ETV2 (ETS variant transcription factor 2) - Rat Genome Database
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Gene: ETV2 (ETS variant transcription factor 2) Homo sapiens
Analyze
Symbol: ETV2
Name: ETS variant transcription factor 2
RGD ID: 1351650
HGNC Page HGNC
Description: Exhibits sequence-specific double-stranded DNA binding activity. Predicted to be involved in several processes, including in utero embryonic development; mesoderm formation; and regulation of gene expression. Predicted to localize to nucleus; INTERACTS WITH 5-fluorouracil; benzo[a]pyrene; bisphenol A.
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: ER71; ETS translocation variant 2; ETS variant 2; ets variant gene 2; ets-related protein 71; ETSRP71; MGC129834; MGC129835
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1935,641,745 - 35,644,871 (+)EnsemblGRCh38hg38GRCh38
GRCh381935,641,175 - 35,644,871 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371936,132,647 - 36,135,773 (+)NCBIGRCh37GRCh37hg19GRCh37
GRCh371936,132,647 - 36,136,007 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361940,824,487 - 40,827,613 (+)NCBINCBI36hg18NCBI36
Celera1932,846,129 - 32,849,256 (+)NCBI
Cytogenetic Map19q13.12NCBI
HuRef1932,637,910 - 32,641,036 (+)NCBIHuRef
CHM1_11936,134,171 - 36,137,305 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View
dystonia  (IAGP)

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
nucleus  (IBA,IEA)

References

References - curated
1. GOA_HUMAN data from the GO Consortium
2. RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:1340465   PMID:12087183   PMID:12477932   PMID:14702039   PMID:15057824   PMID:16344560   PMID:16619273   PMID:18270322   PMID:19274049   PMID:21873635   PMID:25540418   PMID:27488544  
PMID:28003219   PMID:28026128   PMID:28473536   PMID:29697486   PMID:30021884   PMID:31432499   PMID:31534512   PMID:31744543  


Genomics

Comparative Map Data
ETV2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1935,641,745 - 35,644,871 (+)EnsemblGRCh38hg38GRCh38
GRCh381935,641,175 - 35,644,871 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371936,132,647 - 36,135,773 (+)NCBIGRCh37GRCh37hg19GRCh37
GRCh371936,132,647 - 36,136,007 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361940,824,487 - 40,827,613 (+)NCBINCBI36hg18NCBI36
Celera1932,846,129 - 32,849,256 (+)NCBI
Cytogenetic Map19q13.12NCBI
HuRef1932,637,910 - 32,641,036 (+)NCBIHuRef
CHM1_11936,134,171 - 36,137,305 (+)NCBICHM1_1
Etv2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39730,333,041 - 30,335,934 (-)NCBIGRCm39mm39
GRCm38730,633,616 - 30,636,509 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl730,633,616 - 30,635,852 (-)EnsemblGRCm38mm10GRCm38
MGSCv37731,418,635 - 31,420,871 (-)NCBIGRCm37mm9NCBIm37
MGSCv36730,342,378 - 30,344,612 (-)NCBImm8
Celera725,225,816 - 25,227,677 (-)NCBICelera
Cytogenetic Map7B1NCBI
Etv2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.2185,890,562 - 85,894,025 (-)NCBI
Rnor_6.0 Ensembl189,091,239 - 89,094,530 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.0189,091,239 - 89,094,570 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.0190,246,861 - 90,250,074 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4185,684,698 - 85,686,914 (-)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.1185,762,809 - 85,765,732 (-)NCBI
Celera180,262,333 - 80,264,853 (-)NCBICelera
Cytogenetic Map1q21NCBI
Etv2
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554684,857,595 - 4,860,531 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554684,857,023 - 4,859,926 (+)NCBIChiLan1.0ChiLan1.0
ETV2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.11941,307,864 - 41,311,004 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1941,307,864 - 41,311,004 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v01932,571,829 - 32,575,083 (+)NCBIMhudiblu_PPA_v0panPan3
ETV2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1 Ensembl1116,971,365 - 116,985,796 (-)EnsemblCanFam3.1canFam3CanFam3.1
CanFam3.11116,971,238 - 116,974,831 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Etv2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
SpeTri2.0NW_004936570671,152 - 673,768 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ETV2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl645,088,171 - 45,089,595 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1645,085,984 - 45,089,592 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2640,543,308 - 40,546,424 (+)NCBISscrofa10.2Sscrofa10.2susScr3
ETV2
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1630,552,780 - 30,556,374 (+)NCBI
ChlSab1.1 Ensembl630,553,931 - 30,556,355 (+)Ensembl
Etv2
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046247947,985,662 - 7,989,063 (-)NCBI

