TCF7L1 (transcription factor 7 like 1) - Rat Genome Database
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Gene: TCF7L1 (transcription factor 7 like 1) Homo sapiens
Analyze
Symbol: TCF7L1
Name: transcription factor 7 like 1
RGD ID: 1323251
HGNC Page HGNC
Description: Exhibits sequence-specific double-stranded DNA binding activity. Predicted to be involved in several processes, including axial mesoderm morphogenesis; regulation of transcription, DNA-templated; and somatic stem cell population maintenance. Localizes to cytosol and nucleoplasm.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: HMG box transcription factor 3; HMG-box transcription factor TCF-3; TCF-3; TCF3; transcription factor 7-like 1; transcription factor 7-like 1 (T-cell specific, HMG-box)
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl285,133,392 - 85,310,387 (+)EnsemblGRCh38hg38GRCh38
GRCh38285,133,392 - 85,310,387 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37285,360,583 - 85,537,511 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36285,214,245 - 85,391,016 (+)NCBINCBI36hg18NCBI36
Build 34285,272,391 - 85,449,162NCBI
Celera285,189,038 - 85,365,500 (+)NCBI
Cytogenetic Map2p11.2NCBI
HuRef285,257,850 - 85,434,099 (+)NCBIHuRef
CHM1_1285,290,354 - 85,467,245 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

References

Additional References at PubMed
PMID:1741298   PMID:9916915   PMID:11085512   PMID:11136974   PMID:11238923   PMID:11266540   PMID:12477932   PMID:15327769   PMID:15489334   PMID:15815621   PMID:16565489   PMID:17234346  
PMID:17873379   PMID:18258400   PMID:19274049   PMID:19301967   PMID:19304756   PMID:19308021   PMID:19373426   PMID:19906297   PMID:20379614   PMID:20532534   PMID:21285352   PMID:21873635  
PMID:22930747   PMID:23063976   PMID:23090119   PMID:23492770   PMID:24596249   PMID:25659031   PMID:26687479   PMID:26764381   PMID:27333864   PMID:28467300   PMID:28473536   PMID:29361574  
PMID:30021253   PMID:30585266   PMID:30811526   PMID:31322782   PMID:31381875   PMID:31753913  


Genomics

Comparative Map Data
TCF7L1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl285,133,392 - 85,310,387 (+)EnsemblGRCh38hg38GRCh38
GRCh38285,133,392 - 85,310,387 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37285,360,583 - 85,537,511 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36285,214,245 - 85,391,016 (+)NCBINCBI36hg18NCBI36
Build 34285,272,391 - 85,449,162NCBI
Celera285,189,038 - 85,365,500 (+)NCBI
Cytogenetic Map2p11.2NCBI
HuRef285,257,850 - 85,434,099 (+)NCBIHuRef
CHM1_1285,290,354 - 85,467,245 (+)NCBICHM1_1
Tcf7l1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39672,603,354 - 72,766,028 (-)NCBIGRCm39mm39
GRCm38672,626,371 - 72,789,045 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl672,626,378 - 72,789,254 (-)EnsemblGRCm38mm10GRCm38
MGSCv37672,576,374 - 72,738,950 (-)NCBIGRCm37mm9NCBIm37
MGSCv36672,555,889 - 72,718,465 (-)NCBImm8
Celera674,727,941 - 74,893,703 (-)NCBICelera
Cytogenetic Map6C1NCBI
cM Map632.27NCBI
Tcf7l1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Rnor_6.04100,492,796 - 100,660,401 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl4100,491,798 - 100,660,140 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.04165,263,179 - 165,427,206 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.44106,128,203 - 106,149,229 (-)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.14106,372,784 - 106,393,874 (-)NCBI
Celera493,833,646 - 93,998,059 (-)NCBICelera
Cytogenetic Map4q31NCBI
Tcf7l1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554242,137,865 - 2,286,181 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554242,139,576 - 2,286,183 (-)NCBIChiLan1.0ChiLan1.0
TCF7L1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.12A86,739,422 - 86,914,829 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2A86,739,417 - 86,913,905 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v02A85,186,660 - 85,363,033 (+)NCBIMhudiblu_PPA_v0panPan3
TCF7L1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1 Ensembl1739,699,958 - 39,858,182 (-)EnsemblCanFam3.1canFam3CanFam3.1
CanFam3.11739,699,958 - 39,859,167 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Tcf7l1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
SpeTri2.0NW_0049367121,848,478 - 1,962,644 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
TCF7L1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1359,438,152 - 59,458,988 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2362,435,512 - 62,533,066 (-)NCBISscrofa10.2Sscrofa10.2susScr3
TCF7L1
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11421,849,585 - 22,028,147 (-)NCBI
Tcf7l1
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462474917,804,630 - 17,956,504 (-)NCBI

