TCF12 (transcription factor 12)

2003-07-01   Goran Stenman  

Lundberg Laboratory for Cancer Research, Department of Pathology, Goteborg University, Sahlgrenska University Hospital, SE-413 45 Goteborg, Sweden

Identity

HGNC
LOCATION
15q21.3
LOCUSID
ALIAS
CRS3,HEB,HTF4,HsT17266,TCF-12,bHLHb20,p64
FUSION GENES

DNA/RNA

Description

spans 370 kb; 21 exons.

Transcription

two alternatively spliced transcripts of 4745 bp and 4077 bp.

Proteins

Description

682 aa, 73 kDa; serine rich N-terminus containing a potential leuzine zipper domain; C-terminus containing a bHLH-domain as well as a class A-specific domain.

Expression

ubiquitous

Localisation

nuclear

Function

basic helix-loop-helix (bHLH) transcription factor belonging to the class A family; acts as a general negative regulator of cell proliferation; binds specifically to oligomers of E-box motifs; forms heterodimers with other bHLH proteins of both class A and class B, e.g. E2A, TAL1, myogenin and MyoD; implicated in myogenesis, hematopoiesis and neurogenesis.

Homology

Implicated in

Entity name
Disease
rare type of sarcoma (2.3% of all soft tissue sarcomas) characteristically involving the deep, soft tissues of the extremities; morphological resemblance to embryonic cartilage.
Hybrid gene
TCF12-TEC
Fusion protein
N-terminal domain of TCF12 fused to the entire TEC protein; the translocation separates the N-terminal of TCF12 from the bHLH domain as well as from a potential leucine zipper domain; the N-terminal of TCF12 shows no sequence homology to the N-terminals of EWSR1 or TAF2N.

Bibliography

Pubmed IDLast YearTitleAuthors

Other Information

Locus ID:

NCBI: 6938
MIM: 600480
HGNC: 11623
Ensembl: ENSG00000140262

Variants:

dbSNP: 6938
ClinVar: 6938
TCGA: ENSG00000140262
COSMIC: TCF12

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000140262ENST00000267811Q99081
ENSG00000140262ENST00000267811A0A024R5T1
ENSG00000140262ENST00000333725Q99081
ENSG00000140262ENST00000333725A0A024R5Z0
ENSG00000140262ENST00000343827Q99081
ENSG00000140262ENST00000438423Q99081
ENSG00000140262ENST00000438423A0A024R5Z0
ENSG00000140262ENST00000537840Q99081
ENSG00000140262ENST00000543579F5GY10
ENSG00000140262ENST00000557843Q99081
ENSG00000140262ENST00000557843A0A024R5T1
ENSG00000140262ENST00000557947H0YNQ5
ENSG00000140262ENST00000559609B4DGI9
ENSG00000140262ENST00000559703H0YNP8
ENSG00000140262ENST00000559710B4DZP2
ENSG00000140262ENST00000560836H3BNF4
ENSG00000140262ENST00000560948H3BRK2
ENSG00000140262ENST00000561152H0YML2

Expression (GTEx)

0
5
10
15
20
25
30
35
40

Pathways

PathwaySourceExternal ID
Developmental BiologyREACTOMER-HSA-1266738
MyogenesisREACTOMER-HSA-525793
CDO in myogenesisREACTOMER-HSA-375170

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
376801492024Lncrna CASC15 Activated By TCF12 Promote Colorectal Cancer Progression via EMT.0
376801492024Lncrna CASC15 Activated By TCF12 Promote Colorectal Cancer Progression via EMT.0
359947502023Auricles Anomalies in Patients With a TCF12 Gene Mutation.0
363775082023RNA-binding protein DHX9 promotes glioma growth and tumor-associated macrophages infiltration via TCF12.13
369169302023Circular RNA hsa_circ_0002938 (circCRIM1) promotes the progression of esophageal squamous cell carcinoma by upregulating transcription factor 12.1
370676452023Nuclear Tubulin Enhances CXCR4 Transcription and Promotes Chemotaxis Through TCF12 Transcription Factor in human Hematopoietic Stem Cells.0
359947502023Auricles Anomalies in Patients With a TCF12 Gene Mutation.0
363775082023RNA-binding protein DHX9 promotes glioma growth and tumor-associated macrophages infiltration via TCF12.13
369169302023Circular RNA hsa_circ_0002938 (circCRIM1) promotes the progression of esophageal squamous cell carcinoma by upregulating transcription factor 12.1
370676452023Nuclear Tubulin Enhances CXCR4 Transcription and Promotes Chemotaxis Through TCF12 Transcription Factor in human Hematopoietic Stem Cells.0
341215152022miR-218-5p inhibits the malignant progression of glioma via targeting TCF12.1
344249512022Evaluation of dental maturity in Muenke syndrome, Saethre-Chotzen syndrome, and TCF12-related craniosynostosis.1
349041782022Craniofacial morphology and growth in Muenke syndrome, Saethre-Chotzen syndrome, and TCF12-related craniosynostosis.1
341215152022miR-218-5p inhibits the malignant progression of glioma via targeting TCF12.1
344249512022Evaluation of dental maturity in Muenke syndrome, Saethre-Chotzen syndrome, and TCF12-related craniosynostosis.1

Citation

Goran Stenman

TCF12 (transcription factor 12)

Atlas Genet Cytogenet Oncol Haematol. 2003-07-01

Online version: http://atlasgeneticsoncology.org/gene/406/favicon/img/teaching-explorer/