Human Gene TCF20 (ENST00000677622.1_9) from GENCODE V47lift37
  Description: transcription factor 20, transcript variant 3 (from RefSeq NM_001378418.1)
Gencode Transcript: ENST00000677622.1_9
Gencode Gene: ENSG00000100207.21_18
Transcript (Including UTRs)
   Position: hg19 chr22:42,556,019-42,666,659 Size: 110,641 Total Exon Count: 6 Strand: -
Coding Region
   Position: hg19 chr22:42,564,659-42,611,311 Size: 46,653 Coding Exon Count: 4 

Page IndexSequence and LinksPrimersMalaCardsCTDGene Alleles
Microarray ExpressionRNA StructureOther SpeciesmRNA DescriptionsOther NamesModel Information
Methods
Data last updated at UCSC: 2024-08-22 23:36:26

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr22:42,556,019-42,666,659)mRNA (may differ from genome)Protein (1960 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
AlphaFoldBioGPSEnsemblEntrez GeneExonPrimerGeneCards
HGNCMalacardsMGIOMIMPubMedUniProtKB
WikipediaBioGrid CRISPR DB

-  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


-  MalaCards Disease Associations
  MalaCards Gene Search: TCF20
Diseases sorted by gene-association score: vertebrobasilar insufficiency (11), breast sarcoma (11), leukoencephalopathy with vanishing white matter (6), autism spectrum disorder (1)

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene

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

+  Microarray Expression Data
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-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -191.70351-0.546 Picture PostScript Text
3' UTR -413.101390-0.297 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.

-  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 orthologNo orthologNo orthologNo orthologNo ortholog
Gene DetailsGene Details    
Gene SorterGene Sorter    
 RGD    
      
      

-  Descriptions from all associated GenBank mRNAs
  BC156502 - Synthetic construct Homo sapiens clone IMAGE:100063133, MGC:190700 transcription factor 20 (AR1) (TCF20) mRNA, encodes complete protein.
AB006630 - Homo sapiens mRNA for KIAA0292 gene, partial cds.
LP895442 - Sequence 306 from Patent EP3253886.
U19345 - Homo sapiens AR1 (TCF20) mRNA, partial cds.
BC172542 - Synthetic construct Homo sapiens clone IMAGE:100069236, MGC:199247 transcription factor 20 (AR1) (TCF20) mRNA, encodes complete protein.
KF851355 - Homo sapiens transcription factor 20 (TCF20) mRNA, complete cds.
AB527391 - Synthetic construct DNA, clone: pF1KA0292, Homo sapiens TCF20 gene for transcription factor 20, without stop codon, in Flexi system.
BC013180 - Homo sapiens transcription factor 20 (AR1), mRNA (cDNA clone IMAGE:4340825), with apparent retained intron.
JD532747 - Sequence 513771 from Patent EP1572962.
JD475452 - Sequence 456476 from Patent EP1572962.
JD078621 - Sequence 59645 from Patent EP1572962.
JD532855 - Sequence 513879 from Patent EP1572962.
JD546166 - Sequence 527190 from Patent EP1572962.
JD092671 - Sequence 73695 from Patent EP1572962.
JD433595 - Sequence 414619 from Patent EP1572962.
JD312339 - Sequence 293363 from Patent EP1572962.
JD207883 - Sequence 188907 from Patent EP1572962.
JD552442 - Sequence 533466 from Patent EP1572962.
JD140237 - Sequence 121261 from Patent EP1572962.
JD125019 - Sequence 106043 from Patent EP1572962.
JD191219 - Sequence 172243 from Patent EP1572962.
JD396758 - Sequence 377782 from Patent EP1572962.
JD276878 - Sequence 257902 from Patent EP1572962.
DQ570918 - Homo sapiens piRNA piR-31030, complete sequence.

-  Other Names for This Gene
  Alternate Gene Symbols: hCG_41553 , NM_001378418, TCF20 , uc330cwh.1, uc330cwh.2, W5ZR30, W5ZR30_HUMAN
UCSC ID: ENST00000677622.1_9
RefSeq Accession: NM_001378418.1

-  Gene Model Information
  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.