ARHGAP44 |
Name | Rho GTPase activating protein 44 |
Aliases | KIAA0672; RICH-2; RICH2; NPC-A-10; Rho-type GTPase-activating protein RICH2; RhoGAP interacting with CIP4 ho ...... |
Chromosomal Location | 17p12 |
External Links | HGNC, NCBI, Ensembl, Uniprot, GeneCards |
Content | Drugs targeting ARHGAP44 collected from DrugBank database. |
There is no record. |