Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
2113
Gene name Gene Name - the full gene name approved by the HGNC.
ETS proto-oncogene 1, transcription factor
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ETS1
Synonyms (NCBI Gene) Gene synonyms aliases
ETS-1, EWSR2, c-ets-1, p54
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q24.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the ETS family of transcription factors, which are defined by the presence of a conserved ETS DNA-binding domain that recognizes the core consensus DNA sequence GGAA/T in target genes. These proteins function either as transc
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs1565372210 TCCTTG>AA Pathogenic Coding sequence variant, frameshift variant, intron variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT000641 hsa-miR-9-5p Luciferase reporter assay 19956200
MIRT005104 hsa-miR-155-5p Luciferase reporter assay, qRT-PCR, Western blot 18950466
MIRT005104 hsa-miR-155-5p Luciferase reporter assay, qRT-PCR, Western blot 18950466
MIRT005104 hsa-miR-155-5p Microarray 19193853
MIRT004975 hsa-miR-31-5p Luciferase reporter assay, qRT-PCR 19524507
Transcription factors
Transcription factor Regulation Reference
ETV4 Activation 8247540
ETV7 Unknown 22615925
JUN Activation 1945412
NR3C1 Repression 17016446
RARA Unknown 11327309
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000785 Component Chromatin ISA
GO:0000976 Function Transcription cis-regulatory region binding IDA 31146003
GO:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IDA 12119294
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IBA
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IDA 21711453
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
164720 3488 ENSG00000134954
Protein
UniProt ID P14921
Protein name Protein C-ets-1 (p54)
Protein function Transcription factor (PubMed:10698492, PubMed:11909962). Directly controls the expression of cytokine and chemokine genes in a wide variety of different cellular contexts (PubMed:20378371). May control the differentiation, survival and prolifera
PDB 1GVJ , 2NNY , 2STT , 2STW , 3MFK , 3RI4 , 3WTS , 3WTT , 3WTU , 3WTV , 3WTW , 3WTX , 3WTY , 3WTZ , 3WU0 , 3WU1 , 4L0Y , 4L0Z , 4L18 , 4LG0 , 5ZMC
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02198 SAM_PNT 53 136 Sterile alpha motif (SAM)/Pointed domain Domain
PF00178 Ets 336 415 Ets-domain Domain
Tissue specificity TISSUE SPECIFICITY: Highly expressed within lymphoid cells. Isoforms c-ETS-1A and Ets-1 p27 are both detected in all fetal tissues tested, but vary with tissue type in adult tissues. None is detected in brain or kidney. {ECO:0000269|PubMed:19377509, ECO:0
Sequence
MKAAVDLKPTLTIIKTEKVDLELFPSPDMECADVPLLTPSSKEMMSQALKATFSGFTKEQ
QRLGIPKDPRQWTETHVRDWVMWAVNEFSLKGVDFQKFCMNGAALCALGKDCFLELAPDF
VGDILWEHLEILQKED
VKPYQVNGVNPAYPESRYTSDYFISYGIEHAQCVPPSEFSEPSF
ITESYQTLHPISSEELLSLKYENDYPSVILRDPLQTDTLQNDYFAIKQEVVTPDNMCMGR
TSRGKLGGQDSFESIESYDSCDRLTQSWSSQSSFNSLQRVPSYDSFDSEDYPAALPNHKP
KGTFKDYVRDRADLNKDKPVIPAAALAGYTGSGPIQLWQFLLELLTDKSCQSFISWTGDG
WEFKLSDPDEVARRWGKRKNKPKMNYEKLSRGLRYYYDKNIIHKTAGKRYVYRFV
CDLQS
LLGYTPEELHAMLDVKPDADE
Sequence length 441
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Ras signaling pathway
Cellular senescence
Human T-cell leukemia virus 1 infection
Pathways in cancer
Renal cell carcinoma
  Oncogene Induced Senescence
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Asthma Pediatric asthma, Asthma (childhood onset), Asthma N/A N/A GWAS
Biliary Cholangitis Primary biliary cholangitis N/A N/A GWAS
Celiac disease Celiac disease N/A N/A GWAS
Congenital Heart Disease congenital heart disease N/A N/A GenCC
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Acrospiroma Associate 17785952
Acute Kidney Injury Associate 35611792
Adenocarcinoma Associate 11399944, 12377649, 17785952, 28592290
Adenocarcinoma Stimulate 21892521
Adenocarcinoma Mucinous Associate 8952528
Adenocarcinoma of Lung Associate 17785952, 28617551, 32432746, 35212617, 37545222
Adenoma Associate 21892521
Alzheimer Disease Associate 37100862
Anaphylaxis Associate 34142482
Antiphospholipid Syndrome Associate 30471352