mutLBSgeneDB |
Gene summary for CLEC4M |
Gene summary |
Basic gene Info. | Gene symbol | CLEC4M |
Gene name | C-type lectin domain family 4, member M | |
Synonyms | CD209L|CD299|DC-SIGN2|DC-SIGNR|DCSIGNR|HP10347|L-SIGN|LSIGN | |
Cytomap | UCSC genome browser: 19p13 | |
Type of gene | protein-coding | |
RefGenes | NM_001144904.1, NM_001144905.1,NM_001144906.1,NM_001144907.1,NM_001144908.1, NM_001144909.1,NM_001144910.1,NM_001144911.1,NM_014257.4, NR_026707.1,NR_026708.1,NR_026709.1,NM_214675.1, NM_214676.1, | |
Description | C-type lectin domain family 4 member MCD209 antigen-like protein 1CD299 antigenDC-SIGN-related proteindendritic cell-specific ICAM-3-grabbing non-integrin 2liver/lymph node-specific ICAM-3 grabbing non-integrinliver/lymph node-specific ICAM-3-grabbi | |
Modification date | 20141207 | |
dbXrefs | MIM : 605872 | |
HGNC : HGNC | ||
Ensembl : ENSG00000104938 | ||
HPRD : 12060 | ||
Vega : OTTHUMG00000182432 | ||
Protein | UniProt: Q9H2X3 go to UniProt's Cross Reference DB Table | |
Expression | CleanEX: HS_CLEC4M | |
BioGPS: 10332 | ||
Pathway | NCI Pathway Interaction Database: CLEC4M | |
KEGG: CLEC4M | ||
REACTOME: CLEC4M | ||
Pathway Commons: CLEC4M | ||
Context | iHOP: CLEC4M | |
ligand binding site mutation search in PubMed: CLEC4M | ||
UCL Cancer Institute: CLEC4M | ||
Assigned class in mutLBSgeneDB | C: This gene just belongs to mutLBSgenes. |
Gene ontology having evidence of Inferred from Direct Assay (IDA) from Entrez |
GO ID | GO Term | PubMed ID |
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Ligand binding site mutations for CLEC4M |
Cancer type specific mutLBS sorted by frequency |
LBS | AAchange of nsSNV | Cancer type | # samples | E359 | E359D | SKCM | 1 | D256 | D256N | UCEC | 1 | D367 | A369V | UCEC | 1 | D332 | D332Y | UCEC | 1 |
cf) Cancer type abbreviation. BLCA: Bladder urothelial carcinoma, BRCA: Breast invasive carcinoma, CESC: Cervical squamous cell carcinoma and endocervical adenocarcinoma, COAD: Colon adenocarcinoma, GBM: Glioblastoma multiforme, LGG: Brain lower grade glioma, HNSC: Head and neck squamous cell carcinoma, KICH: Kidney chromophobe, KIRC: Kidney renal clear cell carcinoma, KIRP: Kidney renal papillary cell carcinoma, LAML: Acute myeloid leukemia, LUAD: Lung adenocarcinoma, LUSC: Lung squamous cell carcinoma, OV: Ovarian serous cystadenocarcinoma, PAAD: Pancreatic adenocarcinoma, PRAD: Prostate adenocarcinoma, SKCM: Skin cutaneous melanoma, STAD: Stomach adenocarcinoma, THCA: Thyroid carcinoma, UCEC: Uterine corpus endometrial carcinoma. |
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Protein structure related information for CLEC4M |
Relative protein structure stability change (ΔΔE) using Mupro 1.1 Mupro score denotes assessment of the effect of mutations on thermodynamic stability. (ΔΔE<0: mutation decreases stability, ΔΔE>0: mutation increases stability) |
: nsSNV at non-LBS: nsSNV at LBS |
nsSNVs sorted by the relative stability change of protein structure by each mutation Blue: mutations of positive stability change. and red : the most recurrent mutation for this gene. |
LBS | AAchange of nsSNV | Relative stability change | E359 | E359D | -1.6213935 | D256 | D256N | -1.0923206 | D367 | A369V | -0.53195712 | D332 | D332Y | -0.14237677 |
