Homo sapiens Gene: CLEC3B
Summary
InnateDB Gene IDBG-29452.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol CLEC3B
Gene Name C-type lectin domain family 3, member B
Synonyms TN; TNA;
Species Homo sapiens
Ensembl Gene ENSG00000163815
Encoded Proteins
C-type lectin domain family 3, member B
C-type lectin domain family 3, member B
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary Currently no Entrez Summary Available. You might want to check the Summary Sections of the Orthologs.
Gene Information
Type Protein coding
Genomic Location Chromosome 3:45001548-45036071
Strand Forward strand
Band p21.31
Transcripts
ENST00000296130 ENSP00000296130
ENST00000428034 ENSP00000396013
ENST00000490386
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 24 experimentally validated interaction(s) in this database.
Experimentally validated
Total 24 [view]
Protein-Protein 24 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005509 calcium ion binding
GO:0008201 heparin binding
GO:0030246 carbohydrate binding
GO:0036143 kringle domain binding
Biological Process
GO:0001501 skeletal system development
GO:0001503 ossification
GO:0010756 positive regulation of plasminogen activation
GO:0030282 bone mineralization
GO:0071310 cellular response to organic substance
GO:0071560 cellular response to transforming growth factor beta stimulus
Cellular Component
GO:0001652 granular component
GO:0005576 extracellular region
GO:0005615 extracellular space
GO:0005737 cytoplasm
GO:0031012 extracellular matrix
GO:0070062 extracellular vesicular exosome
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Method
Confidence
Comments
SSD Ortholog
Ortholog supports species divergence
Not yet available
SSD Ortholog
Ortholog supports species divergence
Cross-References
SwissProt
TrEMBL E9PHK0
UniProt Splice Variant
Entrez Gene 7123
UniGene
RefSeq XM_005265426 NM_003278
HUGO HGNC:11891
OMIM 187520
CCDS CCDS2726
HPRD 01759
IMGT
EMBL AC104165
GenPept
RNA Seq Atlas 7123