InnateDB Protein
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IDBP-584276.3
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Last Modified
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2014-10-13 [Report errors or provide feedback]
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Gene Symbol
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CD3G
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Protein Name
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CD3g molecule, gamma (CD3-TCR complex)
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Synonyms
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CD3-GAMMA; IMD17; T3G;
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Species
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Homo sapiens
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Ensembl Protein
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ENSP00000431445
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InnateDB Gene
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IDBG-73647 (CD3G)
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Protein Structure
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Function |
The CD3 complex mediates signal transduction.
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Subcellular Localization |
Membrane; Single-pass type I membrane protein.
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Disease Associations |
Immunodeficiency 17 (IMD17) [MIM:615607]: An autosomal recessive primary immunodeficiency characterized by highly variable clinical severity. Some patients have onset of severe recurrent infections in early infancy that may be lethal, whereas others may be only mildly affected or essentially asymptomatic into young adulthood. More severely affected patients may have evidence of autoimmune disease or enteropathy. The immunologic pattern is similar among patients, showing partial T-cell lymphopenia, decreased amounts of the CD3 complex, and impaired proliferative responses to T-cell receptor dependent stimuli. The phenotype in some patients is reminiscent of severe combined immunodeficiency. {ECO:0000269PubMed:1635567, ECO:0000269PubMed:17277165}. Note=The disease is caused by mutations affecting the gene represented in this entry.
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Tissue Specificity |
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Comments |
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Number of Interactions
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This gene and/or its encoded proteins are associated with 11 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated |
Total |
11
[view]
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Protein-Protein |
7
[view]
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Protein-DNA |
4
[view]
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Protein-RNA |
0
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DNA-DNA |
0
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RNA-RNA |
0
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DNA-RNA |
0
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Predicted by orthology |
Total |
1 [view]
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Molecular Function |
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Biological Process |
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Cellular Component |
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PDB ID |
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InterPro |
IPR003110
Phosphorylated immunoreceptor signalling ITAM
IPR003598
Immunoglobulin subtype 2
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PFAM |
PF02189
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PRINTS |
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PIRSF |
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SMART |
SM00077
SM00408
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TIGRFAMs |
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Modification |
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SwissProt |
P09693
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PhosphoSite |
PhosphoSite-P09693
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TrEMBL |
B0YIY5
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UniProt Splice Variant |
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Entrez Gene |
917
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UniGene |
Hs.2259
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RefSeq |
NP_000064
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HUGO |
HGNC:1675
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OMIM |
186740
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CCDS |
CCDS8395
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HPRD |
07037
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IMGT |
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EMBL |
AK313966
AK315895
BC113830
CH471065
EF444965
X04145
X06026
X06027
X06028
X06029
X06030
X06031
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GenPept |
AAI13831
ACA05963
BAF98786
BAG36681
CAA27764
CAA29428
EAW67368
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