Mus musculus Gene: Pms2
Summary
InnateDB Gene IDBG-259679.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Pms2
Gene Name postmeiotic segregation increased 2 (S. cerevisiae)
Synonyms AW555130; Pmsl2
Species Mus musculus
Ensembl Gene ENSMUSG00000079109
Encoded Proteins
postmeiotic segregation increased 2 (S. cerevisiae)
postmeiotic segregation increased 2 (S. cerevisiae)
postmeiotic segregation increased 2 (S. cerevisiae)
postmeiotic segregation increased 2 (S. cerevisiae)
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000122512:
This gene is one of the PMS2 gene family members found in clusters on chromosome 7. The product of this gene is involved in DNA mismatch repair. It forms a heterodimer with MLH1 and this complex interacts with other complexes bound to mismatched bases. Mutations in this gene are associated with hereditary nonpolyposis colorectal cancer, Turcot syndrome, and are a cause of supratentorial primitive neuroectodermal tumors. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 5:143909964-143937309
Strand Forward strand
Band G2
Transcripts
ENSMUST00000110710
ENSMUST00000110709 ENSMUSP00000106337
ENSMUST00000110707
ENSMUST00000148011 ENSMUSP00000119875
ENSMUST00000141942
ENSMUST00000147910
ENSMUST00000126331
ENSMUST00000154781
ENSMUST00000128153
ENSMUST00000128207
ENSMUST00000170083
ENSMUST00000168085
ENSMUST00000164999 ENSMUSP00000133062
ENSMUST00000172367 ENSMUSP00000132104
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 43 interaction(s) predicted by orthology.
Predicted by orthology
Total 43 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003677 DNA binding
GO:0003697 single-stranded DNA binding
GO:0005515 protein binding
GO:0005524 ATP binding
GO:0016887 ATPase activity
GO:0030983 mismatched DNA binding
GO:0032138 single base insertion or deletion binding
GO:0032407 MutSalpha complex binding
Biological Process
GO:0006200 ATP catabolic process
GO:0006281 DNA repair
GO:0006298 mismatch repair
GO:0006974 cellular response to DNA damage stimulus
GO:0007126 meiotic nuclear division
GO:0016446 somatic hypermutation of immunoglobulin genes
GO:0016447 somatic recombination of immunoglobulin gene segments
GO:0042493 response to drug
Cellular Component
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0015630 microtubule cytoskeleton
GO:0032389 MutLalpha complex
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
KEGG
Mismatch repair pathway
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha) pathway
Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta) pathway
Mismatch Repair pathway
DNA Repair pathway
KEGG
Mismatch repair pathway
INOH
PID NCI
Direct p53 effectors
Cross-References
SwissProt
TrEMBL A4QPD7 E9QLM4
UniProt Splice Variant
Entrez Gene 18861
UniGene Mm.2950 Mm.398563
RefSeq NM_008886 XM_006504812 XM_006504813 XM_006504814
OMIM
CCDS CCDS39375
HPRD
IMGT
MGI ID MGI:104288
MGI Symbol Pms2
EMBL AC121917 BC139774
GenPept AAI39775
RNA Seq Atlas 18861