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KRIT1 and TRPV4
Number of citations of the paper that reports this interaction (PubMedID
12724311
)
74
Data Source:
BioGRID
(unspecified method)
KRIT1
TRPV4
Description
KRIT1 ankyrin repeat containing
transient receptor potential cation channel subfamily V member 4
Image
GO Annotations
Cellular Component
Extracellular Space
Cell
Cytoplasm
Cytoskeleton
Plasma Membrane
Cell-cell Junction
Cell
Endoplasmic Reticulum
Cytoplasmic Microtubule
Plasma Membrane
Integral Component Of Plasma Membrane
Adherens Junction
Focal Adhesion
Cilium
Cell Surface
Integral Component Of Membrane
Apical Plasma Membrane
Lamellipodium
Filopodium
Growth Cone
Cortical Actin Cytoskeleton
Cytoplasmic Vesicle
Ruffle Membrane
Molecular Function
Protein Binding
Phosphatidylinositol-4,5-bisphosphate Binding
Microtubule Binding
GTPase Regulator Activity
Actin Binding
Osmosensor Activity
Protein Kinase C Binding
Ion Channel Activity
Cation Channel Activity
Calcium Channel Activity
Protein Binding
Calmodulin Binding
ATP Binding
Microtubule Binding
Lipid Binding
Stretch-activated, Cation-selective, Calcium Channel Activity
Protein Kinase Binding
SH2 Domain Binding
Identical Protein Binding
Alpha-tubulin Binding
Metal Ion Binding
Beta-tubulin Binding
Actin Filament Binding
Biological Process
Angiogenesis
Negative Regulation Of Endothelial Cell Proliferation
Small GTPase Mediated Signal Transduction
Negative Regulation Of Endothelial Cell Migration
Negative Regulation Of Angiogenesis
Cell Redox Homeostasis
Regulation Of Catalytic Activity
Regulation Of Establishment Of Cell Polarity
Negative Regulation Of Endothelial Cell Apoptotic Process
Negative Regulation Of Transcription By RNA Polymerase II
Diet Induced Thermogenesis
Calcium Ion Transport
Cellular Calcium Ion Homeostasis
Cell Volume Homeostasis
Actin Filament Organization
Cell-cell Junction Assembly
Positive Regulation Of Cytosolic Calcium Ion Concentration
Osmosensory Signaling Pathway
Response To Mechanical Stimulus
Positive Regulation Of Gene Expression
Positive Regulation Of Macrophage Chemotaxis
Negative Regulation Of Neuron Projection Development
Vasopressin Secretion
Positive Regulation Of Microtubule Depolymerization
Actin Cytoskeleton Reorganization
Response To Insulin
Cellular Response To Heat
Hyperosmotic Salinity Response
Glucose Homeostasis
Positive Regulation Of Vascular Permeability
Cortical Microtubule Organization
Positive Regulation Of JNK Cascade
Microtubule Polymerization
Regulation Of Response To Osmotic Stress
Positive Regulation Of Inflammatory Response
Multicellular Organismal Water Homeostasis
Cartilage Development Involved In Endochondral Bone Morphogenesis
Positive Regulation Of ERK1 And ERK2 Cascade
Calcium Ion Import
Calcium Ion Transmembrane Transport
Cellular Response To Osmotic Stress
Cellular Hypotonic Response
Cellular Hypotonic Salinity Response
Positive Regulation Of Monocyte Chemotactic Protein-1 Production
Positive Regulation Of Macrophage Inflammatory Protein 1 Alpha Production
Positive Regulation Of Chemokine (C-C Motif) Ligand 5 Production
Energy Homeostasis
Blood Vessel Endothelial Cell Delamination
Calcium Ion Import Into Cytosol
Negative Regulation Of Brown Fat Cell Differentiation
Signal Transduction Involved In Regulation Of Aerobic Respiration
Positive Regulation Of Chemokine (C-X-C Motif) Ligand 1 Production
Positive Regulation Of Interleukin-6 Secretion
Pathways
TRP channels
Drugs
Diseases
Cerebral cavernous malformation
Spinal muscular atrophy (SMA), including: SMA type I (SMA1) / Werdning-Hoffman disease; SMA type II (SMA2); SMA type III (SMA3) / Kugeleberg-Welander disease; SMA type IV (SMA4); X-linked SMA 2 (SMAX2); X-linked distal SMA 3 (DSMAX); Distal SMA autosomal recessive type 4 (DSMA4); Congenital distal spinal muscular atrophy (SMAL); SMA proximal adult autosomal dominant (SMAPAD)
TRPV4-related skeletal dysplasias, including: Autosomal dominant brachyolmia; Spondylometaphyseal dysplasia, Kozlowski type (SMDK); Metatropic dysplasia; Spondyloepiphyseal dysplasia, Maroteaux type ; Parastremmatic dysplasia
TRPV4-related peripheral neuropathies, including: Congenital distal spinal muscular atrophy (CDSMA); Scapuloperoneal spinal muscle atrophy (SPSMA); Hereditary motor and sensory neuropathy type IIC (HMSN IIC)
Distal hereditary motor neuropathies (dHMN)
GWAS
Coffee consumption (
31046077
)
Hippocampal volume in Alzheimer's disease dementia (
29274321
)
Creatinine levels (
29403010
)
Glomerular filtration rate (
29403010
)
Interacting Genes
6 interacting genes:
FAS
ITGB1BP1
PLCB3
RAP1A
RGS4
TRPV4
14 interacting genes:
CALM1
FYN
HCK
ITCH
KRIT1
LCK
LYN
MAP7
OS9
PACSIN1
PACSIN2
PACSIN3
SRC
YES1
Entrez ID
889
59341
HPRD ID
05020
05667
Ensembl ID
ENSG00000001631
ENSG00000111199
Uniprot IDs
A4D1F7
O00522
Q9HBA0
PDB IDs
3U7D
4DX8
4DXA
4HDO
4HDQ
4JIF
4TKN
5D68
4DX1
4DX2
Enriched GO Terms of Interacting Partners
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Tagcloud (Intersection)
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