Position Markers
D2S2333  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37285,488,173 - 85,488,426UniSTSGRCh37
Build 36285,341,684 - 85,341,937RGDNCBI36
Celera285,316,486 - 85,316,739RGD
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map2p12-q22UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map2p12-p11.1UniSTS
HuRef285,384,880 - 85,385,137UniSTS
Marshfield Genetic Map2103.16UniSTS
Marshfield Genetic Map2103.16RGD
Genethon Genetic Map2107.7UniSTS
TNG Radiation Hybrid Map253524.0UniSTS
deCODE Assembly Map2108.81UniSTS
Stanford-G3 RH Map23607.0UniSTS
GeneMap99-G3 RH Map23518.0UniSTS
RH45510  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37285,414,819 - 85,415,009UniSTSGRCh37
Build 36285,268,330 - 85,268,520RGDNCBI36
Celera285,243,135 - 85,243,325RGD
Cytogenetic Map2p11.2UniSTS
HuRef285,311,527 - 85,311,717UniSTS
GeneMap99-GB4 RH Map2295.38UniSTS
NCBI RH Map2460.4UniSTS
RH103338  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37285,394,224 - 85,394,361UniSTSGRCh37
Build 36285,247,735 - 85,247,872RGDNCBI36
Celera285,222,538 - 85,222,675RGD
Cytogenetic Map2p11.2UniSTS
HuRef285,290,924 - 85,291,061UniSTS
GeneMap99-GB4 RH Map2295.38UniSTS
DXS7905  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37X119,261,422 - 119,261,506UniSTSGRCh37
GRCh37285,373,023 - 85,374,093UniSTSGRCh37
Build 36X119,145,450 - 119,145,534RGDNCBI36
Celera285,201,332 - 85,202,400UniSTS
CeleraX119,697,259 - 119,697,343RGD
Cytogenetic Map2p11.2UniSTS
HuRefX108,713,789 - 108,713,873UniSTS
HuRef285,269,725 - 85,270,795UniSTS
G59683  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37285,414,820 - 85,414,925UniSTSGRCh37
Build 36285,268,331 - 85,268,436RGDNCBI36
Celera285,243,136 - 85,243,241RGD
Cytogenetic Map2p11.2UniSTS
HuRef285,311,528 - 85,311,633UniSTS
TNG Radiation Hybrid Map253491.0UniSTS
SHGC-146364  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37285,491,859 - 85,492,186UniSTSGRCh37
Build 36285,345,370 - 85,345,697RGDNCBI36
Celera285,320,172 - 85,320,499RGD
Cytogenetic Map2p11.2UniSTS
HuRef285,388,570 - 85,388,897UniSTS
TNG Radiation Hybrid Map253528.0UniSTS
SHGC-146832  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37285,504,653 - 85,504,961UniSTSGRCh37
Build 36285,358,164 - 85,358,472RGDNCBI36
Celera285,332,968 - 85,333,276RGD
Cytogenetic Map2p11.2UniSTS
HuRef285,401,366 - 85,401,674UniSTS
TNG Radiation Hybrid Map253577.0UniSTS
SHGC-148128  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37285,492,164 - 85,492,479UniSTSGRCh37
Build 36285,345,675 - 85,345,990RGDNCBI36
Celera285,320,477 - 85,320,792RGD
Cytogenetic Map2p11.2UniSTS
HuRef285,388,875 - 85,389,190UniSTS
TNG Radiation Hybrid Map253524.0UniSTS
D2S2793  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37285,457,320 - 85,457,438UniSTSGRCh37
Build 36285,310,831 - 85,310,949RGDNCBI36
Celera285,285,635 - 85,285,753RGD
Cytogenetic Map2p11.2UniSTS
HuRef285,354,027 - 85,354,145UniSTS
TNG Radiation Hybrid Map253513.0UniSTS
Stanford-G3 RH Map23583.0UniSTS
PMC31284P1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37285,533,329 - 85,533,665UniSTSGRCh37
Build 36285,386,840 - 85,387,176RGDNCBI36
Celera285,361,318 - 85,361,654RGD
Cytogenetic Map2p11.2UniSTS
TCF7L1_2208  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37285,536,737 - 85,537,534UniSTSGRCh37
Build 36285,390,248 - 85,391,045RGDNCBI36
Celera285,364,732 - 85,365,529RGD
RH45456  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37285,536,406 - 85,536,616UniSTSGRCh37
Build 36285,389,917 - 85,390,127RGDNCBI36
Celera285,364,401 - 85,364,611RGD
Cytogenetic Map2p11.2UniSTS
GeneMap99-GB4 RH Map2295.34UniSTS
NCBI RH Map2460.4UniSTS
A006A34  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37285,537,237 - 85,537,374UniSTSGRCh37
Build 36285,390,748 - 85,390,885RGDNCBI36
Celera285,365,232 - 85,365,369RGD
Cytogenetic Map2p11.2UniSTS
HuRef285,433,825 - 85,433,962UniSTS
GeneMap99-GB4 RH Map2295.28UniSTS
D2S2755  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37285,522,681 - 85,522,812UniSTSGRCh37
Build 36285,376,192 - 85,376,323RGDNCBI36
Celera285,350,656 - 85,350,787RGD
Cytogenetic Map2p11.2UniSTS
HuRef285,419,021 - 85,419,152UniSTS
TNG Radiation Hybrid Map253545.0UniSTS
Stanford-G3 RH Map23572.0UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1097
Count of miRNA genes:656
Interacting mature miRNAs:708
Transcripts:ENST00000282111, ENST00000442813, ENST00000490744, ENST00000494519
Prediction methods:Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 1764 1729 951 226 331 91 3467 1212 948 164 1323 1409 144 1 1203 2154 3
Low 643 1174 767 397 1107 373 889 981 2780 247 129 170 31 1 634 2 2
Below cutoff 28 84 8 1 453 1 1 3 6 8 8 31 1

