Human Gene FOXR1 (uc001pui.3)
  Description: Homo sapiens forkhead box R1 (FOXR1), mRNA.
RefSeq Summary (NM_181721): This gene encodes a member of the forkhead box (FOX) family of transcription factors. FOX family members are monomeric, helix-turn-helix proteins with a core DNA-binding domain of approximately 110 aa. Many FOX transcription factors play roles in determining cell fates during early development. This forkhead box protein lacks the C-terminal basic region found in many other FOX family members. It is located within the 11q23.3 region which is commonly deleted in neuroblastomas. [provided by RefSeq, Jul 2008].
Transcript (Including UTRs)
   Position: hg19 chr11:118,842,417-118,851,995 Size: 9,579 Total Exon Count: 6 Strand: +
Coding Region
   Position: hg19 chr11:118,842,642-118,851,946 Size: 9,305 Coding Exon Count: 6 

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 (chr11:118,842,417-118,851,995)mRNA (may differ from genome)Protein (292 aa)
Gene SorterGenome BrowserOther Species FASTAGene interactionsTable SchemaAlphaFold
BioGPSEnsemblEntrez GeneExonPrimerGeneCardsGeneNetwork
HGNCHPRDLynxMGIneXtProtOMIM
PubMedTreefamUniProtKBBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: FOXR1_HUMAN
DESCRIPTION: RecName: Full=Forkhead box protein R1; AltName: Full=Forkhead box protein N5;
SUBCELLULAR LOCATION: Nucleus (Probable).
SIMILARITY: Contains 1 fork-head DNA-binding 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

+  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: 4.32 RPKM in Testis
Total median expression: 4.48 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 -83.10225-0.369 Picture PostScript Text
3' UTR -6.4049-0.131 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
IPR001766 - TF_fork_head
IPR011991 - WHTH_trsnscrt_rep_DNA-bd

Pfam Domains:
PF00250 - Forkhead domain

SCOP Domains:
46785 - "Winged helix" DNA-binding domain

ModBase Predicted Comparative 3D Structure on Q6PIV2
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:0003677 DNA binding
GO:0003700 transcription factor activity, sequence-specific DNA binding
GO:0005515 protein binding
GO:0043565 sequence-specific DNA binding

Biological Process:
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
GO:0006357 regulation of transcription from RNA polymerase II promoter
GO:0009653 anatomical structure morphogenesis
GO:0030154 cell differentiation

Cellular Component:
GO:0005634 nucleus


-  Descriptions from all associated GenBank mRNAs
  AB094092 - Homo sapiens DLNB13 mRNA, complete cds.
BC028191 - Homo sapiens forkhead box R1, mRNA (cDNA clone MGC:40176 IMAGE:5167039), complete cds.
BC125040 - Homo sapiens forkhead box R1, mRNA (cDNA clone MGC:149486 IMAGE:40115641), complete cds.
BC038969 - Homo sapiens forkhead box R1, mRNA (cDNA clone MGC:47864 IMAGE:5164198), complete cds.
JD522219 - Sequence 503243 from Patent EP1572962.
JD165015 - Sequence 146039 from Patent EP1572962.
JD124855 - Sequence 105879 from Patent EP1572962.
KJ906474 - Synthetic construct Homo sapiens clone ccsbBroadEn_16144 FOXR1 gene, encodes complete protein.
KJ895954 - Synthetic construct Homo sapiens clone ccsbBroadEn_05348 FOXR1 gene, encodes complete protein.
KJ904390 - Synthetic construct Homo sapiens clone ccsbBroadEn_13784 hypothetical protein, encodes complete protein.
BC064340 - Homo sapiens cDNA clone IMAGE:4369995, **** WARNING: chimeric clone ****.

-  Other Names for This Gene
  Alternate Gene Symbols: B0YJ15, DLNB13, FOXN5, FOXR1_HUMAN, NM_181721, NP_859072, Q6PIV2, Q86UT9, Q8IXX2
UCSC ID: uc001pui.3
RefSeq Accession: NM_181721
Protein: Q6PIV2 (aka FOXR1_HUMAN)
CCDS: CCDS31688.1

-  Gene Model Information
 
category: coding nonsense-mediated-decay: no RNA accession: NM_181721.2
exon count: 6CDS single in 3' UTR: no RNA size: 1215
ORF size: 879CDS single in intron: no Alignment % ID: 100.00
txCdsPredict score: 1890.00frame shift in genome: no % Coverage: 94.90
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.