mutLBSgeneDB

mutLBSgeneDB
mutated Ligand Binding Site gene DataBase

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Gene Summary

Ligand Binding Site Mutation Information

Protein Structure Related Information

Gene Expression and Gene-Gene Network

Phenotype Information

Pharmacological Information

Conservation Information for LBS

Gene summary for CXXC1
Gene summary
Basic gene Info.Gene symbolCXXC1
Gene nameCXXC finger protein 1
Synonyms2410002I16Rik|5830420C16Rik|CFP1|CGBP|HsT2645|PCCX1|PHF18|SPP1|ZCGPC1|hCGBP
CytomapUCSC genome browser: 18q12
Type of geneprotein-coding
RefGenesNM_001101654.1,
NM_014593.3,
DescriptionCXXC finger 1 (PHD domain)CXXC-type zinc finger protein 1CpG binding proteinDNA-binding protein with PHD finger and CXXC domainPHD finger and CXXC domain-containing protein 1cpG-binding proteinzinc finger, CpG binding-type containing 1
Modification date20141207
dbXrefs MIM : 609150
HGNC : HGNC
Ensembl : ENSG00000154832
HPRD : 10852
Vega : OTTHUMG00000132670
ProteinUniProt: Q9P0U4
go to UniProt's Cross Reference DB Table
ExpressionCleanEX: HS_CXXC1
BioGPS: 30827
PathwayNCI Pathway Interaction Database: CXXC1
KEGG: CXXC1
REACTOME: CXXC1
Pathway Commons: CXXC1
ContextiHOP: CXXC1
ligand binding site mutation search in PubMed: CXXC1
UCL Cancer Institute: CXXC1
Assigned class in mutLBSgeneDBC: This gene just belongs to mutLBSgenes.

Gene ontology having evidence of Inferred from Direct Assay (IDA) from Entrez
GO IDGO TermPubMed ID
GO:0006355regulation of transcription, DNA-templated10688657
GO:0045893positive regulation of transcription, DNA-templated10688657
GO:0051568histone H3-K4 methylation17355966


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Ligand binding site mutations for CXXC1
Lollipop-style diagram of mutations at LBS in amino-acid sequence.
We represented ligand binding site mutations only. (You can see big image via clicking.)
 
: non-synonymous mutation on LBS, Circle size denotes number of samples.

Cancer type specific mutLBS sorted by frequency
LBSAAchange of nsSNVCancer type# samples
A166S165TSTAD1
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 CXXC1
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.
LBSAAchange of nsSNVRelative stability change
A166S165T-0.15479874
(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 CXXC1 from PDB

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Differential gene expression and gene-gene network for CXXC1
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)
* Left PPI network was created from samples with mutations in the LBS of CXXC1 and the right PPI network was created from samples without mutations in the LBS of CXXC1. Only genes with p-value < 0.05 are shown.
Red circle: input gene. Orange circle: LBSgene. Blue circle: other gene.


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Phenotype information for CXXC1
Gene level disease information (DisGeNet)
Disease IDDisease name# PubMedAssociation type

Mutation level pathogenic information (ClinVar annotation)
Allele IDAA changeClinical significanceOriginPhenotype IDs

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Pharmacological information for CXXC1
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 statusDrugBank IDNameTypeDrug structure

Gene-centered ligand-gene interaction network

Ligands binding to mutated ligand binding site of CXXC1 go to BioLip
Ligand IDLigand short nameLigand long namePDB IDPDB namemutLBS


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Conservation information for LBS of CXXC1
Multiple alignments for Q9P0U4 in multiple species
LBSAA sequence# speciesSpecies
A166QIKRSARMCGE3Homo sapiens, Mus musculus, Bos taurus
C169RSARMCGECEA3Homo sapiens, Mus musculus, Bos taurus
C172RMCGECEACRR3Homo sapiens, Mus musculus, Bos taurus
C175GECEACRRTED3Homo sapiens, Mus musculus, Bos taurus
C208CRLRQCQLRAR3Homo sapiens, Mus musculus, Bos taurus
I199GGPNKIRQKCR3Homo sapiens, Mus musculus, Bos taurus
K198FGGPNKIRQKC3Homo sapiens, Mus musculus, Bos taurus
K202NKIRQKCRLRQ3Homo sapiens, Mus musculus, Bos taurus
Q201PNKIRQKCRLR3Homo sapiens, Mus musculus, Bos taurus
R167IKRSARMCGEC3Homo sapiens, Mus musculus, Bos taurus
R200GPNKIRQKCRL3Homo sapiens, Mus musculus, Bos taurus
R206QKCRLRQCQLR3Homo sapiens, Mus musculus, Bos taurus
R213CQLRARESYKY3Homo sapiens, Mus musculus, Bos taurus
S215LRARESYKYFP3Homo sapiens, Mus musculus, Bos taurus
Y216RARESYKYFPS3Homo sapiens, Mus musculus, Bos taurus


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