FGFR1OP Back

FGFR1 oncogene partner

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NCBI Description of FGFR1OP
This gene encodes a largely hydrophilic protein postulated to be a leucine-rich protein family member. A t(6;8)(q27;p11) chromosomal translocation, fusing this gene and the fibroblast growth factor receptor 1 (FGFR1) gene, has been found in cases of myeloproliferative disorder. The resulting chimeric protein contains the N-terminal leucine-rich region of this encoded protein fused to the catalytic domain of FGFR1. This gene is thought to play an important role in normal proliferation and differentiation of the erythroid lineage. Alternatively spliced transcript variants that encode different proteins have been identified.

Community Annotation of FGFR1OP Add / Edit FGFR1OP: Annotations

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Figure notes


• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


Legend

FGFR1OP is highly significantly mutated in
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FGFR1OP is significantly mutated in
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FGFR1OP is near significance in
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Click on a tumor type to see its full list of significant genes.

Data details


• Mutation list for FGFR1OP