mutLBSgeneDB

mutLBSgeneDB
mutated Ligand Binding Site gene DataBase

Home

Download

 Statistics

Help

About Us

Bioinformatics and Systems Medicine Laboratory Bioinformatics and Systems Medicine Laboratory

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 PDCD10
Gene summary
Basic gene Info.Gene symbolPDCD10
Gene nameprogrammed cell death 10
SynonymsCCM3|TFAR15
CytomapUCSC genome browser: 3q26.1
Type of geneprotein-coding
RefGenesNM_007217.3,
NM_145859.1,NM_145860.1,
DescriptionTF-1 cell apoptosis-related protein 15apoptosis-related protein 15cerebral cavernous malformations 3 proteinprogrammed cell death protein 10
Modification date20141219
dbXrefs MIM : 609118
HGNC : HGNC
Ensembl : ENSG00000114209
HPRD : 10141
Vega : OTTHUMG00000158415
ProteinUniProt: Q9BUL8
go to UniProt's Cross Reference DB Table
ExpressionCleanEX: HS_PDCD10
BioGPS: 11235
PathwayNCI Pathway Interaction Database: PDCD10
KEGG: PDCD10
REACTOME: PDCD10
Pathway Commons: PDCD10
ContextiHOP: PDCD10
ligand binding site mutation search in PubMed: PDCD10
UCL Cancer Institute: PDCD10
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:0008284positive regulation of cell proliferation17360971
GO:0030335positive regulation of cell migration23541896
GO:0032874positive regulation of stress-activated MAPK cascade22652780
GO:0042542response to hydrogen peroxide22291017
GO:0043066negative regulation of apoptotic process17360971
GO:0043406positive regulation of MAP kinase activity17360971


Top
Ligand binding site mutations for PDCD10

Cancer type specific mutLBS sorted by frequency
LBSAAchange of nsSNVCancer type# samples
K70K69NSTAD1
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.


Top
Protein structure related information for PDCD10
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
K70K69N-1.156551
(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 PDCD10 from PDB

Top
Differential gene expression and gene-gene network for PDCD10
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 PDCD10 and the right PPI network was created from samples without mutations in the LBS of PDCD10. Only genes with p-value < 0.05 are shown.
Red circle: input gene. Orange circle: LBSgene. Blue circle: other gene.


Top

Top
Phenotype information for PDCD10
Gene level disease information (DisGeNet)
Disease IDDisease name# PubMedAssociation type

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

Top
Pharmacological information for PDCD10
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 PDCD10 go to BioLip
Ligand IDLigand short nameLigand long namePDB IDPDB namemutLBS
4IPINOSITOL 1,3,4,5-TETRAKISPHOSPHATE3ajmAK70
4IPINOSITOL 1,3,4,5-TETRAKISPHOSPHATE3ajmBK70


Top
Conservation information for LBS of PDCD10
Multiple alignments for Q9BUL8 in multiple species
LBSAA sequence# speciesSpecies
A135TIKDIASAIKE6Homo sapiens, Danio rerio, Xenopus tropicalis, Rattus norvegicus, Gallus gallus, Mus musculus
A135TIKLIASSIKK1Caenorhabditis elegans
F182TLKTYFKDGKA6Homo sapiens, Danio rerio, Xenopus tropicalis, Rattus norvegicus, Gallus gallus, Mus musculus
F182TLKTYFKDQNA1Caenorhabditis elegans
G185TYFKDGKAINV5Homo sapiens, Danio rerio, Rattus norvegicus, Gallus gallus, Mus musculus
G185TYFKDQNANQV1Caenorhabditis elegans
G185TYFKDGKALNV1Xenopus tropicalis
I131RFLQTIKDIAS6Homo sapiens, Danio rerio, Xenopus tropicalis, Rattus norvegicus, Gallus gallus, Mus musculus
I131AFLETIKLIAS1Caenorhabditis elegans
I138DIASAIKELLD6Homo sapiens, Danio rerio, Xenopus tropicalis, Rattus norvegicus, Gallus gallus, Mus musculus
I138LIASSIKKLLE1Caenorhabditis elegans
K132FLQTIKDIASA6Homo sapiens, Danio rerio, Xenopus tropicalis, Rattus norvegicus, Gallus gallus, Mus musculus
K132FLETIKLIASS1Caenorhabditis elegans
K139IASAIKELLDT6Homo sapiens, Danio rerio, Xenopus tropicalis, Rattus norvegicus, Gallus gallus, Mus musculus
K139IASSIKKLLEA1Caenorhabditis elegans
K164ALEHQKKEFVK6Homo sapiens, Danio rerio, Xenopus tropicalis, Rattus norvegicus, Gallus gallus, Mus musculus
K164AVEKRKREFVH1Caenorhabditis elegans
K172FVKYSKSFSDT5Homo sapiens, Xenopus tropicalis, Rattus norvegicus, Gallus gallus, Mus musculus
K172FVHYSKRFSNT1Caenorhabditis elegans
K172FVKHSKSFSDT1Danio rerio
K179FSDTLKTYFKD6Homo sapiens, Danio rerio, Xenopus tropicalis, Rattus norvegicus, Gallus gallus, Mus musculus
K179FSNTLKTYFKD1Caenorhabditis elegans
K186YFKDGKAINVF5Homo sapiens, Danio rerio, Rattus norvegicus, Gallus gallus, Mus musculus
K186YFKDQNANQVS1Caenorhabditis elegans
K186YFKDGKALNVF1Xenopus tropicalis
K70KILEKKSVEVN4Homo sapiens, Xenopus tropicalis, Rattus norvegicus, Mus musculus
K70VLLDDSELSVN1Caenorhabditis elegans
K70KILEKKNVEIN1Danio rerio
K70KILEKKSVDVN1Gallus gallus
L128DRVRFLQTIKD6Homo sapiens, Danio rerio, Xenopus tropicalis, Rattus norvegicus, Gallus gallus, Mus musculus
L128DRHAFLETIKL1Caenorhabditis elegans
L142AIKELLDTVNN6Homo sapiens, Danio rerio, Xenopus tropicalis, Rattus norvegicus, Gallus gallus, Mus musculus
L142SIKKLLEAINA1Caenorhabditis elegans
N146LLDTVNNVFKK6Homo sapiens, Danio rerio, Xenopus tropicalis, Rattus norvegicus, Gallus gallus, Mus musculus
N146LLEAINAVYRI1Caenorhabditis elegans
S171EFVKYSKSFSD5Homo sapiens, Xenopus tropicalis, Rattus norvegicus, Gallus gallus, Mus musculus
S171EFVHYSKRFSN1Caenorhabditis elegans
S171EFVKHSKSFSD1Danio rerio
S175YSKSFSDTLKT5Homo sapiens, Xenopus tropicalis, Rattus norvegicus, Gallus gallus, Mus musculus
S175YSKRFSNTLKT1Caenorhabditis elegans
S175HSKSFSDTLKT1Danio rerio
V168QKKEFVKYSKS5Homo sapiens, Xenopus tropicalis, Rattus norvegicus, Gallus gallus, Mus musculus
V168RKREFVHYSKR1Caenorhabditis elegans
V168QKKEFVKHSKS1Danio rerio


Copyright © 2016-Present - The University of Texas Health Science Center at Houston
Site Policies | State of Texas