TCF12
TCF12
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TCF12

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TCF12
Available structures
PDBOrtholog search: PDBe RCSB
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
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001253862
NM_001253863
NM_001253864
NM_001253865
NM_011544

RefSeq (protein)

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[3][4]
Wikidata
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Transcription factor 12 is a protein that in humans is encoded by the TCF12 gene.[5][6]

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.[6] TCF12 has been speculatively related to human male sexuality through a GWAS study indicating association to a related single nucleotide polymorphism.[7] Mutations in this gene have also been associated with cases of coronal craniosynostosis.[8]

TCF12 is the primary heterodimerising partner of TCF21, a tumour suppressor gene and a target of SRY/SOX9 activity.[9]

References

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Further reading

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