Gene Report

Basic Information

Approved Symbol	MSH3
Approved Name	mutS homolog 3 (E. coli)
Previous Name	mutS (E. coli) homolog 3
Symbol Alias	DUP, MRP1
Name Alias	Divergent upstream protein, "Mismatch repair protein 1"
Location	5q11-q12
Position	chr5:79950467-80172634 (+)
External Links	Entrez Gene: 4437 Ensembl: ENSG00000113318 UCSC: uc003kgz.3 HGNC ID: 7326
No. of Studies (Positive/Negative)	1(1/0)
Type	Literature-origin

Positive relationships between MSH3 and MDD (count: 1)

Name in Literature	Reference	Research Type	Statistical Result	Relation Description
mutS homolog 3	Tochigi, 2008	patients and normal controls		Genes differentially expressed in major depression Genes differentially expressed in major depression

Positive relationships between MSH3 and other components at different levels (count: 0)

Positive relationship network of MSH3 in MK4MDD

Network loading ...

Note:
1. The different color of the nodes denotes the level of the nodes.

Genetic/Epigenetic Locus	Protein and Other Molecule	Cell and Molecular Pathway	Neural System	Cognition and Behavior	Symptoms and Signs	Environment	MDD

2. Besides the component related relationships from literature, gene mapped protein and protein mapped gene are also shown in the network. If the mapped gene or protein is not from literature, square node would be used instead of Circle node. Accordingly, the relationship is marked with dot line.
2. User can drag the nodes to rearrange the layout of the network. Click the node will enter the report page of the node. Right-click will show also the menus to link to the report page of the node and remove the node and related edges. Hover the node will show the level of the node and hover the edge will show the evidence/description of the edge.
3. The network is generated using Cytoscape Web

Negative relationships between MSH3 and MDD (count: 0)

Negative relationships between MSH3 and other components at different levels (count: 0)

MSH3 related SNPs in MK4MDD (count: 0)

MSH3 related proteins in MK4MDD (count: 1)

Approved Name	UniportKB	No. of Studies (Positive/Negative)	Source
DNA mismatch repair protein Msh3	P20585	0(0/0)	Gene mapped

MSH3 related GO terms (count: 29)

ID	Name	Type	Evidence
Literature-origin GO terms
GO:0032553	ribonucleotide binding	molecular function	IEA
GO:0032553	ribonucleotide binding	molecular function	IEA

ID	Name	Type	Evidence
Gene mapped GO terms
GO:0000403	Y-form DNA binding	molecular function	IBA
GO:0043570	maintenance of DNA repeat elements	biological process	IMP[16388310]
GO:0005634	nucleus	cellular component	IDA
GO:0032181	dinucleotide repeat insertion binding	molecular function	IDA[8942985]
GO:0042803	protein homodimerization activity	molecular function	IDA[8942985]
GO:0019237	centromeric DNA binding	molecular function	IEA
GO:0000228	nuclear chromosome	cellular component	IBA
GO:0006298	mismatch repair	biological process	IMP[8782829]
GO:0005515	protein binding	molecular function	IPI[9774676]
GO:0006281	DNA repair	biological process	IDA[8942985]
GO:0032137	guanine/thymine mispair binding	molecular function	IDA[11809883]
GO:0032139	dinucleotide insertion or deletion binding	molecular function	IDA[8942985]
GO:0051096	positive regulation of helicase activity	biological process	IDA[17715146]
GO:0016447	somatic recombination of immunoglobulin gene segments	biological process	IBA
GO:0030983	mismatched DNA binding	molecular function	IDA[8942985]
GO:0045910	negative regulation of DNA recombination	biological process	IDA[17715146]
GO:0007131	reciprocal meiotic recombination	biological process	IBA
GO:0005524	ATP binding	molecular function	IEA
GO:0032357	oxidized purine DNA binding	molecular function	IDA[11756455]
GO:0032142	single guanine insertion binding	molecular function	IDA[8942985]
GO:0032302	MutSbeta complex	cellular component	IDA[8942985]
GO:0000710	meiotic mismatch repair	biological process	IBA
GO:0000404	loop DNA binding	molecular function	IBA
GO:0008094	DNA-dependent ATPase activity	molecular function	IBA
GO:0000406	double-strand/single-strand DNA junction binding	molecular function	IBA
GO:0003697	single-stranded DNA binding	molecular function	IDA[11809883]
GO:0019899	enzyme binding	molecular function	IPI[11427529]

MSH3 related KEGG pathways (count: 3)

ID	Name	Brief Description	Full Description
Gene mapped KEGG pathways
hsa05210	colorectal cancer	Colorectal cancer	Classically, colorectal cancer (CRC) has been believed to de...... Classically, colorectal cancer (CRC) has been believed to develop from normal mucosa through the premalignant adenoma by the step-wise accumulation of mutations. All CRC display either microsatellite instability (MSI) or chromosome instability (CIN). MSI occurs in 15% of colon cancers and results from inactivation of the DNA mismatch repair (MMR) system by either MMR gene mutations or hypermethylation of the MLH1 promoter. MSI promotes tumorigenesis through generating mutations in target genes that possess coding microsatellite repeats, such as beta-catenin, TGFBR2 and BAX. CIN is found in the majority of colon cancers and leads to a different pattern of gene alterations that contribute to tumor formation. Genes involved in CIN are those coding for APC, K-ras, SMAD4 and p53. More...
hsa03430	mismatch repair	Mismatch repair	DNA mismatch repair (MMR) is a highly conserved biological p...... DNA mismatch repair (MMR) is a highly conserved biological pathway that plays a key role in maintaining genomic stability. MMR corrects DNA mismatches generated during DNA replication, thereby preventing mutations from becoming permanent in dividing cells. MMR also suppresses homologous recombination and was recently shown to play a role in DNA damage signaling. Defects in MMR are associated with genome-wide instability, predisposition to certain types of cancer including HNPCC, resistance to certain chemotherapeutic agents, and abnormalities in meiosis and sterility in mammalian systems. The Escherichia coli MMR pathway has been extensively studied and is well characterized. In E. coli, the mismatch-activated MutS-MutL-ATP complex licenses MutH to incise the nearest unmethylated GATC sequence. UvrD and an exonuclease generate a gap. This gap is filled by pol III and DNA ligase. The GATC sites are then methylated by Dam. Several human MMR proteins have been identified based on their homology to E. coli MMR proteins. These include human homologs of MutS and MutL. Although E. coli MutS and MutL proteins are homodimers, human MutS and MutL homologs are heterodimers. The role of hemimethylated dGATC sites as a signal for strand discrimination is not conserved from E. coli to human. Human MMR is presumed to be nick-directed in vivo, and is thought to discriminate daughter and template strands using a strand-specific nick. More...
hsa05200	pathways in_cancer	Pathways in cancer

MSH3 related BioCarta pathways (count: 0)

MSH3 related Reactome pathways (count: 0)

MSH3 related interactors from protein-protein interaction data in HPRD (count: 3)

Gene	Interactor	Interactor in MK4MDD?	Experiment Type	PMID
MSH3	EXO1	No	in vitro;in vivo	11427529
MSH3	MSH2	Yes	in vitro;in vivo;yeast 2-hybrid	9774676 , 8942985
MSH3	PCNA	No	in vitro;in vivo	11274057 , 11005803 , 12171929

Gene Report

Literature-origin GO terms

Gene mapped GO terms

Gene mapped KEGG pathways