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TCF7L2 R397W [nucleoplasm]
Stable Identifier
R-HSA-5339696
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
nucleoplasm
Icon
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of signal transduction by growth factor receptors and second messengers (Homo sapiens)
Signaling by WNT in cancer (Homo sapiens)
Signaling by TCF7L2 mutants (Homo sapiens)
TFC7L2 mutants don't bind CTBP (Homo sapiens)
TCF7L2 mutants [nucleoplasm] (Homo sapiens)
TCF7L2 R397W [nucleoplasm] (Homo sapiens)
Literature References
PubMed ID
Title
Journal
Year
18621708
A genome-wide RNAi screen for Wnt/beta-catenin pathway components identifies unexpected roles for TCF transcription factors in cancer
Dodge, M
,
Lum, L
,
Gundapaneni, D
,
Michnoff, C
,
Tang, W
,
Roth, M
Proc. Natl. Acad. Sci. U.S.A.
2008
External Reference Information
External Reference
UniProt:Q9NQB0 TCF7L2
Gene Names
TCF7L2, TCF4
Chain
chain:1-619
Reference Genes
BioGPS Gene:6934 TCF7L2
COSMIC (genes):TCF7L2 TCF7L2
CTD Gene:6934 TCF7L2
dbSNP Gene:6934 TCF7L2
ENSEMBL:ENSG00000148737 TCF7L2
ENSEMBL_homo_sapiens_GENE:ENSG00000148737.18 TCF7L2
HGNC:11641 TCF7L2
KEGG Gene (Homo sapiens):6934 TCF7L2
Monarch:6934 TCF7L2
NCBI Gene:6934 TCF7L2
OMIM:602228 TCF7L2
UCSC:Q9NQB0 TCF7L2
Reference Transcript
RefSeq:NM_001146283.1 TCF7L2
RefSeq:XM_005270084.1 TCF7L2
RefSeq:NM_001198531.1 TCF7L2
RefSeq:NM_001198528.1 TCF7L2
RefSeq:XM_017016592.1 TCF7L2
RefSeq:NM_001146274.1 TCF7L2
RefSeq:NM_001198526.1 TCF7L2
RefSeq:XM_005270103.1 TCF7L2
RefSeq:NM_001146286.1 TCF7L2
RefSeq:XM_005270096.2 TCF7L2
RefSeq:NM_001146284.1 TCF7L2
RefSeq:XM_005270089.1 TCF7L2
RefSeq:XM_017016593.1 TCF7L2
Other Identifiers
11746313_a_at
11746314_s_at
11746315_x_at
11746404_a_at
11747829_x_at
11751102_x_at
11755181_a_at
16709333
212759_PM_s_at
212759_s_at
212761_PM_at
212761_at
212762_PM_s_at
212762_s_at
216035_PM_x_at
216035_x_at
216037_PM_x_at
216037_x_at
216511_PM_s_at
216511_s_at
32025_at
3264622
3264623
3264624
3264626
3264627
3264633
3264652
3264659
3264685
3264689
3264692
3264696
3264697
3264698
3264699
3264708
3264710
3264712
3264714
3264722
3264723
3264724
3264725
3264726
48528_at
6934
7930537
A_14_P125103
A_14_P133398
A_23_P127013
A_23_P389588
A_24_P921823
A_33_P3377304
GE83165
GO:0000122
GO:0000785
GO:0000976
GO:0000978
GO:0000981
GO:0001568
GO:0003677
GO:0003700
GO:0005515
GO:0005634
GO:0005654
GO:0005694
GO:0005975
GO:0006351
GO:0006355
GO:0006357
GO:0006790
GO:0008013
GO:0009749
GO:0010718
GO:0010909
GO:0012501
GO:0016055
GO:0016605
GO:0016922
GO:0019901
GO:0023052
GO:0030154
GO:0031016
GO:0032024
GO:0032092
GO:0032350
GO:0032993
GO:0042593
GO:0043226
GO:0043433
GO:0043565
GO:0043570
GO:0045295
GO:0045444
GO:0045721
GO:0045892
GO:0045944
GO:0048625
GO:0048660
GO:0048856
GO:0050679
GO:0051897
GO:0060070
GO:0061629
GO:0070016
GO:0070369
GO:0071664
GO:0090090
GO:0140110
GO:1900182
GO:1901135
GO:1990841
GO:1990907
GO:2000675
GO:2001237
HMNXSV003004532
HMNXSV003007299
HMNXSV003057192
Hs.173638.0.S1_3p_s_at
Hs.173638.0.S2_3p_s_at
Hs.173638.0.S3_3p_a_at
Hs.173638.0.S3_3p_at
Hs.173638.1.S1_3p_x_at
Hs.173638.2.S1_3p_a_at
Hs.173638.2.S1_3p_x_at
Hs.283857.0.S1_3p_s_at
ILMN_1672486
TC10000820.hg
TC10002300.hg
Y11306_rna1_at
Participates
as a candidate of
TCF7L2 mutants [nucleoplasm] (Homo sapiens)
Other forms of this molecule
