Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
9902
Gene name Gene Name - the full gene name approved by the HGNC.
Mannose receptor C-type 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MRC2
Synonyms (NCBI Gene) Gene synonyms aliases
CD280, CLEC13E, ENDO180, UPARAP
Chromosome Chromosome number
17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17q23.2
Summary Summary of gene provided in NCBI Entrez Gene.
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.
miRTarBase ID miRNA Experiments Reference
MIRT001355 hsa-miR-1-3p pSILAC 18668040
MIRT001355 hsa-miR-1-3p Proteomics;Other 18668040
MIRT051126 hsa-miR-16-5p CLASH 23622248
MIRT047526 hsa-miR-10a-5p CLASH 23622248
MIRT1157632 hsa-miR-2355-5p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001649 Process Osteoblast differentiation HDA 16210410
GO:0005515 Function Protein binding IPI 7904248, 26481812
GO:0005518 Function Collagen binding IDA 10636902, 12972549
GO:0005925 Component Focal adhesion HDA 21423176
GO:0006897 Process Endocytosis IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
612264 16875 ENSG00000011028
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

Accession ID Position in sequence Description Type
PF00040 fn2 187 228 Fibronectin type II domain Domain
PF00059 Lectin_C 255 361 Lectin C-type domain Domain
PF00059 Lectin_C 399 506 Lectin C-type domain Domain
PF00059 Lectin_C 538 646 Lectin C-type domain Domain
PF00059 Lectin_C 693 810 Lectin C-type domain Domain
PF00059 Lectin_C 842 952 Lectin C-type domain Domain
PF00059 Lectin_C 993 1109 Lectin C-type domain Domain
PF00059 Lectin_C 1142 1245 Lectin C-type domain Domain
PF00059 Lectin_C 1285 1395 Lectin C-type domain Domain
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
MGPGRPAPAPWPRHLLRCVLLLGCLHLGRPGAPGDAALPEPNVFLIFSHGLQGCLEAQGG
QVRVTPACNTSLPAQRWKWVSRNRLFNLGTMQCLGTGWPGTNTTASLGMYECDREALNLR
WHCRTLGDQLSLLLGARTSNISKPGTLERGDQTRSGQWRIYGSEEDLCALPYHEVYTIQG
NSHGKPCTIPFKYDNQWFHGCTSTGREDGHLWCATTQDYGKDERWGFCPIKSNDCETFWD
KDQLTDSCYQFNFQSTLSWREAWASCEQQGADLLSITEIHEQTYINGLLTGYSSTLWIGL
NDLDTSGGWQWSDNSPLKYLNWESDQPDNPSEENCGVIRTESSGGWQNRDCSIALPYVCK
K
KPNATAEPTPPDRWANVKVECEPSWQPFQGHCYRLQAEKRSWQESKKACLRGGGDLVSI
HSMAELEFITKQIKQEVEELWIGLNDLKLQMNFEWSDGSLVSFTHWHPFEPNNFRDSLED
CVTIWGPEGRWNDSPCNQSLPSICKK
AGQLSQGAAEEDHGCRKGWTWHSPSCYWLGEDQV
TYSEARRLCTDHGSQLVTITNRFEQAFVSSLIYNWEGEYFWTALQDLNSTGSFFWLSGDE
VMYTHWNRDQPGYSRGGCVALATGSAMGLWEVKNCTSFRARYICRQ
SLGTPVTPELPGPD
PTPSLTGSCPQGWASDTKLRYCYKVFSSERLQDKKSWVQAQGACQELGAQLLSLASYEEE
HFVANMLNKIFGESEPEIHEQHWFWIGLNRRDPRGGQSWRWSDGVGFSYHNFDRSRHDDD
DIRGCAVLDLASLQWVAMQCDTQLDWICKI
PRGTDVREPDDSPQGRREWLRFQEAEYKFF
EHHSTWAQAQRICTWFQAELTSVHSQAELDFLSHNLQKFSRAQEQHWWIGLHTSESDGRF
RWTDGSIINFISWAPGKPRPVGKDKKCVYMTASREDWGDQRCLTALPYICKR
SNVTKETQ
PPDLPTTALGGCPSDWIQFLNKCFQVQGQEPQSRVKWSEAQFSCEQQEAQLVTITNPLEQ
AFITASLPNVTFDLWIGLHASQRDFQWVEQEPLMYANWAPGEPSGPSPAPSGNKPTSCAV
VLHSPSAHFTGRWDDRSCTEETHGFICQK
GTDPSLSPSPAALPPAPGTELSYLNGTFRLL
QKPLRWHDALLLCESRNASLAYVPDPYTQAFLTQAARGLRTPLWIGLAGEEGSRRYSWVS
EEPLNYVGWQDGEPQQPGGCTYVDVDGAWRTTSCDTKLQGAVCGV
SSGPPPPRRISYHGS
CPQGLADSAWIPFREHCYSFHMELLLGHKEARQRCQRAGGAVLSILDEMENVFVWEHLQS
YEGQSRGAWLGMNFNPKGGTLVWQDNTAVNYSNWGPPGLGPSMLSHNSCYWIQSNSGLWR
PGACTNITMGVVCKL
PRAEQSSFSPSALPENPAALVVVLMAVLLLLALLTAALILYRRRQ
SIERGAFEGARYSRSSSSPTEATEKNILVSDMEMNEQQE
Sequence length 1479
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Phagosome
Tuberculosis
  Cross-presentation of soluble exogenous antigens (endosomes)
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Carcinoma Carcinoma, Carcinoma, Spindle-Cell, Undifferentiated carcinoma rs121912654, rs555607708, rs786202962, rs1564055259 16316942
Unknown
Disease term Disease name Evidence References Source
Diabetes Diabetes GWAS
Associations from Text Mining
Disease Name Relationship Type References
Aortic Root Aneurysm Inhibit 33230159
Calcinosis Cutis Associate 26567111
Carcinoma Renal Cell Stimulate 34768883
Glioblastoma Associate 20339555, 28365151
Glioma Associate 20339555
Marfan Syndrome Inhibit 33230159
Mesothelioma Malignant Stimulate 34768883
Neoplasms Associate 20339555, 25162823, 26567111, 37340445
Osteosarcoma Associate 35312779
Ovarian Neoplasms Associate 34336102, 39972314