Position Markers
RH98938  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map19q13.12UniSTS
GeneMap99-GB4 RH Map19215.84UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1649
Count of miRNA genes:426
Interacting mature miRNAs:456
Transcripts:ENST00000379023, ENST00000379026, ENST00000402764, ENST00000403402, ENST00000479824, ENST00000591135
Prediction methods:Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system adipose tissue appendage entire extraembryonic component
High
Medium 2 2 1 2 354
Low 1677 1212 1600 537 1096 396 3061 500 1531 327 1052 1458 151 1087 1565
Below cutoff 754 1755 122 83 823 66 1206 1599 2171 88 45 150 19 117 1135 4

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001300974 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001304549 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_014209 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005258652 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011526624 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017026472 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA885210 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC002115 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF000671 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK097439 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC040908 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC107123 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC107124 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC140746 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC144448 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB046527 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HY053182 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JC009158 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JC261284 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000379023   ⟹   ENSP00000368309
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1935,641,745 - 35,644,871 (+)Ensembl
RefSeq Acc Id: ENST00000379026   ⟹   ENSP00000368312
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1935,641,745 - 35,644,871 (+)Ensembl
RefSeq Acc Id: ENST00000402764   ⟹   ENSP00000384524
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1935,641,745 - 35,644,871 (+)Ensembl
RefSeq Acc Id: ENST00000403402   ⟹   ENSP00000385369
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1935,642,155 - 35,644,852 (+)Ensembl
RefSeq Acc Id: ENST00000479824   ⟹   ENSP00000468453
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1935,641,793 - 35,644,871 (+)Ensembl
RefSeq Acc Id: ENST00000591135   ⟹   ENSP00000475089
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1935,643,666 - 35,644,682 (+)Ensembl
RefSeq Acc Id: ENST00000619399   ⟹   ENSP00000477924
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1935,641,745 - 35,643,745 (+)Ensembl
RefSeq Acc Id: ENST00000621247   ⟹   ENSP00000480641
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1935,642,139 - 35,644,871 (+)Ensembl
RefSeq Acc Id: NM_001300974   ⟹   NP_001287903
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381935,641,745 - 35,644,871 (+)NCBI
CHM1_11936,134,171 - 36,137,305 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001304549   ⟹   NP_001291478
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381935,641,745 - 35,644,871 (+)NCBI
CHM1_11936,134,171 - 36,137,305 (+)NCBI
Sequence:
RefSeq Acc Id: NM_014209   ⟹   NP_055024
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381935,641,745 - 35,644,871 (+)NCBI
GRCh371936,132,647 - 36,136,007 (+)NCBI
Build 361940,824,487 - 40,827,613 (+)NCBI Archive
Celera1932,846,129 - 32,849,256 (+)RGD
HuRef1932,637,910 - 32,641,036 (+)RGD
CHM1_11936,134,171 - 36,137,305 (+)NCBI
Sequence:
RefSeq Acc Id: XM_005258652   ⟹   XP_005258709
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381935,641,757 - 35,644,871 (+)NCBI
GRCh371936,132,647 - 36,136,007 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011526624   ⟹   XP_011524926
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381935,641,175 - 35,644,871 (+)NCBI
Sequence:
RefSeq Acc Id: XM_017026472   ⟹   XP_016881961
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381935,641,757 - 35,644,871 (+)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_055024   ⟸   NM_014209
- Peptide Label: isoform 1
- UniProtKB: O00321 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_005258709   ⟸   XM_005258652
- Peptide Label: isoform X1
- UniProtKB: O00321 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001291478   ⟸   NM_001304549
- Peptide Label: isoform 3
- UniProtKB: Q3KNT2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001287903   ⟸   NM_001300974
- Peptide Label: isoform 2
- UniProtKB: K7ERX2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011524926   ⟸   XM_011526624
- Peptide Label: isoform X3
- UniProtKB: K7ERX2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016881961   ⟸   XM_017026472
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: ENSP00000480641   ⟸   ENST00000621247
RefSeq Acc Id: ENSP00000468453   ⟸   ENST00000479824
RefSeq Acc Id: ENSP00000384524   ⟸   ENST00000402764
RefSeq Acc Id: ENSP00000385369   ⟸   ENST00000403402
RefSeq Acc Id: ENSP00000368312   ⟸   ENST00000379026
RefSeq Acc Id: ENSP00000368309   ⟸   ENST00000379023
RefSeq Acc Id: ENSP00000477924   ⟸   ENST00000619399
RefSeq Acc Id: ENSP00000475089   ⟸   ENST00000591135
Protein Domains
ETS

