Homeobox protein SIX5 is a protein that in humans is encoded by the SIX5 gene. GRCh38: Ensembl release 89: ENSG00000177045 – Ensembl, May 2017 GRCm38:...
5 KB (589 words) - 17:51, 4 January 2024
cause of branchio-oto-renal syndrome are mutations in genes, EYA1, SIX1, and SIX5 (approximately 40 percent of those born with this condition have a mutation...
13 KB (1,179 words) - 06:19, 1 May 2024
LASS6; HNF-class: HMBOX1; HNF1A, HNF1B; SINE-class: SIX1, SIX2, SIX3, SIX4, SIX5, SIX6 CUT-class: ONECUT1, ONECUT2, ONECUT3; CUX1, CUX2; SATB1, SATB2; ZF-class:...
41 KB (4,385 words) - 21:28, 21 August 2024
ENSG00000100625 Homeodomain Known motif – High-throughput in vitro [818] VBGTATCRB SIX5 ENSG00000177045 Homeodomain Known motif – In vivo/Misc source [819] GGAGTTGT...
374 KB (81 words) - 02:10, 23 September 2023
HGNC:10888 Q9NPC8 14824 SIX3 HGNC:10889 O95343 14825 SIX4 HGNC:10890 Q9UIU6 14826 SIX5 HGNC:10891 Q8N196 14827 SIX6 HGNC:10892 O95475 14828 SKA1 HGNC:28109 Q96BD8...
282 KB (17 words) - 18:42, 6 October 2024
Branchiooculofacial syndrome; 113620; TFAP2A Branchiootorenal syndrome 2; 610896; SIX5 Branchiootorenal syndrome with cataract; 113650; EYA1 Branchiootorenal syndrome;...
234 KB (18,877 words) - 06:16, 6 November 2024
expansion on chromatin structure and expression of DMPK and neighboring genes, SIX5 and DMWD, in myotonic dystrophy". Mol. Genet. Metab. 74 (1–2): 281–91. doi:10...
5 KB (587 words) - 04:24, 27 May 2024