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RAP1A and RASGRP4
Number of citations of the paper that reports this interaction (PubMedID
11880369
)
36
Data Source:
HPRD
(in vitro)
RAP1A
RASGRP4
Description
RAP1A, member of RAS oncogene family
RAS guanyl releasing protein 4
Image
GO Annotations
Cellular Component
Cytoplasm
Early Endosome
Late Endosome
Cytosol
Plasma Membrane
Endosome Membrane
Cell Junction
Guanyl-nucleotide Exchange Factor Complex
Specific Granule Membrane
Neuron Projection
Phagocytic Vesicle
Perinuclear Region Of Cytoplasm
Extracellular Exosome
Glutamatergic Synapse
Nucleoplasm
Cytosol
Plasma Membrane
Membrane
Molecular Function
GTPase Activity
G Protein Activity
Guanyl-nucleotide Exchange Factor Activity
Protein Binding
GTP Binding
GDP Binding
Small GTPase Binding
Protein-containing Complex Binding
Guanyl-nucleotide Exchange Factor Activity
Calcium Ion Binding
Diacylglycerol Binding
GTP-dependent Protein Binding
Biological Process
Nervous System Development
Response To Carbohydrate
Positive Regulation Of Neuron Projection Development
Microvillus Assembly
Rap Protein Signal Transduction
Negative Regulation Of Collagen Biosynthetic Process
Nerve Growth Factor Signaling Pathway
Positive Regulation Of GTPase Activity
Positive Regulation Of Protein Kinase Activity
Positive Regulation Of Glucose Import
Establishment Of Endothelial Barrier
Positive Regulation Of ERK1 And ERK2 Cascade
Cellular Response To CAMP
Cellular Response To Xenobiotic Stimulus
Protein Localization To Plasma Membrane
Response To Antineoplastic Agent
Liver Regeneration
Regulation Of Neurotransmitter Receptor Localization To Postsynaptic Specialization Membrane
Regulation Of Cell Junction Assembly
Positive Regulation Of Fc-gamma Receptor Signaling Pathway Involved In Phagocytosis
Cellular Response To Nerve Growth Factor Stimulus
Negative Regulation Of Synaptic Vesicle Exocytosis
Positive Regulation Of Vasculogenesis
Transmembrane Receptor Protein Tyrosine Kinase Signaling Pathway
Activation Of Phospholipase C Activity
Small GTPase Mediated Signal Transduction
Regulation Of G Protein-coupled Receptor Signaling Pathway
Cell Population Proliferation
Response To Extracellular Stimulus
Myeloid Cell Differentiation
Positive Regulation Of Ras Protein Signal Transduction
Pathways
Frs2-mediated activation
Frs2-mediated activation
ARMS-mediated activation
ARMS-mediated activation
Integrin signaling
GRB2:SOS provides linkage to MAPK signaling for Integrins
p130Cas linkage to MAPK signaling for integrins
Glucagon-like Peptide-1 (GLP1) regulates insulin secretion
Rap1 signalling
MAP2K and MAPK activation
Neutrophil degranulation
Signaling by moderate kinase activity BRAF mutants
Signaling by high-kinase activity BRAF mutants
Signaling by BRAF and RAF1 fusions
Paradoxical activation of RAF signaling by kinase inactive BRAF
MET activates RAP1 and RAC1
Signaling downstream of RAS mutants
Signaling by RAF1 mutants
FCERI mediated NF-kB activation
RAF/MAP kinase cascade
Drugs
Diseases
GWAS
Cognitive ability, years of educational attainment or schizophrenia (pleiotropy) (
31374203
)
Crohn's disease (
30500874
32581322
)
High altitude adaptation (
28373541
)
Lymphocyte counts (
32888494
)
Osteoporosis-related phenotypes (
20548944
)
Basophil count (
32888494
)
Basophil percentage of white cells (
32888494
)
Diisocyanate-induced asthma (
25918132
)
Eosinophil counts (
32888494
27863252
)
Eosinophil percentage of white cells (
32888494
27863252
)
Monocyte count (
32888494
)
Neutrophil percentage of granulocytes (
27863252
)
Sum eosinophil basophil counts (
27863252
)
Interacting Genes
43 interacting genes:
AFDN
APBB1IP
ARHGEF1
BIN1
BMX
BRAF
ELOA
FADD
FAF1
FAS
GABARAPL2
GANAB
HDAC1
HSPA1A
HSPA4
KRIT1
MTNR1A
NTRK1
PDE6D
PPP2R1A
PRKACA
RABAC1
RAF1
RALGDS
RAP1GAP
RAP1GDS1
RAPGEF1
RAPGEF2
RAPGEF3
RAPGEF4
RAPGEF5
RAPGEF6
RASA1
RASA3
RASGRP2
RASGRP4
RASIP1
RGL4
RGS14
RUNDC3A
SMARCA2
SMARCA4
TNFRSF10C
6 interacting genes:
BNIP2
DYNLL1
HRAS
RAP1A
SEC22A
TMPRSS4
Entrez ID
5906
115727
HPRD ID
01545
09540
Ensembl ID
ENSG00000116473
ENSG00000171777
Uniprot IDs
A8KAH9
P62834
Q8TDF6
PDB IDs
1C1Y
1GUA
3KUC
4KVG
6AXG
Enriched GO Terms of Interacting Partners
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