Human Gene CTCFL (uc010giw.1)
  Description: Homo sapiens CCCTC-binding factor (zinc finger protein)-like (CTCFL), transcript variant 5, mRNA.
RefSeq Summary (NM_001269043): CCCTC-binding factor (CTCF), an 11-zinc-finger factor involved in gene regulation, utilizes different zinc fingers to bind varying DNA target sites. CTCF forms methylation-sensitive insulators that regulate X-chromosome inactivation. This gene is a paralog of CTCF and appears to be expressed primarily in the cytoplasm of spermatocytes, unlike CTCF which is expressed primarily in the nucleus of somatic cells. CTCF and the protein encoded by this gene are normally expressed in a mutually exclusive pattern that correlates with resetting of methylation marks during male germ cell differentiation. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2012].
Transcript (Including UTRs)
   Position: hg19 chr20:56,071,021-56,100,183 Size: 29,163 Total Exon Count: 12 Strand: -
Coding Region
   Position: hg19 chr20:56,071,306-56,099,261 Size: 27,956 Coding Exon Count: 11 

Page IndexSequence and LinksPrimersGenetic AssociationsMalaCardsCTD
Gene AllelesRNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein StructureOther Species
mRNA DescriptionsOther NamesModel InformationMethods
Data last updated at UCSC: 2013-06-14

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr20:56,071,021-56,100,183)mRNA (may differ from genome)Protein (700 aa)
Gene SorterGenome BrowserOther Species FASTAGene interactionsTable SchemaAlphaFold
BioGPSEnsemblEntrez GeneExonPrimerGeneCardsH-INV
HGNCLynxMalacardsMGIOMIMPubMed
UniProtKBWikipediaBioGrid 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


-  Genetic Association Studies of Complex Diseases and Disorders
  Genetic Association Database (archive): CTCFL
CDC HuGE Published Literature: CTCFL

-  MalaCards Disease Associations
  MalaCards Gene Search: CTCFL
Diseases sorted by gene-association score: spherocytosis, type 4 (5), silver-russell syndrome (2)

-  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.

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 3.55 RPKM in Testis
Total median expression: 3.79 RPKM



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

+  Microarray Expression Data
  Press "+" in the title bar above to open this section.

-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -54.00111-0.486 Picture PostScript Text
3' UTR -65.40285-0.229 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
IPR007087 - Znf_C2H2
IPR015880 - Znf_C2H2-like
IPR013087 - Znf_C2H2/integrase_DNA-bd

Pfam Domains:
PF00096 - Zinc finger, C2H2 type

SCOP Domains:
57667 - C2H2 and C2HC zinc fingers

ModBase Predicted Comparative 3D Structure on A6XGL8
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 orthologNo orthologNo orthologNo orthologNo ortholog
Gene Details     
Gene Sorter     
      
      
      