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000282111   ⟹   ENSP00000282111
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl285,133,392 - 85,310,387 (+)Ensembl
RefSeq Acc Id: ENST00000442813   ⟹   ENSP00000388984
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl285,213,623 - 85,302,494 (+)Ensembl
RefSeq Acc Id: ENST00000490744
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl285,303,393 - 85,304,364 (+)Ensembl
RefSeq Acc Id: ENST00000494519
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl285,134,368 - 85,167,373 (+)Ensembl
RefSeq Acc Id: NM_031283   ⟹   NP_112573
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38285,133,392 - 85,310,387 (+)NCBI
GRCh37285,360,583 - 85,537,511 (+)ENTREZGENE
Build 36285,214,245 - 85,391,016 (+)NCBI Archive
HuRef285,257,850 - 85,434,099 (+)ENTREZGENE
CHM1_1285,290,354 - 85,467,245 (+)NCBI
Sequence:
RefSeq Acc Id: XM_006712109   ⟹   XP_006712172
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38285,133,670 - 85,310,387 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_112573   ⟸   NM_031283
- UniProtKB: Q9HCS4 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_006712172   ⟸   XM_006712109
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: ENSP00000282111   ⟸   ENST00000282111
RefSeq Acc Id: ENSP00000388984   ⟸   ENST00000442813
Protein Domains
CTNNB1_binding

