MRC1 (mannose receptor C-type 1)

Gene Gene information from NCBI Gene database.
Gene SNPs miRNA Gene ontology Other IDs Protein Pathways Associated diseases
Entrez ID 4360
Gene name Mannose receptor C-type 1
Gene symbol MRC1
Synonyms (NCBI Gene)
CD206CLEC13DCLEC13DLMMRMRC1L1bA541I19.1hMR
Chromosome 10
Chromosome location 10p12.33
Summary The recognition of complex carbohydrate structures on glycoproteins is an important part of several biological processes, including cell-cell recognition, serum glycoprotein turnover, and neutralization of pathogens. The protein encoded by this gene is a
SNPs SNP information provided by dbSNP.
1
Gene SNPs miRNA Gene ontology Other IDs Protein Pathways Associated diseases
Show/Hide all (1)
SNP ID Visualize variation Clinical significance Consequence
rs606231248 G>A Risk-factor Coding sequence variant, missense variant
miRNA miRNA information provided by mirtarbase database.
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Gene SNPs miRNA Gene ontology Other IDs Protein Pathways Associated diseases
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miRTarBase ID miRNA Experiments Reference
MIRT442609 hsa-miR-4480 PAR-CLIP 22100165
MIRT442608 hsa-miR-4448 PAR-CLIP 22100165
MIRT442609 hsa-miR-4480 PAR-CLIP 22100165
MIRT442608 hsa-miR-4448 PAR-CLIP 22100165
MIRT1157619 hsa-miR-105 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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Gene SNPs miRNA Gene ontology Other IDs Protein Pathways Associated diseases
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GO ID Ontology Definition Evidence Reference
GO:0001618 Function Virus receptor activity IEA
GO:0004888 Function Transmembrane signaling receptor activity IEA
GO:0005515 Function Protein binding IPI 11222859
GO:0005537 Function D-mannose binding IEA
GO:0005537 Function D-mannose binding TAS 2373685
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
Gene SNPs miRNA Gene ontology Other IDs Protein Pathways Associated diseases
MIM HGNC e!Ensembl
153618 7228 ENSG00000260314
Protein Protein information from UniProt database.
Gene SNPs miRNA Gene ontology Other IDs Protein Pathways Associated diseases
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P22897
Protein name Macrophage mannose receptor 1 (MMR) (C-type lectin domain family 13 member D) (C-type lectin domain family 13 member D-like) (Human mannose receptor) (hMR) (Macrophage mannose receptor 1-like protein 1) (CD antigen CD206)
Protein function Mediates the endocytosis of glycoproteins by macrophages. Binds both sulfated and non-sulfated polysaccharide chains.; (Microbial infection) Acts as a phagocytic receptor for bacteria, fungi and other pathogens.; (Microbial i
PDB 1EGG , 1EGI , 5XTS , 5XTW , 6INN , 6INO , 6INU , 6INV , 6IOE , 7JUB , 7JUC , 7JUD , 7JUE , 7JUF , 7JUG , 7JUH , 7L61 , 7L62 , 7L63 , 7L64 , 7L65 , 7L66 , 7L67 , 7L68
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00652 Ricin_B_lectin 23 → 118 Ricin-type beta-trefoil lectin domain Domain
PF00040 fn2 168 → 209 Fibronectin type II domain Domain
PF00059 Lectin_C 236 → 342 Lectin C-type domain Domain
