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 INMT
Gene summary
Basic gene Info.Gene symbolINMT
Gene nameindolethylamine N-methyltransferase
SynonymsTEMT
CytomapUCSC genome browser: 7p14.3
Type of geneprotein-coding
RefGenesNM_001199219.1,
NM_006774.4,
Descriptionamine N-methyltransferasearomatic alkylamine N-methyltransferasearylamine N-methyltransferaseindolamine N-methyltransferasenicotine N-methyltransferasethioether S-methyltransferase
Modification date20141207
dbXrefs MIM : 604854
HGNC : HGNC
Ensembl : ENSG00000241644
HPRD : 06890
Vega : OTTHUMG00000167163
ProteinUniProt: O95050
go to UniProt's Cross Reference DB Table
ExpressionCleanEX: HS_INMT
BioGPS: 11185
PathwayNCI Pathway Interaction Database: INMT
KEGG: INMT
REACTOME: INMT
Pathway Commons: INMT
ContextiHOP: INMT
ligand binding site mutation search in PubMed: INMT
UCL Cancer Institute: INMT
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:0009308amine metabolic process10552930
GO:0032259methylation10552930


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Ligand binding site mutations for INMT
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
N90R91WCOAD1
L163L161FCOAD1
T67,G65P66LKIRC1
T87T87NLUAD1
Y20D19YLUAD1
D85L83VLUAD1
D85D85ELUSC1
Y25T23ALUSC1
N90R91QPRAD1
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 INMT
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
Y25T23A-1.5343249
T87T87N-1.4375862
D85L83V-0.90624286
D85D85E-0.74880644
T67P66L-0.50877166
G65P66L-0.50877166
N90R91Q-0.50148913
Y20D19Y-0.40381341
L163L161F-0.17626607
N90R91W-0.17241707
(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 INMT from PDB

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Differential gene expression and gene-gene network for INMT
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 INMT and the right PPI network was created from samples without mutations in the LBS of INMT. 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 INMT
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 INMT
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 INMT go to BioLip
Ligand IDLigand short nameLigand long namePDB IDPDB namemutLBS
SAHS-ADENOSYL-L-HOMOCYSTEINE2a14AY20 Y25 G65 T67 D85 T87 N90 L163


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Conservation information for LBS of INMT
Multiple alignments for O95050 in multiple species
LBSAA sequence# speciesSpecies


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