Human Gene TCF23 (uc010ylg.2)
  Description: Homo sapiens transcription factor 23 (TCF23), mRNA.
RefSeq Summary (NM_175769): The gene encodes a member of the basic helix-loop-helix transcription factor family. Studies of the orthologous gene in mouse have shown the encoded protein does not bind DNA but may negatively regulate other basic helix-loop-helix factors via the formation of a functionally inactive heterodimeric complex. [provided by RefSeq, May 2010].
Transcript (Including UTRs)
   Position: hg19 chr2:27,371,945-27,375,819 Size: 3,875 Total Exon Count: 3 Strand: +
Coding Region
   Position: hg19 chr2:27,372,002-27,375,735 Size: 3,734 Coding Exon Count: 3 

Page IndexSequence and LinksUniProtKB CommentsPrimersCTDGene Alleles
RNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein StructureOther SpeciesGO Annotations
mRNA DescriptionsOther NamesModel InformationMethods
Data last updated at UCSC: 2013-06-14

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr2:27,371,945-27,375,819)mRNA (may differ from genome)Protein (214 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
AlphaFoldBioGPSEnsemblEntrez GeneExonPrimerGeneCards
GeneNetworkHGNCHPRDLynxMGIneXtProt
OMIMPubMedTreefamUniProtKBBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: TCF23_HUMAN
DESCRIPTION: RecName: Full=Transcription factor 23; Short=TCF-23; AltName: Full=Class A basic helix-loop-helix protein 24; Short=bHLHa24;
FUNCTION: Inhibits E-box-mediated binding and transactivation of bHLH factors. Inhibitory effect is similar to that of ID proteins. Inhibits the formation of TCF3 and MYOD1 homodimers and heterodimers. Lacks DNA binding activity. Seems to play a role in the inhibition of myogenesis (By similarity).
SUBUNIT: Forms inactive heterodimeric complexes with TCF3 (By similarity).
SUBCELLULAR LOCATION: Nucleus (By similarity).
TISSUE SPECIFICITY: Expressed in liver, kidney and spleen.
DOMAIN: Both the bHLH region and the C-terminal portion are essential for inhibitory function (By similarity).
SIMILARITY: Contains 1 bHLH (basic helix-loop-helix) domain.

-  Primer design for this transcript
 

Primer3Plus can design qPCR Primers that straddle exon-exon-junctions, which amplify only cDNA, not genomic DNA.
Click here to load the transcript sequence and exon structure into Primer3Plus

Exonprimer can design one pair of Sanger sequencing primers around every exon, located in non-genic sequence.
Click here to open Exonprimer with this transcript

To design primers for a non-coding sequence, zoom to a region of interest and select from the drop-down menu: View > In External Tools > Primer3


-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene           more ... click here to view the complete list

+  Common Gene Haplotype Alleles
  Press "+" in the title bar above to open this section.

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 22.46 RPKM in Uterus
Total median expression: 51.24 RPKM



View in GTEx track of Genome Browser    View at GTEx portal     View GTEx Body Map

+  Microarray Expression Data
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-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -22.3057-0.391 Picture PostScript Text
3' UTR -15.4484-0.184 Picture PostScript Text

The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.

-  Protein Domain and Structure Information
  InterPro Domains: Graphical view of domain structure
IPR011598 - HLH_dom

Pfam Domains:
PF00010 - Helix-loop-helix DNA-binding domain

SCOP Domains:
47459 - HLH, helix-loop-helix DNA-binding domain

ModBase Predicted Comparative 3D Structure on Q7RTU1
FrontTopSide
The pictures above may be empty if there is no ModBase structure for the protein. The ModBase structure frequently covers just a fragment of the protein. You may be asked to log onto ModBase the first time you click on the pictures. It is simplest after logging in to just click on the picture again to get to the specific info on that model.

-  Orthologous Genes in Other Species
  Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
MouseRatZebrafishD. melanogasterC. elegansS. cerevisiae
No orthologNo orthologGenome BrowserNo orthologNo orthologNo ortholog
Gene Details     
Gene Sorter     
  Ensembl   
  Protein Sequence   
  Alignment   

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0000981 RNA polymerase II transcription factor activity, sequence-specific DNA binding
GO:0046983 protein dimerization activity

Biological Process:
GO:0006357 regulation of transcription from RNA polymerase II promoter
GO:0007275 multicellular organism development
GO:0007517 muscle organ development
GO:0010628 positive regulation of gene expression
GO:0030154 cell differentiation
GO:0046697 decidualization

Cellular Component:
GO:0005634 nucleus


-  Descriptions from all associated GenBank mRNAs
  BC137191 - Homo sapiens transcription factor 23, mRNA (cDNA clone MGC:168811 IMAGE:9021188), complete cds.
BC137192 - Homo sapiens transcription factor 23, mRNA (cDNA clone MGC:168812 IMAGE:9021189), complete cds.
BC144525 - Homo sapiens cDNA clone IMAGE:9053052.
KJ895650 - Synthetic construct Homo sapiens clone ccsbBroadEn_05044 TCF23 gene, encodes complete protein.

-  Other Names for This Gene
  Alternate Gene Symbols: B2RNZ3, BHLHA24, NM_175769, NP_786951, Q7RTU1, TCF23_HUMAN
UCSC ID: uc010ylg.2
RefSeq Accession: NM_175769
Protein: Q7RTU1 (aka TCF23_HUMAN)
CCDS: CCDS33163.1

-  Gene Model Information
 
category: coding nonsense-mediated-decay: no RNA accession: NM_175769.2
exon count: 3CDS single in 3' UTR: no RNA size: 786
ORF size: 645CDS single in intron: no Alignment % ID: 100.00
txCdsPredict score: 1490.00frame shift in genome: no % Coverage: 100.00
has start codon: yes stop codon in genome: no # of Alignments: 1
has end codon: yes retained intron: no # AT/AC introns 0
selenocysteine: no end bleed into intron: 0# strange splices: 0
Click here for a detailed description of the fields of the table above.

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.