Protein Msh2

URN urn:agi-llid:4436
Total Entities 0
Connectivity 442
Name Msh2
Description mutS homolog 2, colon cancer, nonpolyposis type 1 (E. coli)
Notes MSH2 was identified as a locus frequently mutated in hereditary nonpolyposis colon cancer (HNPCC). When cloned, it was discovered to be a human homolog of the E. coli mismatch repair gene mutS, consistent with the characteristic alterations in microsatellite sequences (RER+ phenotype) found in HNPCC.

Ariadne Ontology DNA repair
Biofluids assayable substances

GO Molecular Function protein C-terminus binding
enzyme binding
MutLalpha complex binding
protein kinase binding
protein homodimerization activity
nucleotide binding
ADP binding
ATP binding
DNA binding
damaged DNA binding
centromeric DNA binding
double-stranded DNA binding
single-stranded DNA binding
Y-form DNA binding
loop DNA binding
double-strand-single-strand DNA junction binding
four-way junction DNA binding
mismatched DNA binding
guanine-thymine mispair binding
dinucleotide insertion or deletion binding
single base insertion or deletion binding
single guanine insertion binding
single thymine insertion binding
dinucleotide repeat insertion binding
oxidized purine DNA binding
magnesium ion binding
ATPase activity
DNA-dependent ATPase activity

GO Cellular Component nuclear chromosome
MutSalpha complex
MutSbeta complex
nucleus

GO Biological Process cell cycle
meiotic gene conversion
cell cycle arrest
meiotic mismatch repair
intra-S DNA damage checkpoint
negative regulation of reciprocal meiotic recombination
germ cell development
intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator
negative regulation of DNA recombination
negative regulation of apoptotic process
negative regulation of neuron apoptotic process
B cell differentiation
isotype switching
ATP catabolic process
DNA repair
maintenance of DNA repeat elements
double-strand break repair
postreplication repair
mismatch repair
somatic recombination of immunoglobulin gene segments
somatic recombination of immunoglobulin genes involved in immune response
oxidative phosphorylation
response to DNA damage stimulus
apoptotic process
B cell mediated immunity
somatic hypermutation of immunoglobulin genes
response to drug
response to amino acid stimulus
response to organic cyclic compound
response to UV-B
response to X-ray
positive regulation of helicase activity
male gonad development
in utero embryonic development
determination of adult lifespan
spermatogenesis

Pathway Single-Strand Mismatch DNA Repair
colorectal cancer pathway
colorectal cancer pathway

Group DNA repair
cell cycle
meiotic gene conversion
cell cycle arrest
meiotic mismatch repair
intra-S DNA damage checkpoint
negative regulation of reciprocal meiotic recombination
germ cell development
intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator
negative regulation of DNA recombination
negative regulation of apoptotic process
negative regulation of neuron apoptotic process
B cell differentiation
isotype switching
ATP catabolic process
DNA repair
maintenance of DNA repeat elements
double-strand break repair
postreplication repair
mismatch repair
somatic recombination of immunoglobulin gene segments
somatic recombination of immunoglobulin genes involved in immune response
oxidative phosphorylation
response to DNA damage stimulus
apoptotic process
B cell mediated immunity
somatic hypermutation of immunoglobulin genes
response to drug
response to amino acid stimulus
response to organic cyclic compound
response to UV-B
response to X-ray
positive regulation of helicase activity
male gonad development
in utero embryonic development
determination of adult lifespan
spermatogenesis
protein C-terminus binding
enzyme binding
MutLalpha complex binding
protein kinase binding
protein homodimerization activity
nucleotide binding
ADP binding
ATP binding
DNA binding
damaged DNA binding
centromeric DNA binding
double-stranded DNA binding
single-stranded DNA binding
Y-form DNA binding
loop DNA binding
double-strand-single-strand DNA junction binding
four-way junction DNA binding
mismatched DNA binding
guanine-thymine mispair binding
dinucleotide insertion or deletion binding
single base insertion or deletion binding
single guanine insertion binding
single thymine insertion binding
dinucleotide repeat insertion binding
oxidized purine DNA binding
magnesium ion binding
ATPase activity
DNA-dependent ATPase activity
nuclear chromosome
MutSalpha complex
MutSbeta complex
nucleus
Biofluids assayable substances

