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GFAP and CRYAB
Data Source:
BioGRID
(pull down)
GFAP
CRYAB
Description
glial fibrillary acidic protein
crystallin alpha B
Image
GO Annotations
Cellular Component
Cytoplasm
Lysosome
Cytosol
Intermediate Filament
Intermediate Filament Cytoskeleton
Nucleus
Nucleoplasm
Cytoplasm
Mitochondrion
Golgi Apparatus
Cytosol
Cell Surface
Postsynaptic Density
Microtubule Cytoskeleton
Z Disc
Axon
M Band
Actin Filament Bundle
Protein-containing Complex
Dendritic Spine
Perikaryon
Extracellular Exosome
Synaptic Membrane
Cardiac Myofibril
Molecular Function
Structural Constituent Of Cytoskeleton
Protein Binding
Identical Protein Binding
Amyloid-beta Binding
Structural Molecule Activity
Structural Constituent Of Eye Lens
Protein Binding
Microtubule Binding
Identical Protein Binding
Protein Homodimerization Activity
Protein-containing Complex Binding
Metal Ion Binding
Unfolded Protein Binding
Biological Process
Regulation Of Protein-containing Complex Assembly
Intermediate Filament Organization
Regulation Of Chaperone-mediated Autophagy
Response To Hypoxia
Lens Development In Camera-type Eye
Protein Folding
Muscle Contraction
Tubulin Complex Assembly
Muscle Organ Development
Multicellular Organism Aging
Regulation Of Cell Death
Negative Regulation Of Cell Growth
Microtubule Polymerization Or Depolymerization
Negative Regulation Of Protein-containing Complex Assembly
Response To Estradiol
Negative Regulation Of Intracellular Transport
Response To Hydrogen Peroxide
Negative Regulation Of Apoptotic Process
Negative Regulation Of Cysteine-type Endopeptidase Activity Involved In Apoptotic Process
Negative Regulation Of Transcription, DNA-templated
Protein Stabilization
Stress-activated MAPK Cascade
Apoptotic Process Involved In Morphogenesis
Cellular Response To Gamma Radiation
Regulation Of Cellular Response To Heat
Negative Regulation Of Amyloid Fibril Formation
Negative Regulation Of Reactive Oxygen Species Metabolic Process
Pathways
Nuclear signaling by ERBB4
Chaperone Mediated Autophagy
HSF1-dependent transactivation
Drugs
Diseases
Alexander disease
Distal muscular dystrophies, including: Welander distal myopathy (WDM); Tibial muscular dystrophy (TMD); Nonaka distal myopathy with rimmed vacuoles (DMRV); Miyoshi myopathy (MM); Laing myopathy (MPD1); Distal nebulin myopathy (DNM); Distal desminopathy (MFM1); alpha-B Crystallinopathy (MFM2); Distal myotilinopathy (MFM3); Distal zaspopathy (MFM4); Distal myopathy 3 (MPD2, VCPDM)
Myofibrillar myopathies (MFM), including: Desminopathy (MFM1); alpha-B Crystallinopathy (MFM2); Myotilinopathy (MFM3); Zaspopathy (MFM4); Filaminopathy (MFM5); Bag3opathy
GWAS
Asthma (
31619474
)
Cognitive function (
25644384
)
Craniofacial microsomia (
26853712
)
Birth weight (
31043758
)
PR interval (
32439900
)
Interacting Genes
80 interacting genes:
ABI2
AKT1
APP
AURKB
BIRC2
CAMK2A
CARD10
CCDC57
CDC37
CDK1
CEP76
CFAP206
CRYAB
CT55
CWF19L2
DES
ENKD1
EPM2AIP1
FAM50B
GOLGA2
GRAP2
HGS
HOMEZ
IKBKG
KIAA0408
KRT13
KRT15
KRT19
KRT27
KRT31
KRT39
LENG1
LGALS14
LMO2
MAPK9
MEN1
MOS
MYBPHL
MYO15B
NEFL
NEK6
NFKBID
NTAQ1
NXF1
PDLIM1
PDLIM7
PDZK1
PIAS2
PIH1D2
POM121
PPP1R16B
PPP1R18
PRKACA
PRKCA
PRKCG
PSEN1
PSEN2
RIBC2
ROCK1
RORA
S100A1
S100B
SH3YL1
SMARCB1
SRC
STAT1
TBC1D21
TBC1D22B
TFIP11
TLE5
TP53BP2
TRIM27
TUBGCP4
UBASH3A
UBE3A
VIM
YES1
ZC2HC1C
ZNF655
ZNF774
54 interacting genes:
ACOT7
APOC2
APP
AVP
B2M
BAG3
BCL2L1
BMPR2
CAPN3
CASP3
CCL22
CCND1
CRYAA
CRYAA2
CRYBA1
CRYBB2
CRYGC
CRYGD
CRYGS
CS
DDX20
DES
EPB41
FCGR2A
FGF2
GFAP
GORASP2
HBA1
HSPB1
HSPB2
HSPB6
HSPB8
INS
KRTAP19-5
KRTAP6-1
KRTAP8-1
LALBA
MDH2
MIP
MRPL11
NGF
PRKAG3
PRNP
PSMA3
SCN5A
SLC13A1
SNCA
SOD1
SQSTM1
TNPO2
TRAPPC6A
TTN
UBE2D1
VEGFA
Entrez ID
2670
1410
HPRD ID
00675
00428
Ensembl ID
ENSG00000131095
ENSG00000109846
Uniprot IDs
A7REI1
P14136
A0A024R3B9
P02511
V9HW27
PDB IDs
6A9P
2KLR
2N0K
2WJ7
2Y1Y
2Y1Z
2Y22
2YGD
3J07
3L1G
3SGM
3SGN
3SGO
3SGP
3SGR
3SGS
4M5S
4M5T
5VVV
6BP9
Enriched GO Terms of Interacting Partners
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Tagcloud (Intersection)
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