SET binding protein 1 is a protein that in humans is encoded by the SETBP1 gene. The gene is located on Chromosome 18, specifically on the long (q) arm...
10 KB (1,419 words) - 02:44, 29 November 2023
the parents. It is caused by a new spontaneous mutation of the SETBP1 gene. The SETBP1 gene is a cancer promoting gene, and affected children who survive...
6 KB (470 words) - 15:09, 27 October 2023
with and without cleft palate: MAFB and ABCA4 Schinzel–Giedion syndrome: SETBP1 Fanconi anemia and related disorders: RAD51C Noonan syndrome: NRAS generalized...
2 KB (172 words) - 22:38, 16 June 2019
Inferred motif from similar protein – High-throughput in vitro [806] HTTAATTA SETBP1 ENSG00000152217 AT hook Likely sequence specific TF according to literature...
374 KB (81 words) - 02:10, 23 September 2023
translations sought). In 2012 and 2015 Dr. Gambacorti-Passerini discovered SETBP1 and ETNK1 as two novel oncogenes and identified specific mutations of these...
6 KB (634 words) - 04:55, 28 May 2024
P58005 14608 SESTD1 HGNC:18379 Q86VW0 14609 SET HGNC:10760 Q01105 14610 SETBP1 HGNC:15573 Q9Y6X0 14611 SETD1A HGNC:29010 O15047 14612 SETD1B HGNC:29187...
282 KB (17 words) - 09:00, 31 May 2024
specific inhibitor of the BCR-ABL protein and in particular for CML. In 2012 SETBP1 was identified as a novel oncogene in aCML; specific somatic mutations of...
8 KB (721 words) - 21:56, 8 January 2024
syndrome 180849 CREBBP Sakoda complex 610871 Schinzel–Giedion syndrome 269150 SETBP1 Split-hand/foot malformation 3 246560 Spondyloepiphyseal dysplasia congenita...
35 KB (2,495 words) - 01:53, 15 June 2024
gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1". Nature Medicine. 12 (4): 401–409. doi:10.1038/nm1393. PMID 16582916. S2CID 7601162...
173 KB (17,853 words) - 05:36, 9 June 2024