Human Gene ETV1 (uc022aac.1)
  Description: Homo sapiens ets variant 1 (ETV1), transcript variant 4, mRNA.
RefSeq Summary (NM_001163149): This gene encodes a member of the ETS (E twenty-six) family of transcription factors. The ETS proteins regulate many target genes that modulate biological processes like cell growth, angiogenesis, migration, proliferation and differentiation. All ETS proteins contain an ETS DNA-binding domain that binds to DNA sequences containing the consensus 5'-CGGA[AT]-3'. The protein encoded by this gene contains a conserved short acidic transactivation domain (TAD) in the N-terminal region, in addition to the ETS DNA-binding domain in the C-terminal region. This gene is involved in chromosomal translocations, which result in multiple fusion proteins including EWS-ETV1 in Ewing sarcoma and at least 10 ETV1 partners (see PMID: 19657377, Table 1) in prostate cancer. In addition to chromosomal rearrangement, this gene is overexpressed in prostate cancer, melanoma and gastrointestinal stromal tumor. Multiple alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2016].
Transcript (Including UTRs)
   Position: hg19 chr7:13,930,856-14,030,865 Size: 100,010 Total Exon Count: 12 Strand: -
Coding Region
   Position: hg19 chr7:13,946,138-14,028,677 Size: 82,540 Coding Exon Count: 9 

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 (chr7:13,930,856-14,030,865)mRNA (may differ from genome)Protein (459 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
AlphaFoldBioGPSEnsemblEntrez GeneExonPrimerGeneCards
HGNCHuman Cortex Gene ExpressionLynxMalacardsMGIOMIM
PubMedUniProtKBWikipediaBioGrid 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): ETV1
CDC HuGE Published Literature: ETV1
Positive Disease Associations: Audiometry, Pure-Tone , Iron , Thyrotropin
Related Studies:
  1. Audiometry, Pure-Tone
    , , . [PubMed 0]
  2. Iron
    , , . [PubMed 0]
  3. Thyrotropin
    Shih-Jen Hwang et al. BMC medical genetics 2007, A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study., BMC medical genetics. [PubMed 17903292]
    Kidney function traits and TSH are associated with SNPs on the Affymetrix GeneChip Human Mapping 100K SNP set. These data will serve as a valuable resource for replication as more SNPs associated with kidney function and endocrine traits are identified.
           more ... click here to view the complete list

-  MalaCards Disease Associations
  MalaCards Gene Search: ETV1
Diseases sorted by gene-association score: ewing sarcoma* (233), gastrointestinal stromal tumor (13), microphthalmia, isolated 1 (5), prostate cancer (5), male reproductive organ cancer (1)
* = Manually curated disease association

-  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: 74.35 RPKM in Brain - Cerebellar Hemisphere
Total median expression: 223.51 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 -57.46206-0.279 Picture PostScript Text
3' UTR -1272.185042-0.252 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
  Pfam Domains:
PF00178 - Ets-domain
PF04621 - PEA3 subfamily ETS-domain transcription factor N terminal domain

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

ModBase Predicted Comparative 3D Structure on P50549-2
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 orthologGenome BrowserNo orthologNo orthologNo orthologNo ortholog
 Gene Details    
 Gene Sorter    
 RGD    
 Protein Sequence    
 Alignment    

-  Descriptions from all associated GenBank mRNAs
  AB209202 - Homo sapiens mRNA for ets variant gene 1 variant protein.
BC098403 - Homo sapiens ets variant 1, mRNA (cDNA clone MGC:104699 IMAGE:30345383), complete cds.
CR627389 - Homo sapiens mRNA; cDNA DKFZp781L0674 (from clone DKFZp781L0674).
AK299693 - Homo sapiens cDNA FLJ50641 complete cds, highly similar to ETS translocation variant 1.
BC106762 - Homo sapiens ets variant 1, mRNA (cDNA clone MGC:120533 IMAGE:40025690), complete cds.
BC106763 - Homo sapiens ets variant 1, mRNA (cDNA clone MGC:120534 IMAGE:40025693), complete cds.
U17163 - Human transcription factor ETV1 mRNA, complete cds.
AK294572 - Homo sapiens cDNA FLJ50494 complete cds, highly similar to ETS translocation variant 1.
AK294755 - Homo sapiens cDNA FLJ51675 complete cds, highly similar to ETS translocation variant 1.
AK293802 - Homo sapiens cDNA FLJ50459 complete cds, highly similar to ETS translocation variant 1.
BC045776 - Homo sapiens ets variant 1, mRNA (cDNA clone IMAGE:5259971), with apparent retained intron.
AK316007 - Homo sapiens cDNA, FLJ78906 complete cds, highly similar to ETS translocation variant 1.
X87175 - H.sapiens mRNA for ER81 transcription factor.
AK312863 - Homo sapiens cDNA, FLJ93307, highly similar to Homo sapiens ets variant gene 1 (ETV1), mRNA.
EU446473 - Synthetic construct Homo sapiens clone IMAGE:100070228; IMAGE:100011682; FLH257296.01L ets variant gene 1 (ETV1) gene, encodes complete protein.
KJ891126 - Synthetic construct Homo sapiens clone ccsbBroadEn_00520 ETV1 gene, encodes complete protein.
AB463032 - Synthetic construct DNA, clone: pF1KB3955, Homo sapiens ETV1 gene for ets variant gene 1, without stop codon, in Flexi system.
AK309190 - Homo sapiens cDNA, FLJ99231.
AK311134 - Homo sapiens cDNA, FLJ18176.
AK311194 - Homo sapiens cDNA, FLJ18236.
AK311089 - Homo sapiens cDNA, FLJ18131.
AK311707 - Homo sapiens cDNA, FLJ18749.
EF632110 - Homo sapiens HNRPA2B1/ETV1 fusion transcript mRNA, partial sequence.
LF209519 - JP 2014500723-A/17022: Polycomb-Associated Non-Coding RNAs.
AK055368 - Homo sapiens cDNA FLJ30806 fis, clone FEBRA2001334.
LF329240 - JP 2014500723-A/136743: Polycomb-Associated Non-Coding RNAs.
LF329239 - JP 2014500723-A/136742: Polycomb-Associated Non-Coding RNAs.
BC042950 - Homo sapiens ets variant gene 1, mRNA (cDNA clone IMAGE:5273913).
JD492783 - Sequence 473807 from Patent EP1572962.
JD433233 - Sequence 414257 from Patent EP1572962.
JD305908 - Sequence 286932 from Patent EP1572962.
JD298119 - Sequence 279143 from Patent EP1572962.
AF070641 - Homo sapiens clone 24421 mRNA sequence.
JD349165 - Sequence 330189 from Patent EP1572962.
JD167374 - Sequence 148398 from Patent EP1572962.
JD298951 - Sequence 279975 from Patent EP1572962.
LF209891 - JP 2014500723-A/17394: Polycomb-Associated Non-Coding RNAs.
JD350346 - Sequence 331370 from Patent EP1572962.
JD396438 - Sequence 377462 from Patent EP1572962.
JD350405 - Sequence 331429 from Patent EP1572962.
JD301352 - Sequence 282376 from Patent EP1572962.
JD488690 - Sequence 469714 from Patent EP1572962.
JD310636 - Sequence 291660 from Patent EP1572962.
HM245386 - Homo sapiens KLK2-ETV1 breakpoint junction transcript variant 2 mRNA sequence.
HM245385 - Homo sapiens KLK2-ETV1 breakpoint junction transcript variant 1 mRNA sequence.
MA564817 - JP 2018138019-A/136743: Polycomb-Associated Non-Coding RNAs.
MA564816 - JP 2018138019-A/136742: Polycomb-Associated Non-Coding RNAs.
MA445096 - JP 2018138019-A/17022: Polycomb-Associated Non-Coding RNAs.
MA445468 - JP 2018138019-A/17394: Polycomb-Associated Non-Coding RNAs.
LF332455 - JP 2014500723-A/139958: Polycomb-Associated Non-Coding RNAs.
JD436316 - Sequence 417340 from Patent EP1572962.
MA568032 - JP 2018138019-A/139958: Polycomb-Associated Non-Coding RNAs.

-  Other Names for This Gene
  Alternate Gene Symbols: ER81, NM_001163149, NP_001156621, P50549-2
UCSC ID: uc022aac.1
RefSeq Accession: NM_001163149
Protein: P50549-2, splice isoform of P50549

-  Gene Model Information
 
category: coding nonsense-mediated-decay: yes RNA accession: NM_001163149.1
exon count: 12CDS single in 3' UTR: no RNA size: 6237
ORF size: 972CDS single in intron: no Alignment % ID: 100.00
txCdsPredict score: 1233.50frame shift in genome: no % Coverage: 99.73
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.