Promoters
RGD ID:6860874
Promoter ID:EPDNEW_H3602
Type:initiation region
Name:TCF7L1_1
Description:transcription factor 7 like 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38285,133,414 - 85,133,474EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 2p12-11.2(chr2:77025216-90282666)x3 copy number gain See cases [RCV000134786] Chr2:77025216..90282666 [GRCh38]
Chr2:77252342..91619262 [GRCh37]
Chr2:77105850..90982989 [NCBI36]
Chr2:2p12-11.2
pathogenic
GRCh38/hg38 2p16.3-11.2(chr2:47620388-86702722)x3 copy number gain See cases [RCV000137586] Chr2:47620388..86702722 [GRCh38]
Chr2:47847527..86929845 [GRCh37]
Chr2:47701031..86783356 [NCBI36]
Chr2:2p16.3-11.2
uncertain significance
GRCh38/hg38 2p11.2(chr2:85179123-85369264)x3 copy number gain See cases [RCV000140134] Chr2:85179123..85369264 [GRCh38]
Chr2:85406246..85596387 [GRCh37]
Chr2:85259757..85449898 [NCBI36]
Chr2:2p11.2
uncertain significance
GRCh38/hg38 2p11.2(chr2:85014686-88826619)x1 copy number loss See cases [RCV000141948] Chr2:85014686..88826619 [GRCh38]
Chr2:85241809..89126132 [GRCh37]
Chr2:85095320..88907247 [NCBI36]
Chr2:2p11.2
pathogenic
GRCh38/hg38 2p25.1-11.2(chr2:7495123-87705899)x3 copy number gain See cases [RCV000141494] Chr2:7495123..87705899 [GRCh38]
Chr2:7635254..88005418 [GRCh37]
Chr2:7552705..87786533 [NCBI36]
Chr2:2p25.1-11.2
benign
GRCh37/hg19 2p15-11.2(chr2:62245236-86978895)x3 copy number gain See cases [RCV000448688] Chr2:62245236..86978895 [GRCh37]
Chr2:2p15-11.2
pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384) copy number gain See cases [RCV000512056] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3
pathogenic
GRCh37/hg19 2p13.1-11.2(chr2:74365484-89129064)x1 copy number loss See cases [RCV000510763] Chr2:74365484..89129064 [GRCh37]
Chr2:2p13.1-11.2
pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3 copy number gain See cases [RCV000511212] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3
pathogenic
GRCh37/hg19 2p12-11.2(chr2:82517612-86262705)x3 copy number gain not provided [RCV000682150] Chr2:82517612..86262705 [GRCh37]
Chr2:2p12-11.2
uncertain significance
Single allele inversion not provided [RCV000714264] Chr2:40608411..146900718 [GRCh37]
Chr2:2p22.1-q22.3
likely pathogenic
GRCh37/hg19 2p13.1-11.2(chr2:74527522-89125488)x1 copy number loss not provided [RCV000682167] Chr2:74527522..89125488 [GRCh37]
Chr2:2p13.1-11.2
pathogenic
Single allele duplication not provided [RCV000677942] Chr2:63671346..85698002 [GRCh37]
Chr2:2p15-11.2
pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:15672-243101834)x3 copy number gain not provided [RCV000752804] Chr2:15672..243101834 [GRCh37]
Chr2:2p25.3-q37.3
pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:14238-243048760)x3 copy number gain not provided [RCV000752802] Chr2:14238..243048760 [GRCh37]
Chr2:2p25.3-q37.3
pathogenic
NM_031283.3(TCF7L1):c.478T>A (p.Ser160Thr) single nucleotide variant not provided [RCV000966802] Chr2:85283531 [GRCh38]
Chr2:85510654 [GRCh37]
Chr2:2p11.2
benign
GRCh37/hg19 2p11.2(chr2:85357332-85685465)x3 copy number gain not provided [RCV001005290] Chr2:85357332..85685465 [GRCh37]
Chr2:2p11.2
uncertain significance
GRCh37/hg19 2p12-11.2(chr2:77907114-87330965)x1 copy number loss not provided [RCV000846587] Chr2:77907114..87330965 [GRCh37]
Chr2:2p12-11.2
pathogenic
GRCh37/hg19 2p11.2(chr2:85401388-85615492)x3 copy number gain not provided [RCV001005291] Chr2:85401388..85615492 [GRCh37]
Chr2:2p11.2
uncertain significance

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:11640 AgrOrtholog
COSMIC TCF7L1 COSMIC
Ensembl Genes ENSG00000152284 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000282111 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000388984 UniProtKB/TrEMBL
Ensembl Transcript ENST00000282111 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000442813 UniProtKB/TrEMBL
Gene3D-CATH 1.10.30.10 UniProtKB/Swiss-Prot
  4.10.900.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000152284 GTEx
HGNC ID HGNC:11640 ENTREZGENE
Human Proteome Map TCF7L1 Human Proteome Map
InterPro Catenin_binding_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  CTNNB1-bd_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HMG_box_dom UniProtKB/Swiss-Prot
  HMG_box_dom_sf UniProtKB/Swiss-Prot
  TCF/LEF UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Tcf7l1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:83439 UniProtKB/Swiss-Prot
NCBI Gene 83439 ENTREZGENE
OMIM 604652 OMIM
PANTHER PTHR10373 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR10373:SF25 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam CTNNB1_binding UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HMG_box UniProtKB/Swiss-Prot
PharmGKB PA36393 PharmGKB
PROSITE HMG_BOX_2 UniProtKB/Swiss-Prot
SMART HMG UniProtKB/Swiss-Prot
Superfamily-SCOP SSF47095 UniProtKB/Swiss-Prot
UniProt C9JPE3_HUMAN UniProtKB/TrEMBL
  Q53T87_HUMAN UniProtKB/TrEMBL
  Q9HCS4 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary Q53R97 UniProtKB/Swiss-Prot
  Q6PD70 UniProtKB/Swiss-Prot
  Q9NP00 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-02-10 TCF7L1  transcription factor 7 like 1    transcription factor 7-like 1 (T-cell specific, HMG-box)  Symbol and/or name change 5135510 APPROVED