TCF7L2 K485fs*25 [nucleoplasm]
pT201,T212-TCF7L2 [nucleoplasm]
TCF7L2 [nucleoplasm]
Modified Residues
Name
L-arginine 397 replaced with L-tryptophan
Coordinate
397
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
colorectal cancer
DOID:9256
Cross References
RefSeq
XP_016872082.1
,
NP_001139758.1
,
XP_016872081.1
,
XP_005270160.1
,
NP_001185455.1
,
XP_005270153.1
,
NP_001185460.1
,
XP_005270141.1
,
NP_001185457.1
,
NP_001139746.1
,
NP_001139755.1
,
NP_001139756.1
,
XP_005270146.1
OpenTargets
ENSG00000148737
GeneCards
Q9NQB0
HPA
ENSG00000148737-TCF7L2
Ensembl
ENSP00000486891
,
ENSP00000358404
,
ENST00000369397
,
ENST00000538897
,
ENSP00000348274
,
ENST00000355717
,
ENSP00000344823
,
ENSP00000347949
,
ENST00000355995
,
ENSP00000446172
,
ENSG00000148737
,
ENST00000627217
,
ENST00000352065
PRO
Q9NQB0
Pharos - Targets
Q9NQB0
Orphanet
24970
PDB
2GL7
,
1JDH
,
1JPW
Interactors (6)
Accession
#Entities
Entities
Confidence Score
Evidence (IntAct)
UniProt:P35222 CTNNB1
20
CTNNB1 S45A [cytosol]
(R-HSA-9663982)
CTNNB1 S45F [cytosol]
(R-HSA-4791268)
CTNNB1 S45C [cytosol]
(R-HSA-9663983)
CTNNB1 S45Y [cytosol]
(R-HSA-9663975)
CTNNB1 S45N [cytosol]
(R-HSA-9663984)
CTNNB1 S45P [cytosol]
(R-HSA-4791272)
pT41,S45-CTNNB1 S37P [cytosol]
(R-HSA-9663981)
pT41,S45-CTNNB1 S37F [cytosol]
(R-HSA-4839621)
pT41,S45-CTNNB1 S37A [cytosol]
(R-HSA-4839619)
pT41,S45-CTNNB1 S37Y [cytosol]
(R-HSA-9663978)
pT41,S45-CTNNB1 S37C [cytosol]
(R-HSA-4839617)
pS37,T41,S45-CTNNB1 S33A [cytosol]
(R-HSA-9663976)
pS37,T41,S45-CTNNB1 S33T [cytosol]
(R-HSA-9663977)
pS37,T41,S45-CTNNB1 S33C [cytosol]
(R-HSA-4839630)
pS37,T41,S45-CTNNB1 S33F [cytosol]
(R-HSA-4839628)
pS37,T41,S45-CTNNB1 S33P [cytosol]
(R-HSA-4839626)
pS37,T41,S45-CTNNB1 S33Y [cytosol]
(R-HSA-4839625)
pS45-CTNNB1 T41N [cytosol]
(R-HSA-9663980)
pS45-CTNNB1 T41A [cytosol]
(R-HSA-4836868)
pS45-CTNNB1 T41I [cytosol]
(R-HSA-4839612)
0.97
27
UniProt:Q13761 RUNX3
7
RUNX3 [nucleoplasm]
(R-HSA-8865393)
RUNX3 [cytosol]
(R-HSA-8937797)
Ac-K94,K171-RUNX3 [nucleoplasm]
(R-HSA-8951965)
PolyUb-K94,K148-RUNX3 [cytosol]
(R-HSA-8952400)
PolyUb-K94,K148-RUNX3 [nucleoplasm]
(R-HSA-8952387)
p-Y-RUNX3 [cytosol]
(R-HSA-8937805)
PolyUb-RUNX3 [nucleoplasm]
(R-HSA-8952417)
0.656
14
UniProt:Q08050 FOXM1
3
p-T611,S730,S739-FOXM1 [nucleoplasm]
(R-HSA-4088133)
p-T611-FOXM1 [nucleoplasm]
(R-HSA-4088026)
FOXM1 [nucleoplasm]
(R-HSA-4088019)
0.612
7
UniProt:Q14526 HIC1
2
monoSUMO1-K333-HIC1 [nucleoplasm]
(R-HSA-4090368)
HIC1 [nucleoplasm]
(R-HSA-4090364)
0.61
6
UniProt:P09874 PARP1
4
polySUMO2,3-K203,K486-PARP1 [nucleoplasm]
(R-HSA-4551617)
monoSUMO1-K203,K486-PARP1 [nucleoplasm]
(R-HSA-4551686)
PAR-PARP1 [nucleoplasm]
(R-HSA-5651713)
PARP1 [nucleoplasm]
(R-HSA-201568)
0.597
6
UniProt:Q9UER7 DAXX
13
monoSUMO1-K630,K631-DAXX [nucleoplasm]
(R-HSA-4086086)
DAXX L98Vfs*13 [nucleoplasm]
(R-HSA-9673102)
DAXX R48Vfs*93 [nucleoplasm]
(R-HSA-9673103)
DAXX C74* [nucleoplasm]
(R-HSA-9673096)
DAXX S138* [nucleoplasm]
(R-HSA-9673081)
DAXX H26Tfs*118 [nucleoplasm]
(R-HSA-9673114)
DAXX E104* [nucleoplasm]
(R-HSA-9673078)
DAXX E72Nfs*72 [nucleoplasm]
(R-HSA-9673110)
DAXX C106* [nucleoplasm]
(R-HSA-9673079)
DAXX A103Sfs*40 [nucleoplasm]
(R-HSA-9673121)
DAXX K56* [nucleoplasm]
(R-HSA-9673089)
DAXX A36Qfs*108 [nucleoplasm]
(R-HSA-9673105)
DAXX [nucleoplasm]
(R-HSA-3222068)
0.543
5
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