Gene Gene information from NCBI Gene database.
Entrez ID 2313
Gene name Fli-1 proto-oncogene, ETS transcription factor
Gene symbol FLI1
Synonyms (NCBI Gene)
BDPLT21EWSR2FLI-1SIC-1
Chromosome 11
Chromosome location 11q24.3
Summary This gene encodes a transcription factor containing an ETS DNA-binding domain. The gene can undergo a t(11;22)(q24;q12) translocation with the Ewing sarcoma gene on chromosome 22, which results in a fusion gene that is present in the majority of Ewing sar
SNPs SNP information provided by dbSNP.
7
SNP ID Visualize variation Clinical significance Consequence
rs773148506 C>A,T Pathogenic Missense variant, coding sequence variant, synonymous variant
rs1064797083 C>T Likely-pathogenic Missense variant, coding sequence variant
rs1064797084 A>G Pathogenic Missense variant, coding sequence variant
rs1064797085 ATTA>- Pathogenic, likely-pathogenic Coding sequence variant, frameshift variant
rs1064797086 G>A Pathogenic, likely-pathogenic Missense variant, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
81
miRTarBase ID miRNA Experiments Reference
MIRT004496 hsa-miR-145-5p qRT-PCRLuciferase reporter assayWestern blot 20382729
MIRT005349 hsa-miR-155-5p Western blot 18950466
MIRT004496 hsa-miR-145-5p Luciferase reporter assayNorthern blotqRT-PCRWestern blot 20737575
MIRT004496 hsa-miR-145-5p Luciferase reporter assayNorthern blotqRT-PCRWestern blot 20737575
MIRT004496 hsa-miR-145-5p Luciferase reporter assayWestern blot 21217773
Transcription factors Transcription factors information provided by TRRUST V2 database.
6
Transcription factor Regulation Reference
ELF1 Activation 19829305
ETS1 Activation 19829305
ETS2 Activation 19829305
FLI1 Activation 19829305
GATA1 Unknown 10523830
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
34
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 IEA
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 ISA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
193067 3749 ENSG00000151702
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q01543
Protein name Friend leukemia integration 1 transcription factor (Proto-oncogene Fli-1) (Transcription factor ERGB)
Protein function Sequence-specific transcriptional activator (PubMed:24100448, PubMed:26316623, PubMed:28255014). Recognizes the DNA sequence 5'-C[CA]GGAAGT-3'.
PDB 1FLI , 1X66 , 2YTU , 5E8G , 5E8I , 5JVT , 6VG2 , 6VG8 , 6VGD , 9CP6 , 9MWY , 9MX8 , 9MX9 , 9MXA
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02198 SAM_PNT 114 198 Sterile alpha motif (SAM)/Pointed domain Domain
PF00178 Ets 282 361 Ets-domain Domain
Sequence
MDGTIKEALSVVSDDQSLFDSAYGAAAHLPKADMTASGSPDYGQPHKINPLPPQQEWINQ
PVRVNVKREYDHMNGSRESPVDCSVSKCSKLVGGGESNPMNYNSYMDEKNGPPPPNMTTN
ERRVIVPADPTLWTQEHVRQWLEWAIKEYSLMEIDTSFFQNMDGKELCKMNKEDFLRATT
LYNTEVLLSHLSYLRESS
LLAYNTTSHTDQSSRLSVKEDPSYDSVRRGAWGNNMNSGLNK
SPPLGGAQTISKNTEQRPQPDPYQILGPTSSRLANPGSGQIQLWQFLLELLSDSANASCI
TWEGTNGEFKMTDPDEVARRWGERKSKPNMNYDKLSRALRYYYDKNIMTKVHGKRYAYKF
D
FHGIAQALQPHPTESSMYKYPSDISYMPSYHAHQQKVNFVPPHPSSMPVTSSSFFGAAS
QYWTSPTGGIYPNPNVPRHPNTHVPSHLGSYY
Sequence length 452
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG 
  Transcriptional misregulation in cancer  
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
28
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession Evidence Score
Abnormal bleeding Likely pathogenic; Pathogenic rs1064797085 RCV001270513
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Bleeding disorder platelet type macrothrombocytopenia Pathogenic rs773148506 RCV000197145
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Bleeding disorder, platelet-type, 21 Likely pathogenic; Pathogenic rs2135925063, rs1131691896, rs2497517912, rs773148506, rs1064797083, rs1064797085, rs1064797087 RCV002245373
RCV002245427
RCV002281010
RCV000487463
RCV000487466
View all (2 more)
★★★★★
ClinVar: Pathogenic / Likely Pathogenic (≥5 Variants)
Thrombocytopenia Likely pathogenic; Pathogenic rs1064797085 RCV001003905
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
11q partial monosomy syndrome Conflicting classifications of pathogenicity ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
AUTOIMMUNE THROMBOCYTOPENIC PURPURA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BLOOD PLATELET DISORDERS Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Cervical cancer Likely benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations