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| General information | Expression | Regulation | Mutation | Interaction |
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Basic Information |
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Gene ID | 222235 |
Name | FBXL13 |
Synonymous | Fbl13;F-box and leucine-rich repeat protein 13;FBXL13;F-box and leucine-rich repeat protein 13 |
Definition | F-box/LRR-repeat protein 13 |
Position | 7q22.1 |
Gene type | protein-coding |
Source | Count: 2; TAG,Generif |
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Sentence |
Abstract |
| "We have extensively characterized the FBXL13, NAPE-PLD, and SVH genes as candidate myeloid tumor suppressors." | Monosomy 7 and deletions of 7q are recurring leukemia-associated cytogenetic abnormalities that correlate with adverse outcomes in children and adults. We describe a 2.52-Mb genomic DNA contig that spans a commonly deleted segment of chromosome band 7q22 identified in myeloid malignancies. This interval currently includes 14 genes, 19 predicted genes, and 5 predicted pseudogenes. We have extensively characterized the FBXL13, NAPE-PLD, and SVH genes as candidate myeloid tumor suppressors. FBXL13 encodes a novel F-box protein, SVHis a member of a gene family that contains Armadillo-like repeats, and NAPE-PLD encodes a phospholipase D-type phosphodiesterase. Analysis of a panel of leukemia specimens with monosomy 7 did not reveal mutations in these or in the candidate genes LRRC17, PRO1598, and SRPK2. This fully sequenced and annotated contig provides a resource for candidate myeloid tumor suppressor gene discovery. |
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