-  Descriptions from all associated GenBank mRNAs
  DQ778111 - Homo sapiens BORIS transcription factor transcript variant B1 mRNA, complete cds, alternatively spliced.
DQ778110 - Homo sapiens BORIS transcription factor transcript variant C1 mRNA, complete cds, alternatively spliced.
AF336042 - Homo sapiens nuclear DNA binding factor (BORIS) mRNA, complete cds.
BC060763 - Homo sapiens cDNA clone IMAGE:4825782, containing frame-shift errors.
DQ294738 - Homo sapiens BORIS-like protein (CTCFL) mRNA, complete cds, alternatively spliced.
DQ778108 - Homo sapiens BORIS transcription factor transcript variant A1 mRNA, complete cds, alternatively spliced.
DQ778109 - Homo sapiens BORIS transcription factor transcript variant A2 mRNA, complete cds, alternatively spliced.
DQ778112 - Homo sapiens BORIS transcription factor transcript variant A3 mRNA, complete cds, alternatively spliced.
AY071919 - Homo sapiens zinc finger protein CTCF-T mRNA, complete cds.
AK128070 - Homo sapiens cDNA FLJ46191 fis, clone TESTI4005470, highly similar to Transcriptional repressor CTCFL.
BC130486 - Homo sapiens CCCTC-binding factor (zinc finger protein)-like, mRNA (cDNA clone MGC:163358 IMAGE:40146517), complete cds.
AK313990 - Homo sapiens cDNA, FLJ94642, highly similar to Homo sapiens CCCTC-binding factor (zinc finger protein)-like (CTCFL), mRNA.
KJ900198 - Synthetic construct Homo sapiens clone ccsbBroadEn_09592 CTCFL gene, encodes complete protein.
DQ778115 - Homo sapiens BORIS transcription factor transcript variant C3 mRNA, complete cds, alternatively spliced.
DQ778116 - Homo sapiens BORIS transcription factor transcript variant C4 mRNA, complete cds, alternatively spliced.
DQ778117 - Homo sapiens BORIS transcription factor transcript variant C5 mRNA, complete cds, alternatively spliced.
DQ778118 - Homo sapiens BORIS transcription factor transcript variant C8 mRNA, complete cds, alternatively spliced.
DQ778124 - Homo sapiens BORIS transcription factor transcript variant B2 mRNA, complete cds, alternatively spliced.
DQ778125 - Homo sapiens BORIS transcription factor transcript variant B3 mRNA, complete cds, alternatively spliced.
DQ778121 - Homo sapiens BORIS transcription factor transcript variant C6 mRNA, complete cds, alternatively spliced.
DQ778126 - Homo sapiens BORIS transcription factor transcript variant B4 mRNA, complete cds, alternatively spliced.
DQ778127 - Homo sapiens BORIS transcription factor transcript variant B5 mRNA, complete cds, alternatively spliced.
DQ778122 - Homo sapiens BORIS transcription factor transcript variant A5 mRNA, complete cds, alternatively spliced.
DQ778123 - Homo sapiens BORIS transcription factor transcript variant A6 mRNA, complete cds, alternatively spliced.
DQ778119 - Homo sapiens BORIS transcription factor transcript variant C7 mRNA, complete cds, alternatively spliced.
DQ778120 - Homo sapiens BORIS transcription factor transcript variant C9 mRNA, complete cds, alternatively spliced.
DQ778128 - Homo sapiens BORIS transcription factor transcript variant B6 mRNA, complete cds, alternatively spliced.
DQ778129 - Homo sapiens BORIS transcription factor transcript variant B7 mRNA, complete cds, alternatively spliced.
DQ778114 - Homo sapiens BORIS transcription factor transcript variant C2 mRNA, complete cds, alternatively spliced.
DQ778113 - Homo sapiens BORIS transcription factor transcript variant A4 mRNA, complete cds, alternatively spliced.
DQ778130 - Homo sapiens BORIS transcription factor transcript variant F6 mRNA, partial cds, alternatively spliced.
DQ778131 - Homo sapiens BORIS transcription factor transcript variant F7 mRNA, partial cds, alternatively spliced.
JD019459 - Sequence 483 from Patent EP1572962.
JD029479 - Sequence 10503 from Patent EP1572962.
JD019480 - Sequence 504 from Patent EP1572962.
JD034073 - Sequence 15097 from Patent EP1572962.

-  Other Names for This Gene
  Alternate Gene Symbols: A6XGL8, A6XGL8_HUMAN, NM_001269043, NP_001255972
UCSC ID: uc010giw.1
RefSeq Accession: NM_001269043
Protein: A6XGL8 CCDS: CCDS58780.1

-  Gene Model Information
 
category: coding nonsense-mediated-decay: no RNA accession: NM_001269043.1
exon count: 12CDS single in 3' UTR: no RNA size: 2499
ORF size: 2103CDS single in intron: no Alignment % ID: 100.00
txCdsPredict score: 4405.00frame 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.