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MUTYH-3 R227W [nucleoplasm]
Stable Identifier
R-HSA-9606261
Type
Genes and Transcripts [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
nucleoplasm
Synonyms
MUTYH-3 Arg227Trp, MUTYH alpha-3 R227W, MUTYH alpha-3 Arg227Trp
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of DNA repair (Homo sapiens)
Diseases of Base Excision Repair (Homo sapiens)
Defective Base Excision Repair Associated with MUTYH (Homo sapiens)
Defective MUTYH substrate binding (Homo sapiens)
Defective MUTYH mutants do not bind adenine mispaired with 8-oxoguanine (Homo sapiens)
MUTYH binding LOF mutants [nucleoplasm] (Homo sapiens)
MUTYH-3 R227W [nucleoplasm] (Homo sapiens)
Defective MUTYH substrate processing (Homo sapiens)
Defective MUTYH mutants do not cleave adenine mispaired with 8-oxoguanine (Homo sapiens)
MUTYH LOF mutants:(8oxoG:Ade)-dsDNA [nucleoplasm] (Homo sapiens)
MUTYH LOF mutants [nucleoplasm] (Homo sapiens)
MUTYH-3 R227W [nucleoplasm] (Homo sapiens)
Literature References
PubMed ID
Title
Journal
Year
15673720
Functional characterization of two human MutY homolog (hMYH) missense mutations (R227W and V232F) that lie within the putative hMSH6 binding domain and are associated with hMYH polyposis
Sampson, JR
,
Wilson, TM
,
Bai, H
,
Cheadle, JP
,
Jones, S
,
Guan, X
,
Lu, AL
Nucleic Acids Res.
2005
External Reference Information
External Reference
UniProt:Q9UIF7-3 MUTYH
Gene Names
MUTYH, MYH
Other Identifiers
11734568_a_at
16686401
207727_PM_s_at
207727_s_at
2410112
2410113
2410120
2410123
2410124
2410126
2410127
2410128
2410130
2410131
2410133
2410134
2410135
2410137
2410139
2410141
2410142
2410143
2410144
2410145
2410147
2410149
2410150
2410151
2410152
2410153
4595
489_at
490_g_at
7915695
A_23_P51660
GE80793
GO:0000701
GO:0003677
GO:0003824
GO:0005515
GO:0005634
GO:0005654
GO:0005739
GO:0006281
GO:0006284
GO:0006298
GO:0006950
GO:0006974
GO:0008152
GO:0012501
GO:0016787
GO:0016798
GO:0019104
GO:0032357
GO:0032407
GO:0034039
GO:0035485
GO:0043226
GO:0045007
GO:0046872
GO:0051536
GO:0051539
GO:0060546
GO:0140097
HMNXSV003054539
ILMN_2277537
ILMN_2336970
PH_hs_0013965
U63329_at
g6912519_3p_a_at
Participates
as a member of
MUTYH binding LOF mutants [nucleoplasm] (Homo sapiens)
MUTYH LOF mutants [nucleoplasm] (Homo sapiens)
Other forms of this molecule
MUTYH-3 A359V [nucleoplasm]
MUTYH-3 R171W [nucleoplasm]
MUTYH-3 G272E [nucleoplasm]
MUTYH-3 Q324R [nucleoplasm]
MUTYH-3 V232F [nucleoplasm]
MUTYH-3 A368fs*26 [nucleoplasm]
MUTYH-3 E466del [nucleoplasm]
MUTYH-3 P391L [nucleoplasm]
MUTYH-3 Q377* [nucleoplasm]
MUTYH-3 A459D [nucleoplasm]
MUTYH-3 W138_M139insIW [nucleoplasm]
MUTYH-3 R231H [nucleoplasm]
MUTYH-3 Y165C [nucleoplasm]
MUTYH-3 E466* [nucleoplasm]
MUTYH-3 R260Q [nucleoplasm]
MUTYH-3 Q324H [nucleoplasm]
MUTYH-3 G382D [nucleoplasm]
MUTYH-3 Y90* [nucleoplasm]
MUTYH-3 P281L [nucleoplasm]
MUTYH-3 R231L [nucleoplasm]
MUTYH-3 R260W [nucleoplasm]
MUTYH-3 A359S [nucleoplasm]
MUTYH-3 [nucleoplasm]
Modified Residues
Name
L-arginine 227 replaced with L-tryptophan
Coordinate
227
PsiMod
L-tryptophan residue [MOD:00027]
A protein modification that effectively converts a source amino acid residue to L-tryptophan.
L-arginine removal [MOD:01632]
A protein modification that effectively removes or replaces an L-arginine.
Disease
Name
Identifier
Synonyms
familial adenomatous polyposis
DOID:0050424
adenomatous polyposis of the colon
colorectal cancer
DOID:9256
Cross References
RefSeq
XP_016856823.1
,
NP_001280124.1
,
NP_001280120.1
,
NP_001280119.1
,
XP_011539806.1
,
NP_001041637.1
,
NP_001280125.1
,
NP_001041639.1
,
NP_001280121.1
,
XP_016856824.1
,
NP_036354.1
,
NP_001121897.1
,
NP_001041638.1
,
NP_001041636.1
OpenTargets
ENSG00000132781
HPA
ENSG00000132781-MUTYH
GeneCards
Q9UIF7
Ensembl
ENST00000372110
,
ENSP00000500891
,
ENSP00000361176
,
ENST00000456914
,
ENSP00000361170
,
ENSP00000361187
,
ENST00000672818
,
ENST00000372115
,
ENST00000372104
,
ENSP00000361182
,
ENST00000448481
,
ENSP00000407590
,
ENSG00000132781
,
ENSP00000347685
,
ENSP00000346354
,
ENST00000355498
,
ENSP00000409718
,
ENST00000372098
,
ENST00000354383
PRO
Q9UIF7
Pharos - Targets
Q9UIF7
Orphanet
16490
PDB
1X51
,
3N5N
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