MRC2 (mannose receptor C-type 2)
Gene | |
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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9902 |
Gene name
Gene Name - the full gene name approved by the HGNC.
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Mannose receptor C-type 2 |
Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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MRC2 |
Synonyms (NCBI Gene)
Gene synonyms aliases
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CD280, CLEC13E, ENDO180, UPARAP |
Chromosome
Chromosome number
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17 |
Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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17q23.2 |
Summary
Summary of gene provided in NCBI Entrez Gene.
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This gene encodes a member of the mannose receptor family of proteins that contain a fibronectin type II domain and multiple C-type lectin-like domains. The encoded protein plays a role in extracellular matrix remodeling by mediating the internalization a |
miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein | |||||||||||||||||||||||||||||||||||||||||||||||||||
UniProt ID | Q9UBG0 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Protein name | C-type mannose receptor 2 (C-type lectin domain family 13 member E) (Endocytic receptor 180) (Macrophage mannose receptor 2) (Urokinase-type plasminogen activator receptor-associated protein) (UPAR-associated protein) (Urokinase receptor-associated protei | ||||||||||||||||||||||||||||||||||||||||||||||||||
Protein function | May play a role as endocytotic lectin receptor displaying calcium-dependent lectin activity. Internalizes glycosylated ligands from the extracellular space for release in an endosomal compartment via clathrin-mediated endocytosis. May be involve | ||||||||||||||||||||||||||||||||||||||||||||||||||
PDB | 5AO5 , 5AO6 , 5E4K , 5E4L , 5EW6 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Family and domains |
Pfam
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Tissue specificity | TISSUE SPECIFICITY: Ubiquitous with low expression in brain, placenta, lung, kidney, pancreas, spleen, thymus and colon. Expressed in endothelial cells, fibroblasts and macrophages. Highly expressed in fetal lung and kidney. {ECO:0000269|PubMed:10683150, | ||||||||||||||||||||||||||||||||||||||||||||||||||
Sequence | |||||||||||||||||||||||||||||||||||||||||||||||||||
Sequence length | 1479 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Interactions | View interactions |
Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease information provided by ClinVar, GenCC, and GWAS databases.
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