InnateDB Protein
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IDBP-366750.3
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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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CLEC2A
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Protein Name
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C-type lectin domain family 2, member A
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Synonyms
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Species
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Homo sapiens
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Ensembl Protein
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ENSP00000396163
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InnateDB Gene
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IDBG-18208 (CLEC2A)
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Protein Structure
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Function |
Plays a role in modulating the extent of T-cell expansion. Enhances the expansion of TCR-stimulated T-cells by increasing their survival through enhanced expression of anti- apoptotic proteins. May modulate the capacity of T-cells to home to lymph nodes through SELL. Facilitates dedicated immune recognition of keratinocytes via interaction with its receptor KLRF2 by stimulating natural killer cell mediated cytotoxicity. {ECO:0000269PubMed:18550855, ECO:0000269PubMed:20194751}.
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Subcellular Localization |
Cell membrane {ECO:0000269PubMed:18046548, ECO:0000269PubMed:18550855}; Single-pass type II membrane protein {ECO:0000269PubMed:18046548, ECO:0000269PubMed:18550855}.
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Disease Associations |
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Tissue Specificity |
Mainly expressed in skin. Also expressed in keratinocytes, spleen, thymus, small intestine, peripheral blood monocytes, bone marrow, ovary, testis and skin. High expression in CD8(+), B-lymphocytes and naive CD4(+) T-cells. Restricted mostly to proliferating lymphocytes. Not detected in myeloid leukocytes or natural killer (NK) cells. {ECO:0000269PubMed:18046548, ECO:0000269PubMed:18550855, ECO:0000269PubMed:20194751}.
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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 1 experimentally validated interaction(s) in this database.
Experimentally validated |
Total |
1
[view]
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Protein-Protein |
1
[view]
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Protein-DNA |
0
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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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Molecular Function |
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Biological Process |
GO:0042267
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natural killer cell mediated cytotoxicity
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Cellular Component |
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PDB ID |
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InterPro |
IPR001304
C-type lectin
IPR016187
C-type lectin fold
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PFAM |
PF00059
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PRINTS |
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PIRSF |
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SMART |
SM00034
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TIGRFAMs |
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Modification |
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SwissProt |
Q6UVW9
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PhosphoSite |
PhosphoSite-
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TrEMBL |
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UniProt Splice Variant |
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Entrez Gene |
387836
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UniGene |
Hs.527665
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RefSeq |
NP_001124183
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HUGO |
HGNC:24191
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OMIM |
612087
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CCDS |
CCDS44829
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HPRD |
16720
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IMGT |
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EMBL |
AY359126
EF127467
EU095393
EU095394
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GenPept |
AAQ89483
ABO33172
ABW79912
ABW79913
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