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CD3D and CD8A
Data Source:
HPRD
(in vitro, in vivo)
CD3D
CD8A
Description
CD3d molecule
CD8a molecule
Image
GO Annotations
Cellular Component
Cytoplasm
Plasma Membrane
External Side Of Plasma Membrane
Integral Component Of Membrane
Clathrin-coated Vesicle Membrane
T Cell Receptor Complex
Alpha-beta T Cell Receptor Complex
Extracellular Region
Plasma Membrane
Integral Component Of Plasma Membrane
External Side Of Plasma Membrane
T Cell Receptor Complex
Plasma Membrane Raft
Molecular Function
Transmembrane Signaling Receptor Activity
Protein Binding
Identical Protein Binding
Protein Heterodimerization Activity
Protein Binding
Coreceptor Activity
MHC Class I Protein Complex Binding
MHC Class I Protein Binding
Biological Process
Adaptive Immune Response
Cell Surface Receptor Signaling Pathway
Positive Thymic T Cell Selection
Regulation Of Immune Response
T Cell Receptor Signaling Pathway
Membrane Organization
T Cell Mediated Immunity
Immune Response
Cell Surface Receptor Signaling Pathway
Transmembrane Receptor Protein Tyrosine Kinase Signaling Pathway
Antigen Processing And Presentation
T Cell Activation
Cytotoxic T Cell Differentiation
Regulation Of Immune Response
Pathways
Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell
Downstream TCR signaling
Phosphorylation of CD3 and TCR zeta chains
Translocation of ZAP-70 to Immunological synapse
Generation of second messenger molecules
PD-1 signaling
Cargo recognition for clathrin-mediated endocytosis
Clathrin-mediated endocytosis
Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell
Drugs
Muromonab
Blinatumomab
Diseases
T-B+Severe combined immunodeficiencies (SCIDs), including the following eight diseases: X-linked SCID; Janus kinase-3 (Jak3) deficiency; IL-7 receptor alpha (IL7R alpha) deficiency; IL-2 receptor alpha (IL2R alpha) deficiency; CD45 deficiency; CD3 deficiency; Winged Helix Nude (WHN) deficiency; Immunodeficiency with thynoma
Combined immunodeficiencies (CIDs), including the following nine diseases: X-linked hyper IgM syndrome; CD40 deficiency hyper IgM syndrome; Purine nucleoside phosphorylase (PNP) deficiency; Omenn syndrome; MHC deficiency (HLA-class I); MHC deficiency (HLA-class II); Zap-70 deficiency; p56 Lck deficiency; CD8 deficiency
GWAS
Pulse pressure (
27841878
)
Blood protein levels (
30072576
)
Interacting Genes
12 interacting genes:
AP2M1
CANX
CD247
CD3E
CD3G
CD8A
CD8B
HERPUD1
KCNA3
SGTB
TRA
TRB
17 interacting genes:
B2M
CACYBP
CD3D
CD59
CD8B
CDK1
HLA-A
HLA-B
HLA-C
HLA-E
HLA-G
LAT
LCK
LGALS1
PTPRC
SREK1
SRSF1
Entrez ID
915
925
HPRD ID
01730
01737
Ensembl ID
ENSG00000167286
ENSG00000153563
Uniprot IDs
B0YIY4
P04234
P01732
Q6ZVS2
Q8TAW8
PDB IDs
1XIW
6JXR
1AKJ
1CD8
1Q69
2HP4
3QZW
Enriched GO Terms of Interacting Partners
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Tagcloud (Difference)
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Tagcloud (Intersection)
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