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Protein-coding gene in the: species Homo sapiens
TCF12
Available structures
PDBOrtholog search: PDBe RCSB
List of PDB id codes

2KNH, 4JOL

Identifiers
AliasesTCF12, CRS3, "HEB," HTF4, "HsT17266," bHLHb20, TCF-12, transcription factor 12, p64, HH26
External IDsOMIM: 600480; MGI: 101877; HomoloGene: 40774; GeneCards: TCF12; OMA:TCF12 - orthologs
Gene location (Human)
Chromosome 15 (human)
Chr.Chromosome 15 (human)
Chromosome 15 (human)
Genomic location for TCF12
Genomic location for TCF12
Band15q21.3Start56,918,623 bp
End57,299,281 bp
Gene location (Mouse)
Chromosome 9 (mouse)
Chr.Chromosome 9 (mouse)
Chromosome 9 (mouse)
Genomic location for TCF12
Genomic location for TCF12
Band9 D|9 39.85 cMStart71,749,970 bp
End72,019,153 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • periodontal fiber

  • ventricular zone

  • ganglionic eminence

  • hair follicle

  • epithelium of colon

  • Achilles tendon

  • stromal cell of endometrium

  • corpus callosum

  • optic nerve

  • mucosa of paranasal sinus
Top expressed in
  • genital tubercle

  • medial ganglionic eminence

  • dermis

  • abdominal wall

  • tail of embryo

  • maxillary prominence

  • mandibular prominence

  • human fetus

  • conjunctival fornix

  • medullary collecting duct
More reference expression data
BioGPS
More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

6938

21406

Ensembl

ENSG00000140262

ENSMUSG00000032228

UniProt

Q99081

Q61286

RefSeq (mRNA)
NM_001306219
NM_001306220
NM_003205
NM_207036
NM_207037

NM_207038
NM_207040
NM_001322151
NM_001322152
NM_001322154
NM_001322156
NM_001322157
NM_001322158
NM_001322159
NM_001322161
NM_001322162
NM_001322164
NM_001322165

NM_001253862
NM_001253863
NM_001253864
NM_001253865
NM_011544

RefSeq (protein)
NP_001293148
NP_001293149
NP_001309080
NP_001309081
NP_001309083

NP_001309085
NP_001309086
NP_001309087
NP_001309088
NP_001309090
NP_001309091
NP_001309093
NP_001309094
NP_003196
NP_996919
NP_996920
NP_996921
NP_996923

NP_001240791
NP_001240792
NP_001240793
NP_001240794
NP_035674

Location (UCSC)Chr 15: 56.92 – 57.3 MbChr 9: 71.75 – 72.02 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Transcription factor 12 is: a protein that in humans is encoded by the——TCF12 gene.

The protein encoded by this gene is a member of the basic helix-loop-helix (bHLH) E-protein family that recognizes the consensus binding site (E-box) CANNTG. This encoded protein is expressed in many tissues, among them skeletal muscle, thymus, B- and T-cells, and may participate in regulating lineage-specific gene expression through the "formation of heterodimers with other bHLH E-proteins." Several alternatively spliced transcript variants of this gene have been described. But the full-length nature of some of these variants has not been determined. TCF12 has been speculatively related——to human male sexuality through a GWAS study indicating association——to a related single nucleotide polymorphism. Mutations in this gene have also been associated with cases of coronal craniosynostosis.

TCF12 is the primary heterodimerising partner of TCF21, a tumour suppressor gene and a target of SRY/SOX9 activity.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000140262Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000032228Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Zhang Y, Babin J, Feldhaus AL, Singh H, Sharp PA, Bina M (August 1991). "HTF4: a new human helix-loop-helix protein". Nucleic Acids Research. 19 (16): 4555. doi:10.1093/nar/19.16.4555. PMC 328652. PMID 1886779.
  6. ^ "Entrez Gene: TCF12 transcription factor 12 (HTF4, helix-loop-helix transcription factors 4)".
  7. ^ Ganna A, Verweij KJ, Nivard MG, Maier R, Wedow R, Busch AS, et al. (August 2019). "Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior". Science. 365 (6456): eaat7693. doi:10.1126/science.aat7693. PMC 7082777. PMID 31467194.
  8. ^ Sharma VP, Fenwick AL, Brockop MS, McGowan SJ, Goos JA, Hoogeboom AJ, et al. (March 2013). "Mutations in TCF12, encoding basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis". Nature Genetics. 45 (3): 304–7. doi:10.1038/ng.2531. PMC 3647333. PMID 23354436.
  9. ^ Bhandari RK, Sadler-Riggleman I, Clement TM, Skinner MK (2011-05-17). "Basic helix-loop-helix transcription factor TCF21 is a downstream target of the male sex determining gene SRY". PLOS ONE. 6 (5): e19935. Bibcode:2011PLoSO...619935B. doi:10.1371/journal.pone.0019935. PMC 3101584. PMID 21637323.

Further reading

External links

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