PHD finger protein 6 is a protein that in humans is encoded by the PHF6 gene. This gene is a member of the plant homeodomain (PHD)-like finger (PHF) family...
10 KB (1,101 words) - 08:57, 27 March 2022
disability. BFLS is an X-linked recessive genetic disease caused by mutations in PHF6, a gene that encodes a zinc finger protein involved in cell growth. Point...
8 KB (716 words) - 16:23, 14 November 2023
six-residue segments, namely PHF6 (VQIVYK) and PHF6* (VQIINK), can form tau PHF aggregation in AD. Apart from the PHF6, some other residue sites like...
56 KB (6,277 words) - 06:22, 26 April 2024
HGNC:8920 O75151 12059 PHF3 HGNC:8921 Q92576 12060 PHF5A HGNC:18000 Q7RTV0 12061 PHF6 HGNC:18145 Q8IWS0 12062 PHF7 HGNC:18458 Q9BWX1 12063 PHF8 HGNC:20672 Q9UPP1...
282 KB (17 words) - 23:17, 27 April 2024
genes mutations associated to this syndrome, including SOX11, ARID2, DPF2, PHF6, SMARCA2, SMARCA4, SMARCB1, SMARCC2, SMARCE1, SOX4. The diagnosis is generally...
8 KB (724 words) - 00:19, 5 February 2024
1038/ng.892. PMC 3297422. PMID 21804550. Van Vlierberghe, P.; et al. (2010). "PHF6 mutations in T-cell acute lymphoblastic leukemia". Nat Genet. 42 (4): 338–342...
13 KB (1,502 words) - 00:33, 15 August 2023
Boomerang dysplasia; 112310; FLNB Börjeson–Forssman–Lehmann syndrome; 301900; PHF6 Bosley–Salih–Alorainy syndrome; 601536; HOXA1 Bothnia retinal dystrophy;...
234 KB (18,877 words) - 15:43, 9 May 2024