Homo sapiens Protein: ETV6 | |||||||||||||||||||||||
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Summary | |||||||||||||||||||||||
InnateDB Protein | IDBP-237652.7 | ||||||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||||||
Gene Symbol | ETV6 | ||||||||||||||||||||||
Protein Name | ets variant 6 | ||||||||||||||||||||||
Synonyms | TEL; TEL/ABL; | ||||||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||||||
Ensembl Protein | ENSP00000379658 | ||||||||||||||||||||||
InnateDB Gene | IDBG-19967 (ETV6) | ||||||||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||||||||
Function | Transcriptional repressor; binds to the DNA sequence 5'- CCGGAAGT-3'. | ||||||||||||||||||||||
Subcellular Localization | Nucleus. | ||||||||||||||||||||||
Disease Associations | Note=A chromosomal aberration involving ETV6 is found in a form of chronic myelomonocytic leukemia (CMML). Translocation t(5;12)(q33;p13) with PDGFRB. It is characterized by abnormal clonal myeloid proliferation and by progression to acute myelogenous leukemia (AML).Note=Chromosomal aberrations involving ETV6 are found in a form of acute myeloid leukemia (AML). Translocation t(12;22)(p13;q11) with MN1; translocation t(4;12)(q12;p13) with CHIC2.Note=Chromosomal aberrations involving ETV6 are found in childhood acute lymphoblastic leukemia (ALL). Translocations t(12;21)(p12;q22) and t(12;21)(p13;q22) with RUNX1/AML1.Note=A chromosomal aberration involving ETV6 is found in a form of pre-B acute myeloid leukemia. Translocation t(9;12)(p24;p13) with JAK2.Note=A chromosomal aberration involving ETV6 is found in myelodysplastic syndrome (MDS) with basophilia. Translocation t(5;12)(q31;p13) with ACSL6.Note=A chromosomal aberration involving ETV6 is found in acute eosinophilic leukemia (AEL). Translocation t(5;12)(q31;p13) with ACSL6.Note=A chromosomal aberration involving ETV6 is found in myelodysplastic syndrome (MDS). Translocation t(1;12)(p36.1;p13) with MDS2.Myeloproliferative disorder chronic with eosinophilia (MPE) [MIM:131440]: A hematologic disorder characterized by malignant eosinophils proliferation. Note=The gene represented in this entry is involved in disease pathogenesis. A chromosomal aberration involving ETV6 is found in many instances of myeloproliferative disorder chronic with eosinophilia. Translocation t(5;12) with PDGFRB on chromosome 5 creating an ETV6-PDGFRB fusion protein.Leukemia, acute myelogenous (AML) [MIM:601626]: A subtype of acute leukemia, a cancer of the white blood cells. AML is a malignant disease of bone marrow characterized by maturational arrest of hematopoietic precursors at an early stage of development. Clonal expansion of myeloid blasts occurs in bone marrow, blood, and other tissue. Myelogenous leukemias develop from changes in cells that normally produce neutrophils, basophils, eosinophils and monocytes. {ECO:0000269PubMed:15806161}. Note=The gene represented in this entry is involved in disease pathogenesis.Note=A chromosomal aberration involving ETV6 is found in acute lymphoblastic leukemia. Translocation t(9;12)(p13;p13) with PAX5. | ||||||||||||||||||||||
Tissue Specificity | Ubiquitous. | ||||||||||||||||||||||
Comments | |||||||||||||||||||||||
Interactions | |||||||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 43 experimentally validated interaction(s) in this database.
They are also associated with 15 interaction(s) predicted by orthology.
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Gene Ontology | |||||||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||||||||
PDB ID | |||||||||||||||||||||||
InterPro |
IPR000418
Ets domain IPR003118 Pointed domain IPR013761 Sterile alpha motif/pointed domain |
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PFAM |
PF00178
PF02198 |
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PRINTS |
PR00454
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PIRSF | |||||||||||||||||||||||
SMART |
SM00413
SM00251 |
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TIGRFAMs | |||||||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||||||
Modification | |||||||||||||||||||||||
Cross-References | |||||||||||||||||||||||
SwissProt | P41212 | ||||||||||||||||||||||
PhosphoSite | PhosphoSite-P41212 | ||||||||||||||||||||||
TrEMBL | Q9UME7 | ||||||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||||||
Entrez Gene | 2120 | ||||||||||||||||||||||
UniGene | Hs.504765 | ||||||||||||||||||||||
RefSeq | NP_001978 | ||||||||||||||||||||||
HUGO | HGNC:3495 | ||||||||||||||||||||||
OMIM | 600618 | ||||||||||||||||||||||
CCDS | CCDS8643 | ||||||||||||||||||||||
HPRD | 15976 | ||||||||||||||||||||||
IMGT | |||||||||||||||||||||||
EMBL | AK289441 BC043399 CH471094 DQ841178 U11732 U61375 U63312 U63313 U81834 | ||||||||||||||||||||||
GenPept | AAA19786 AAB17134 AAB17135 AAB39882 AAC50690 AAH43399 ABI30005 BAF82130 EAW96240 | ||||||||||||||||||||||