Promoters
RGD ID:7239547
Promoter ID:EPDNEW_H25520
Type:initiation region
Name:ETV2_1
Description:ETS variant 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381935,641,745 - 35,641,805EPDNEW
RGD ID:6795430
Promoter ID:HG_KWN:29668
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   Lymphoblastoid
Transcripts:ENST00000222279,   ENST00000379021,   ENST00000379023,   ENST00000379026,   ENST00000402764,   ENST00000403402,   NM_014209,   OTTHUMT00000318846,   UC002OAT.2
Position:
Human AssemblyChrPosition (strand)Source
Build 361940,824,154 - 40,824,654 (+)MPROMDB
RGD ID:6815240
Promoter ID:HG_MRA:8042
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:AF000671
Position:
Human AssemblyChrPosition (strand)Source
Build 361940,825,596 - 40,826,352 (+)MPROMDB
RGD ID:6816223
Promoter ID:HG_SPT:30721
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:AA885210,   AW170266,   DB336666,   DB337633
Position:
Human AssemblyChrPosition (strand)Source
Build 361940,827,156 - 40,827,656 (-)MPROMDB

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3 copy number gain See cases [RCV000133888] Chr19:11227942..44626354 [GRCh38]
Chr19:11338618..45129651 [GRCh37]
Chr19:11199618..49821491 [NCBI36]
Chr19:19p13.2-q13.31		 pathogenic
GRCh38/hg38 19q12-13.13(chr19:29661858-38114723)x1 copy number loss See cases [RCV000135879] Chr19:29661858..38114723 [GRCh38]
Chr19:30152765..38605363 [GRCh37]
Chr19:34844605..43297203 [NCBI36]
Chr19:19q12-13.13		 pathogenic
GRCh38/hg38 19q12-13.13(chr19:29671324-37902990)x1 copy number loss See cases [RCV000136794] Chr19:29671324..37902990 [GRCh38]
Chr19:30162231..38393630 [GRCh37]
Chr19:34854071..43085470 [NCBI36]
Chr19:19q12-13.13		 pathogenic
GRCh37/hg19 19q13.12(chr19:35658728-36173537)x3 copy number gain not provided [RCV000752672] Chr19:35658728..36173537 [GRCh37]
Chr19:19q13.12		 benign
GRCh37/hg19 19q13.12(chr19:35723176-36183886)x3 copy number gain See cases [RCV000448697] Chr19:35723176..36183886 [GRCh37]
Chr19:19q13.12		 uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3 copy number gain See cases [RCV000511289] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic|uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888) copy number gain See cases [RCV000512296] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3 copy number gain not provided [RCV000752439] Chr19:68029..59110290 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3 copy number gain not provided [RCV000752444] Chr19:260912..59097160 [GRCh37]
Chr19:19p13.3-q13.43		 pathogenic
GRCh37/hg19 19q13.11-13.12(chr19:35111811-37744992) copy number loss Generalized epilepsy with febrile seizures plus, type 1 [RCV000767768] Chr19:35111811..37744992 [GRCh37]
Chr19:19q13.11-13.12		 pathogenic
GRCh37/hg19 19q13.11-13.12(chr19:35043556-36316644) copy number loss not provided [RCV000767769] Chr19:35043556..36316644 [GRCh37]
Chr19:19q13.11-13.12		 pathogenic
GRCh37/hg19 19q11-13.33(chr19:28271106-49213832)x3 copy number gain not provided [RCV000845733] Chr19:28271106..49213832 [GRCh37]
Chr19:19q11-13.33		 pathogenic
GRCh37/hg19 19q13.12(chr19:35613953-36183886)x1 copy number loss not provided [RCV000845987] Chr19:35613953..36183886 [GRCh37]
Chr19:19q13.12		 uncertain significance
Single allele deletion Dystonia [RCV001003865] Chr19:35553425..36264299 [GRCh37]
Chr19:19q13.12		 pathogenic

