exchange factor FGD1 (Rho/Rac GEF) is a protein that in humans is encoded by the FGD1 gene that lies on the X chromosome. Orthologs of the FGD1 gene are found...
13 KB (1,607 words) - 23:01, 27 July 2024
has been reported. Mutations in the FGD1 gene are the only known genetic cause of Aarskog-Scott syndrome. The FGD1 gene provides instructions for making...
9 KB (874 words) - 19:51, 23 August 2024
syndrome) AAAS recessive 1:1,000,000 Aarskog–Scott syndrome FGD1 X-linked recessive 1:25,000 ABCD syndrome EDNRB recessive 1:18,000-20,000...
42 KB (983 words) - 10:34, 21 August 2024
"Crystal structures of F420-dependent glucose-6-phosphate dehydrogenase FGD1 involved in the activation of the anti-tuberculosis drug candidate PA-824...
23 KB (2,413 words) - 18:07, 8 June 2024
Aarskog–Scott syndrome: a survey of the clinical variability in light of FGD1 mutation analysis in 46 patients". European Journal of Human Genetics. 12...
9 KB (1,043 words) - 19:16, 2 June 2024
FYVE, RhoGEF and PH domain containing (FGD) is a gene family consisting of: FGD1 FGD2 FGD3 FGD4 Type 1 is associated with Aarskog-Scott syndrome. Guanine...
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HGNC:19061 Q5NUL3 5623 FGA HGNC:3661 P02671 5624 FGB HGNC:3662 P02675 5625 FGD1 HGNC:3663 P98174 5626 FGD2 HGNC:3664 Q7Z6J4 5627 FGD3 HGNC:16027 Q5JSP0 5628...
277 KB (17 words) - 15:46, 9 May 2024
DOK3, DOK4, DOK5, DOK6, DTGCU2, EXOC8, FAM109A, FAM109B, FARP1, FARP2, FGD1, FGD2, FGD3, FGD4, FGD5, FGD6, GAB1, GAB2, GAB3, GAB4, GRB10, GRB14, GRB7...
14 KB (1,434 words) - 15:11, 10 June 2024
several different causes which define the type.[citation needed] FGD type 1 (FGD1 or GCCD1) is caused by mutations in the ACTH receptor (melanocortin 2 receptor;...
4 KB (376 words) - 10:21, 5 March 2024
glucose-6-phosphate dehydrogenase, F420-dependent glucose-6-phosphate dehydrogenase, FGD1, Rv0407, F420-dependent glucose-6-phosphate dehydrogenase 1) is an enzyme...
2 KB (227 words) - 14:15, 26 August 2023