(MuPro1.1: Jianlin Cheng et al., Prediction of Protein Stability Changes for Single-Site Mutations Using Support Vector Machines, PROTEINS: Structure, Function, and Bioinformatics. 2006, 62:1125-1132) |
Structure image for CLEC4M from PDB |
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Differential gene expression and gene-gene network for CLEC4M |
Differential gene expression between mutated and non-mutated LBS samples in all 16 major cancer types |
Differential co-expressed gene network based on protein-protein interaction data (CePIN) |
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Phenotype information for CLEC4M |
Gene level disease information (DisGeNet) |
Disease ID | Disease name | # PubMed | Association type |
Mutation level pathogenic information (ClinVar annotation) |
Allele ID | AA change | Clinical significance | Origin | Phenotype IDs |
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Pharmacological information for CLEC4M |
Gene expression profile of anticancer drug treated cell-lines (CCLE) Heatmap showing the correlation between gene expression and drug response across all the cell-lines. We chose the top 20 among 138 drugs.We used Pearson's correlation coefficient. |
Drug information targeting mutLBSgene (Approved drugs only) |
Drug status | DrugBank ID | Name | Type | Drug structure |
Gene-centered ligand-gene interaction network |
Ligands binding to mutated ligand binding site of CLEC4M go to BioLip |
Ligand ID | Ligand short name | Ligand long name | PDB ID | PDB name | mutLBS | CA | CALCIUM(2+) | 1sl6 | A | D256 | CA | CALCIUM(2+) | 1sl6 | B | D256 | CA | CALCIUM(2+) | 1sl6 | C | D256 | CA | CALCIUM(2+) | 1sl6 | D | D256 | CA | CALCIUM(2+) | 1k9j | A | D332 D367 | CA | CALCIUM(2+) | 1sl6 | A | D332 D367 | CA | CALCIUM(2+) | 1sl6 | B | D332 D367 | CA | CALCIUM(2+) | 1sl6 | C | D332 D367 | CA | CALCIUM(2+) | 1sl6 | D | D332 D367 | CA | CALCIUM(2+) | 1sl6 | E | D332 D367 | CA | CALCIUM(2+) | 1sl6 | F | D332 D367 | CA | CALCIUM(2+) | 1k9j | A | D367 | CA | CALCIUM(2+) | 1sl6 | A | D367 | CA | CALCIUM(2+) | 1sl6 | B | D367 | CA | CALCIUM(2+) | 1sl6 | C | D367 | CA | CALCIUM(2+) | 1sl6 | D | D367 | CA | CALCIUM(2+) | 1sl6 | E | D367 | CA | CALCIUM(2+) | 1sl6 | F | D367 | MAN | ALPHA-D-MANNOSE | 1k9j | A | E359 | CA | CALCIUM(2+) | 1k9j | A | E359 | FUC | ALPHA-L-FUCOPYRANOSE | 1sl6 | A | E359 | CA | CALCIUM(2+) | 1sl6 | A | E359 | FUC | ALPHA-L-FUCOPYRANOSE | 1sl6 | B | E359 | CA | CALCIUM(2+) | 1sl6 | B | E359 | FUC | ALPHA-L-FUCOPYRANOSE | 1sl6 | C | E359 | CA | CALCIUM(2+) | 1sl6 | C | E359 | FUC | ALPHA-L-FUCOPYRANOSE | 1sl6 | D | E359 | CA | CALCIUM(2+) | 1sl6 | D | E359 | FUC | ALPHA-L-FUCOPYRANOSE | 1sl6 | E | E359 | CA | CALCIUM(2+) | 1sl6 | E | E359 | FUC | ALPHA-L-FUCOPYRANOSE | 1sl6 | F | E359 | CA | CALCIUM(2+) | 1sl6 | F | E359 | CA | CALCIUM(2+) | 1xph | A | E359 |
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Conservation information for LBS of CLEC4M |
Multiple alignments for Q9H2X3 in multiple species |
LBS | AA sequence | # species | Species |
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