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...

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...

Inferred motif from similar protein – High-throughput in vitro [806] HTTAATTA SETBP1 ENSG00000152217 AT hook Likely sequence specific TF according to literature...

KIAA1147 Yeast two-hybrid assays have shown LCHN to physically interact with SETBP1, a protein that contains 3 nuclear localization signals. Despite the lack...

syndrome 180849 CREBBP Sakoda complex 610871 Schinzel–Giedion syndrome 269150 SETBP1 Split-hand/foot malformation 3 246560 Spondyloepiphyseal dysplasia congenita...

with and without cleft palate: MAFB and ABCA4 Schinzel–Giedion syndrome: SETBP1 Fanconi anemia and related disorders: RAD51C Noonan syndrome: NRAS generalized...

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...

gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1". Nature Medicine. 12 (4): 401–9. doi:10.1038/nm1393. PMID 16582916. S2CID 7601162...

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...

translations sought). In 2012 and 2015 Dr. Gambacorti-Passerini discovered SETBP1 and ETNK1 as two novel oncogenes and identified specific mutations of these...

DOT1L EHMT1, EHMT2, EZH1, EZH2 MLL, MLL2, MLL3, MLL4, MLL5 NSD1 PRDM2 SET, SETBP1, SETD1A, SETD1B, SETD2, SETD3, SETD4, SETD5, SETD6, SETD7, SETD8, SETD9...

gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1". Nat. Med. 12 (4): 401–9. doi:10.1038/nm1393. PMID 16582916. S2CID 7601162...

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...

associated with somatic mutations in at least three other genes viz., ASXL1, SETBP1, and STAG2. Independently of GATA2 mutations and the development of GATA2...

III; 609241; NAGA Schinzel–Giedion midface retraction syndrome; 269150; SETBP1 Schizencephaly; 269160; EMX2 Schizophrenia; 181500; DISC2 Schneckenbecken...