Metazoan complexes |
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Details of EWSR1 gene in Homo sapiens
IDs | |||||||||
---|---|---|---|---|---|---|---|---|---|
Link outs | Gene Name | Alias | Uniprot ID | SwissProt ID | NCBI gene ID | ENSEMBL ID | Description | Source | |
| EWSR1 | EWS | Q01844 | EWS_HUMAN | 2130 | ENSG00000182944 | RNA-binding protein EWS | SPROT |
Disease | |||||||||
---|---|---|---|---|---|---|---|---|---|
Disease | OMIM id | ||||||||
Ewing sarcoma (ES) [MIM:612219]: A highly malignant, metastatic, primitive small round cell tumor of bone and soft tissue that affects children and adolescents. It belongs to the Ewing sarcoma family of tumors, a group of morphologically heterogeneous neoplasms that share the same cytogenetic features. They are considered neural tumors derived from cells of the neural crest. Ewing sarcoma represents the less differentiated form of the tumors. Note=The disease is caused by mutations affecting the gene represented in this entry. Chromosomal aberrations involving EWSR1 are found in patients with Ewing sarcoma. Translocation t(1122)(q24q12) with FLI1 translocation t(722)(p22q12) with ETV1 translocation t(2122)(q22q12) with ERG translocation t(922)(q22-31q11-12) with NR4A3. Translocation t(22122)(q23q22q12) that forms a EWSR1-FEV fusion protein with potential oncogenic activity. | 612219 | Note=A chromosomal aberration involving EWSR1 is associated with desmoplastic small round cell tumor (DSRCT). Translocation t(1122)(p13q12) with WT1. | 612219 | Note=A chromosomal aberration involving EWSR1 is associated with malignant melanoma of soft parts (MMSP). Translocation t(1222)(q13q12) with ATF-1. Malignant melanoma of soft parts, also known as soft tissue clear cell sarcoma, is a rare tumor developing in tendons and aponeuroses. | 612219 | Note=A chromosomal aberration involving EWSR1 is associated with small round cell sarcoma. Translocation t(1122)(p36.1q12) with PATZ1. | 612219 | Angiomatoid fibrous histiocytoma (AFH) [MIM:612160]: A distinct variant of malignant fibrous histiocytoma that typically occurs in children and adolescents and is manifest by nodular subcutaneous growth. Characteristic microscopic features include lobulated sheets of histiocyte-like cells intimately associated with areas of hemorrhage and cystic pseudovascular spaces, as well as a striking cuffing of inflammatory cells, mimicking a lymph node metastasis. Note=The disease may be caused by mutations affecting the gene represented in this entry. Chromosomal aberrations involving EWSR1 are found in patients with angiomatoid fibrous histiocytoma. Translocation t(1222)(q13q12) with ATF1 generates a chimeric EWSR1/ATF1 protein. Translocation t(222)(q33q12) with CREB1 generates a EWSR1/CREB1 fusion gene that is most common genetic abnormality in this tumor type. | 612160 | Note=EFPS arise due to chromosomal translocations in which EWSR1 is fused to a variety of cellular transcription factors. EFPS are very potent transcriptional activators dependent on the EAD and a C-terminal DNA-binding domain contributed by the fusion partner. The spectrum of malignancies associated with EFPS are thought to arise via EFP-induced transcriptional deregulation, with the tumor phenotype specified by the EWSR1 fusion partner and cell type. Transcriptional repression of the transforming growth factor beta type II receptor (TGF beta RII) is an important target of the EWS-FLI1, EWS-ERG, or EWS-ETV1 oncogene. | 612160 |
Phenotypes
Abnormality of metabolism/homeostasis, Abnormality of the nervous system, Abnormality of the peripheral nervous system, All, Autosomal dominant inheritance, Mode of inheritance, Neoplasm, Neoplasm by anatomical site, Neoplasm of the nervous system, Neoplasm of the peripheral nervous system, Peripheral neuroepithelioma, Phenotypic abnormality.
Orthologs in other species | |||||||||
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M. musculus | D. melonogaster | C. elegans | S. purpuratus | ||||||
Ewsr1 | caz | fust-1 | Sp-Ewsr1L |
Conserved gene 1 |
Conserved gene 2 |
Conserved score |
H. sapiens gene 1 |
H. sapiens gene 2 |
Complex ID | Corum | BioGrid | IRefWeb | Novelty |
---|---|---|---|---|---|---|---|---|---|
EWSR1 | ECM29 | 0.033787576 | EWSR1 | ECM29 | cpx289 | no | no | no | Novel |
EWSR1 | EIF4H | 0.192578462 | EWSR1 | EIF4H | cpx289 | no | no | no | Novel |
Conserved gene 1 |
Conserved gene 2 |
Conserved score |
H. sapiens gene 1 |
H. sapiens gene 2 |
---|---|---|---|---|
EWSR1 | ACAA2 | 0.100139613 | EWSR1 | ACAA2 |
EWSR1 | HIP1R | 0.073795391 | EWSR1 | HIP1R |
EWSR1 | ACAT1 | 0.086727669 | EWSR1 | ACAT1 |
EWSR1 | POR | 0.094328944 | EWSR1 | POR |
EWSR1 | GORASP2 | 0.076247222 | EWSR1 | GORASP2 |
EWSR1 | PICALM | 0.084271076 | EWSR1 | PICALM |
ANXA2 | EWSR1 | 0.098140039 | ANXA2 | EWSR1 |