PF00059 Lectin_C 380 → 488 Lectin C-type domain Domain
PF00059 Lectin_C 521 → 627 Lectin C-type domain Domain
PF00059 Lectin_C 669 → 779 Lectin C-type domain Domain
PF00059 Lectin_C 817 → 924 Lectin C-type domain Domain
PF00059 Lectin_C 966 → 1081 Lectin C-type domain Domain
PF00059 Lectin_C 1112 → 1214 Lectin C-type domain Domain
PF00059 Lectin_C 1252 → 1357 Lectin C-type domain Domain
Sequence 
MRLPLLLVFASVIPGAVLLLDTRQFLIYNEDHKRCVDAVSPSAVQTAACNQDAESQKFRW
VSESQIMSVAFKLCLGVPSKTDWVAITLYACDSKSEFQKWECKNDTLLGIKGEDLFFNYG
NRQEKNIMLYKGSGLWSRWKIYGTTDNLCSRGYEAMYTLLGNANGATCAFPFKFENKWYA
DCTSAGRSDGWLWCGTTTDYDTDKLFGYCPLKFEGSESLWNKDPLTSVSYQINSKSALTW
HQARKSCQQQNAELLSITEIHEQTYLTGLTSSLTSGLWIGLNSLSFNSGWQWSDRSPFRY
LNWLPGSPSAEPGKSCVSLNPGKNAKWENLECVQKLGYICKKGNTTLNSFVIPSESDVPT
HCPSQWWPYAGHCYKIHRDEKKIQRDALTTCRKEGGDLTSIHTIEELDFIISQLGYEPND
ELWIGLNDIKIQMYFEWSDGTPVTFTKWLRGEPSHENNRQEDCVVMKGKDGYWADRGCEW
PLGYICKMKSRSQGPEIVEVEKGCRKGWKKHHFYCYMIGHTLSTFAEANQTCNNENAYLT
TIEDRYEQAFLTSFVGLRPEKYFWTGLSDIQTKGTFQWTIEEEVRFTHWNSDMPGRKPGC
VAMRTGIAGGLWDVLKCDEKAKFVCKHWAEGVTHPPKPTTTPEPKCPEDWGASSRTSLCF
KLYAKGKHEKKTWFESRDFCRALGGDLASINNKEEQQTIWRLITASGSYHKLFWLGLTYG
SPSEGFTWSDGSPVSYENWAYGEPNNYQNVEYCGELKGDPTMSWNDINCEHLNNWICQIQ
KGQTPKPEPTPAPQDNPPVTEDGWVIYKDYQYYFSKEKETMDNARAFCKRNFGDLVSIQS
ESEKKFLWKYVNRNDAQSAYFIGLLISLDKKFAWMDGSKVDYVSWATGEPNFANEDENCV
TMYSNSGFWNDINCGYPNAFICQRHNSSINATTVMPTMPSVPSGCKEGWNFYSNKCFKIF
GFMEEERKNWQEARKACIGFGGNLVSIQNEKEQAFLTYHMKDSTFSAWTGLNDVNSEHTF
LWTDGRGVHYTNWGKGYPGGRRSSLSYEDADCVVIIGGASNEAGKWMDDTCDSKRGYICQ
TRSDPSLTNPPATIQTDGFVKYGKSSYSLMRQKFQWHEAETYCKLHNSLIASILDPYSNA
FAWLQMETSNERVWIALNSNLTDNQYTWTDKWRVRYTNWAADEPKLKSACVYLDLDGYWK
TAHCNESFYFLCKRSDEIPATEPPQLPGRCPESDHTAWIPFHGHCYYIESSYTRNWGQAS
LECLRMGSSLVSIESAAESSFLSYRVEPLKSKTNFWIGLFRNVEGTWLWINNSPVSFVNW
NTGDPSGERNDCVALHASSGFWSNIHCSSYKGYICKRPKIIDAKPTHELLTTKADTRKMD
PSKPSSNVAGVVIIVILLILTGAGLAAYFFYKKRRVHLPQEGAFENTLYFNSQSSPGTSD
MKDLVGNIEQNEHSVI
Sequence length 1456
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
Gene SNPs miRNA Gene ontology Other IDs Protein Pathways Associated diseases
  KEGG  Reactome
  Phagosome
Tuberculosis 		  Cross-presentation of soluble exogenous antigens (endosomes)
Modulation by Mtb of host immune system
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
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Gene SNPs miRNA Gene ontology Other IDs Protein Pathways Associated diseases
Show/Hide Unknown Diseases (2)
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Leprosy, susceptibility to, 1 risk factor; Uncertain risk allele rs606231248 RCV002291554
Susceptibility to leprosy and multibacillary leprosy risk factor; Uncertain risk allele rs606231248 RCV000054833
Show/Hide Text Mining Associations (123)
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Adrenoleukodystrophy Associate 29860501
Anemia Iron Deficiency Inhibit 27999815
Anti Neutrophil Cytoplasmic Antibody Associated Vasculitis Associate 36183584
Arthritis Juvenile Associate 21526507, 32787920, 33836809
Arthritis Rheumatoid Associate 39321281
Asthma Associate 33840588
Atherosclerosis Associate 28818858
Autism Spectrum Disorder Associate 32129578
Blast Injuries Inhibit 36508265
Brain Injuries Associate 39191768