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:3491 AgrOrtholog
COSMIC ETV2 COSMIC
Ensembl Genes ENSG00000105672 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000368309 ENTREZGENE, UniProtKB/TrEMBL
  ENSP00000368312 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000384524 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000385369 UniProtKB/Swiss-Prot
  ENSP00000468453 ENTREZGENE, UniProtKB/TrEMBL
  ENSP00000475089 UniProtKB/TrEMBL
  ENSP00000477924 UniProtKB/TrEMBL
  ENSP00000480641 UniProtKB/TrEMBL
Ensembl Transcript ENST00000379023 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000379026 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000402764 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000403402 UniProtKB/Swiss-Prot
  ENST00000479824 ENTREZGENE, UniProtKB/TrEMBL
  ENST00000591135 UniProtKB/TrEMBL
  ENST00000619399 UniProtKB/TrEMBL
  ENST00000621247 UniProtKB/TrEMBL
Gene3D-CATH 1.10.10.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000105672 GTEx
HGNC ID HGNC:3491 ENTREZGENE
Human Proteome Map ETV2 Human Proteome Map
InterPro Ets_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WH-like_DNA-bd_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  WH_DNA-bd_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:2116 UniProtKB/Swiss-Prot
NCBI Gene 2116 ENTREZGENE
OMIM 609358 OMIM
Pfam Ets UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA27905 PharmGKB
PRINTS ETSDOMAIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE ETS_DOMAIN_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ETS_DOMAIN_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ETS_DOMAIN_3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART ETS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF46785 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A087WTJ5_HUMAN UniProtKB/TrEMBL
  A0A087WX03_HUMAN UniProtKB/TrEMBL
  B7ZMD4_HUMAN UniProtKB/TrEMBL
  ETV2_HUMAN UniProtKB/Swiss-Prot
  K7ERX2 ENTREZGENE, UniProtKB/TrEMBL
  O00321 ENTREZGENE
  Q3KNT2 ENTREZGENE, UniProtKB/TrEMBL
  Q3KNT3_HUMAN UniProtKB/TrEMBL
  S4R454_HUMAN UniProtKB/TrEMBL
UniProt Secondary A6NFN5 UniProtKB/Swiss-Prot
  B3KUL0 UniProtKB/Swiss-Prot
  B9EIN1 UniProtKB/Swiss-Prot
  Q9UEA0 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2019-09-12 ETV2  ETS variant transcription factor 2  ETV2  ETS variant 2  Symbol and/or name change 5135510 APPROVED
2016-02-29 ETV2  ETS variant 2    ets variant 2  Symbol and/or name change 5135510 APPROVED