FK506-binding protein 10 is a protein that in humans is encoded by the FKBP10 gene. The protein encoded by this gene belongs to the FKBP-type peptidyl-prolyl...
5 KB (482 words) - 20:34, 13 October 2022
types. Bruck syndrome type 1 is caused by a homozygous mutation in the FKBP10 gene. Type 2 is caused by a homozygous mutation in the PLOD2 gene. Type...
8 KB (781 words) - 19:32, 8 May 2024
SERPINH1 gene on chromosome 11q13. Type XI – OI caused by mutations in FKBP10 on chromosome 17q21. The mutations cause a decrease in secretion of trimeric...
150 KB (15,385 words) - 00:51, 15 October 2024
Category:EC 5.2 FKBP: FKBP1A FKBP1B FKBP2 FKBP3 FKBP4 FKBP5 FKBP6 FKBP8 FKBP9 FKBP10 FKBPL Cyclophilin Parvulin Prolyl isomerase 2-chloro-4-carboxymethylenebut-2-en-1...
33 KB (3,650 words) - 18:48, 10 September 2024
HGNC:3723 Q9Y680 5705 FKBP8 HGNC:3724 Q14318 5706 FKBP9 HGNC:3725 O95302 5707 FKBP10 HGNC:18169 Q96AY3 5708 FKBP11 HGNC:18624 Q9NYL4 5709 FKBP14 HGNC:18625 Q9NWM8...
277 KB (17 words) - 18:41, 6 October 2024
FKBP1A; FKBP1B; FKBP2; FKBP3; FKBP4; FKBP5; FKBP6; FKBP7; FKBP8; FKBP9; FKBP10; FKBP11; FKBP14; FKBP15; Gene with unclear status (may be pseudogene): FKBP1C...
6 KB (656 words) - 18:45, 22 August 2023
EFCBP1; EFCBP2; EFHA1; EFHA2; EFHB; EFHC1; EFHD1; EFHD2; EPS15; EPS15L1 FKBP10; FKBP14; FKBP7; FKBP9; FKBP9L; FREQ; FSTL1; FSTL5 GCA; GPD2; GUCA1A; GUCA1B;...
17 KB (2,077 words) - 16:17, 5 September 2024
imperfecta, type IX; 259440; PPIB Osteogenesis imperfecta, type VI; 610698; FKBP10 Osteogenesis imperfecta, type VII; 610682; CRTAP Osteogenesis imperfecta...
234 KB (18,877 words) - 15:43, 9 May 2024