MedScan ID 4436

Hugo ID 7325

Human chromosome position 2p21
2p22-p21

GenBank ID NC_000002
NM_000251
NP_000242
NM_001258281
NP_001245210
NG_007110
NC_018913
AC_000134
AC079775
AAY15096
AC138655
AF066081
AAC27930
AY344477
AAQ23475
AY601851
AAS99351
CH471053
EAX00213
EAX00214
EAX00215
U41221
AAA82080
AK222860
BAD96580
AK223284
BAD97004
AK296831
BAG59401
AK297763
BAG60111
AK299667
BAG61581
AK304496
BAG65304
AK311330
BC001122
BC012599
BC021566
AAH21566
BX649122
CB250419
DC342099
DQ648894
ABG49489
DQ648895
ABG49490
DQ648896
ABG49491
DQ648897
ABG49492
L47574
AAB59566
L47575
AAB59567
L47576
AAB59568
L47577
AAB59569
L47578
AAB59570
L47579
AAB59571
L47580
AAB59572
L47581
AAA76858
L47582
AAB59565
L47583
AAB59564
U03911
AAA18643
U04045
AAA61870
P43246
DQ892558
ABM83484
DQ895772
ABM86698
NC_000083
NM_008628
NP_032654
AC_000039
AC163652
CH466537
EDL38635
AK051960
AK078775
AK157842
BAE34223
AK166179
AK206893
AK216255
AK217675
BC047117
AAH47117
BC050897
AAH50897
U21011
AAA75027
X81143
CAA57049
P43247
NC_005105
NM_031058
NP_112320
AC_000074
CH473947
EDM02635
BC161846
AAI61846
X93591
CAA63789
P54275
NT_022184
NW_927719
NW_001838769
AC_000045
Q0ZAI9
Q0ZAJ0
Q0ZAJ1
Q0ZAJ2
Q53FK0
Q53GS1
Q53RU4
Q6VBB7
NT_039649
NW_001030622
Q3TZI5
Q80V79
NW_001084845
NW_047755

LocusLink ID 4436
17685
81709

Alias FCC1
COCA1
HNPCC
LCFS2
HNPCC1
DNA mismatch repair protein Msh2
hMSH2
AI788990
mutS protein homolog 2
mismatch repair protein
OTTHUMP00000200306
Msh2
Lynch cancer family syndrome II gene
Lynch cancer family syndrome II protein
mismatch repair protein 2
mismatch repair protein II
mutS (E. coli) homolog 2
mutS (E. coli) homolog II
mutS homolog 2
mutS homolog 2 (E. coli)
mutS homolog 2, colon cancer, nonpolyposis type 1
mutS homolog II
LCFS2 protein
mutS homolog 2, colon cancer, nonpolyposis type 1 (E. coli)
COCA I gene
Lynch cancer family syndrome 2 protein
Lynch cancer family syndrome 2 gene
COCA1 gene
colon cancer, nonpolyposis type 1 gene
colon cancer, nonpolyposis type I gene
FCC I gene
FCC1 gene
HNPCC I gene
HNPCC1 gene
LCFS2 gene
COCA I
colon cancer, nonpolyposis type 1
colon cancer, nonpolyposis type I
FCC I
HNPCC I
HNPCC1s
HNPCC Is

Organism Homo sapiens
Mus musculus
Rattus norvegicus

OMIM ID 609309
120435
158320
276300
114030
137800
162200
114400

Unigene ID Hs.597656
Mm.4619
Rn.3174
Mm.471165

KEGG ID hsa:4436
mmu:17685
rno:81709

Swiss-Prot Accession B4E2Z2
P43246
P43247
Q3TZI5
P54275
O75488
Q0ZAI9
Q0ZAJ0
Q0ZAJ1
Q0ZAJ2
Q53FK0
Q53GS1
Q53RU4
Q6VBB7
Q80V79

GO ID 0043531
0005524
0016887
0003677
0008094
0032405
0000403
0019237
0032139
0032181
0000406
0003690
0019899
0000400
0032137
0000404
0000287
0030983
0032357
0008022
0042803
0019901
0032142
0032143
0003697
0030183
0019724
0006281
0007050
0008340
0006302
0007281
0001701
0031573
0042771
0045190
0043570
0008584
0006311
0000710
0006298
0045910
0043524
0045128
0006119
0051096
0006301
0010224
0010165
0043200
0042493
0014070
0016446
0016447
0007283
0032301
0032302
0000228
0003684
0000166
0006200
0006915
0007049
0043066
0006974
0002204
0005634
0032138
0004422
0006928
0045786
0006164
0006284

PIR ID S53608
I64819
JC6184

Swiss-Prot ID MSH2_MOUSE
MSH2_HUMAN
MSH2_RAT
Q3TZI5_MOUSE

Cell Localization Nucleus

IPI ID IPI00118158
IPI00017303
IPI00211849
IPI00783458
IPI00816513
IPI00783348
IPI00893933
IPI00892635

Mouse chromosome position 17 45.9 cM

Rat chromosome position 6q12

Homologene ID 210

MGI ID 101816

RGD ID 620786

Primary Cell Localization Nucleus