MRC1 (mannose receptor C-type 1)
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Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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4360 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Mannose receptor C-type 1 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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MRC1 |
SynonymsGene synonyms aliases
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CD206, CLEC13D, CLEC13DL, MMR, MRC1L1, bA541I19.1, hMR |
ChromosomeChromosome number
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10 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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10p12.33 |
SummarySummary of gene provided in NCBI Entrez Gene.
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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 |
SNPsSNP information provided by dbSNP.
|
SNP ID |
Visualize variation |
Clinical significance |
Consequence |
rs606231248 |
G>A |
Risk-factor |
Coding sequence variant, missense variant |
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miRNAmiRNA 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 IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
|
UniProt ID |
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 |
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Sequence |
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Sequence length |
1456 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Dermatitis |
Dermatitis, Allergic Contact |
rs61816761, rs150597413, rs138726443, rs201356558, rs149484917, rs372754256, rs747301529, rs567795279, rs745915174 |
16033404 |
Hyperinsulinism |
Hyperinsulinism |
rs387906407, rs151344623, rs121913156, rs137853245, rs80356655, rs104894010, rs104894012, rs104894014, rs104894015, rs137852676, rs587783169, rs72559716, rs541269678, rs151344624, rs797045209, rs761749884, rs797045624, rs863225280, rs139964066, rs1057516281, rs1057516317, rs576684889, rs201682634, rs1350717554, rs768951263, rs1260178539, rs200670692, rs72559734, rs1400535021, rs372307320, rs1554923999, rs751279984, rs1008906426, rs367850779, rs1382448285, rs1564977373, rs750586210, rs1599937180 |
29035695 |
Obesity |
Obesity |
rs34911341, rs74315349, rs1474810899, rs2282440, rs2491132, rs121918111, rs796065034, rs753856820, rs796065035, rs121918112, rs104894023, rs137852821, rs1580764441, rs137852822, rs137852823, rs137852824, rs13447324, rs121913562, rs121913564, rs74315393, rs121913556, rs2989924, rs193922650, rs193922685, rs193922687, rs751160202, rs1421085, rs747681609, rs1553400259, rs13447339, rs370479598, rs1554394014, rs1553174844, rs756232889, rs369841551, rs1557670950, rs1571321748, rs148538980, rs1572820988, rs1591461970, rs1419374563, rs745921568, rs144159890, rs1570714352, rs779783209, rs1573250294, rs1573254045, rs1580744791, rs1580746829, rs6548238, rs7138803, rs7754840 |
29035695 |
|
Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Compensatory hyperinsulinemia |
Compensatory Hyperinsulinemia |
|
29035695 |
Endogenous hyperinsulinism |
Endogenous Hyperinsulinism |
|
29035695 |
Exogenous hyperinsulinism |
Exogenous Hyperinsulinism |
|
29035695 |
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