Gene Gene information from NCBI Gene database.
Entrez ID 2119
Gene name ETS variant transcription factor 5
Gene symbol ETV5
Synonyms (NCBI Gene)
ERM
Chromosome 3
Chromosome location 3q27.2
miRNA miRNA information provided by mirtarbase database.
250
miRTarBase ID miRNA Experiments Reference
MIRT017311 hsa-miR-335-5p Microarray 18185580
MIRT530651 hsa-miR-4453 PAR-CLIP 22012620
MIRT530650 hsa-miR-4538 PAR-CLIP 22012620
MIRT530649 hsa-miR-1539 PAR-CLIP 22012620
MIRT530648 hsa-miR-5689 PAR-CLIP 22012620
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
37
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IDA 17126306
GO:0000785 Component Chromatin ISA
GO:0000976 Function Transcription cis-regulatory region binding IDA 19443906
GO:0000977 Function RNA polymerase II transcription regulatory region sequence-specific DNA binding IMP 15857832
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
601600 3494 ENSG00000244405
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P41161
Protein name ETS translocation variant 5 (Ets-related protein ERM)
Protein function Binds to DNA sequences containing the consensus nucleotide core sequence 5'-GGAA.-3'.
PDB 4UNO , 5ILV
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04621 ETS_PEA3_N 1 366 PEA3 subfamily ETS-domain transcription factor N terminal domain Family
PF00178 Ets 369 448 Ets-domain Domain
Tissue specificity TISSUE SPECIFICITY: Ubiquitous.
Sequence
Sequence length 510
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG 
  Transcriptional misregulation in cancer
Prostate cancer
 
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
4
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Myoepithelial tumor Pathogenic rs772183700 RCV002463939
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
ETV5-related disorder Likely benign rs151057501, rs2473932174, rs200588942 RCV003912042
RCV003942066
RCV003969240
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma Associate 35396535
Adenocarcinoma of Lung Associate 31503425
Airway Remodeling Associate 31443657
Azoospermia Nonobstructive Associate 22771031
Bipolar Disorder Associate 31754094
Breast Neoplasms Associate 34224831, 35317849
Carcinogenesis Associate 24756106
Carcinoma Endometrioid Associate 24756106
Carcinoma Intraductal Noninfiltrating Associate 31162284
Carcinoma Ovarian Epithelial Associate 22589409