MSH2 GLN601TER [nucleoplasm]

Stable Identifier
R-HSA-5577243
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
nucleoplasm
Synonyms
MSH2, DNA mismatch repair protein Msh2, MSH2_HUMAN
Icon
MSH2 GLN601TER [nucleoplasm] icon
MSH2 GLN601TER [nucleoplasm] icon
Locations in the PathwayBrowser
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Literature References
PubMed ID Title Journal Year
7713503 Structure of the human MSH2 locus and analysis of two Muir-Torre kindreds for msh2 mutations

Kolodner, RD, Hall, NR, Lipford, J, Kane, MF, Rao, MR, Morrison, P, Wirth, L, Finan, PJ, Burn, J, Chapman, P

Genomics 1994
External Reference Information
External Reference
UniProt:P43246 MSH2
Gene Names
MSH2
Chain
initiator methionine:1, chain:2-934
Reference Genes
BioGPS Gene:4436 MSH2
COSMIC (genes):MSH2 MSH2
CTD Gene:4436 MSH2
dbSNP Gene:4436 MSH2
ENSEMBL:ENSG00000095002 MSH2
HGNC:7325 MSH2
KEGG:hsa:4436 MSH2
Monarch:4436 MSH2
NCBI Entrez Gene:4436 MSH2
OMIM:609309 MSH2
UCSC:P43246 MSH2
Reference Transcript
Other Identifiers
11719416_s_at
11744721_s_at
11749490_x_at
16879883
209421_PM_at
209421_at
2480993
2480994
2480995
2480996
2480997
2480998
2480999
2481000
2481002
2481003
2481007
2481010
2481011
2481016
2481017
2481018
2481020
2481022
2481023
2481025
2481029
2481030
2481031
2481032
2481039
2481042
2481065
2481089
2481091
2481093
2481123
2481124
2481135
2481136
2481137
4436
8041867
860_at
861_g_at
86665_at
A_14_P118153
A_14_P118983
A_23_P102471
A_33_P3287502
A_33_P3287507
GE528310
GE557698
GE58211
GE837848
GO:0000166
GO:0000287
GO:0000400
GO:0000781
GO:0001701
GO:0002204
GO:0002376
GO:0003677
GO:0003682
GO:0003684
GO:0003690
GO:0003697
GO:0003824
GO:0005515
GO:0005524
GO:0005634
GO:0005654
GO:0005694
GO:0006119
GO:0006281
GO:0006298
GO:0006301
GO:0006302
GO:0006310
GO:0006312
GO:0006974
GO:0007281
GO:0008047
GO:0008094
GO:0008340
GO:0008584
GO:0008630
GO:0010165
GO:0010224
GO:0016020
GO:0016446
GO:0016447
GO:0016787
GO:0016887
GO:0019237
GO:0019724
GO:0022414
GO:0030154
GO:0030183
GO:0030983
GO:0031573
GO:0032137
GO:0032139
GO:0032142
GO:0032143
GO:0032181
GO:0032301
GO:0032302
GO:0032357
GO:0032405
GO:0042771
GO:0042803
GO:0043524
GO:0043531
GO:0043570
GO:0045190
GO:0045910
GO:0048298
GO:0048304
GO:0048856
GO:0051726
GO:0098772
GO:0140097
GO:0140657
GO:0140664
HMNXSV003037227
HMNXSV003039134
HMNXSV003050617
ILMN_1737413
ILMN_2203453
PH_hs_0025783
TC02000295.hg
TC02003219.hg
U03911_at
g432997_3p_at
g432997_3p_x_at
Participates
as a member of
Other forms of this molecule
MSH2 [nucleoplasm]
MSH2 R406* [nucleoplasm]
Modified Residues
Name
glycine 601 replaced with unknown
Coordinate
601
PsiMod
glycine removal [MOD:01638]
A protein modification that effectively removes or replaces an glycine.
Cross References
RefSeq
OpenTargets
ENSEMBL
HPA
GeneCards
PRO
Pharos - Targets
Orphanet
GlyGen
PDB
Interactors (19)
Accession #Entities Entities Confidence Score Evidence (IntAct)
 UniProt:P20585 MSH3  2 0.918 14
 UniProt:P52701 MSH6  2 0.91 11
 UniProt:Q9NXL9 MCM9      0.69 9
 UniProt:Q9UQ84-1 EXO1      0.573 3
 UniProt:Q8IY92 SLX4  1 0.567 5
 UniProt:Q92624 APBP2      0.556 3
 UniProt:Q9UJA3 MCM8  1 0.527 3
 UniProt:Q13573 SNW1  1 0.527 2
 UniProt:Q96FW1 OTUB1  2 0.527 3
 UniProt:Q9H4L7 SMRCD      0.527 5
 UniProt:Q5S007 LRRK2  1 0.527 3
 UniProt:P31749 AKT1  14 0.519 2
 UniProt:O60729 CDC14B  1 0.519 2
 UniProt:P04049 RAF1  20 0.508 2
 UniProt:P39875  1 0.508 2
 UniProt:P09429 HMGB1  5 0.499 2
 IntAct:EBI-1187714 41      0.499 2
 UniProt:O00716 E2F3  2 0.483 2
 UniProt:Q9Q2G4 Q9Q2G4      0.462 2
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