gene 2 or CMG2) is a protein that in humans is encoded by the ANTXR2 gene. Mutations in ANTXR2 are associated with infantile systemic hyalinosis and juvenile...
10 KB (1,282 words) - 22:00, 6 March 2024
contractures.: 606 This disease is caused by mutations in the CMG2 gene (ANTXR2). Skin lesion List of cutaneous conditions James, William; Berger, Timothy;...
2 KB (118 words) - 22:15, 17 April 2024
HGNC:500 P15144 772 ANTKMT HGNC:14152 Q9BQD7 773 ANTXR1 HGNC:21014 Q9H6X2 774 ANTXR2 HGNC:21732 P58335 775 ANTXRL HGNC:27277 A6NF34 776 ANXA1 HGNC:533 P04083...
277 KB (17 words) - 23:17, 27 April 2024
of the structures of PA, EF, LF, and the cellular receptors (ANTXR1 and ANTXR2). Structures for the toxin molecules (Figs. 3–5), the receptor, and the...
26 KB (3,581 words) - 15:17, 20 July 2024
manner in which the metal ion is coordinated differs slightly. ANTXR1; ANTXR2; BF; C2; CACHD1; CACNA2D1; CACNA2D2; CACNA2D3; CACNA2D4; CFB; CLCA1; CLCA2;...
8 KB (791 words) - 11:13, 28 March 2024
hypotonia. This condition is due to mutations in the anthrax toxin receptor-2 (ANTXR2) gene. This gene is also known as capillary morphogenesis protein-2. This...
5 KB (443 words) - 09:45, 20 August 2024
Fibromatosis, gingival, 2; 135300; GINGF2 Fibromatosis, juvenile hyaline; 228600; ANTXR2 Fibrosis of extraocular muscles, congenital, 1; 135700; KIF21A Fibrosis...
234 KB (18,877 words) - 15:43, 9 May 2024