dolichyl-phosphate mannosyltransferase polypeptide 3, also known as DPM3, is a human gene. Dolichol-phosphate mannose (Dol-P-Man) serves as a donor of...
4 KB (537 words) - 12:37, 19 January 2024
Lehle L, Wevers RA (July 2009). "Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies"...
41 KB (3,730 words) - 21:20, 22 June 2024
HGNC:25199 Q9BTV6 4499 DPM1 HGNC:3005 O60762 4500 DPM2 HGNC:3006 O94777 4501 DPM3 HGNC:3007 Q9P2X0 4502 DPP3 HGNC:3008 Q9NY33 4503 DPP4 HGNC:3009 P27487 4504...
277 KB (17 words) - 23:17, 27 April 2024
dolichol-phosphate-mannose synthase consists of three subunits, DPM1, DPM2 and DPM3". EMBO J. 19 (11): 2475–82. doi:10.1093/emboj/19.11.2475. PMC 212771. PMID 10835346...
4 KB (546 words) - 21:20, 29 January 2023
interactions between FAM117A1 and these other human proteins: Aquaporin-6 Caspase 6 DPM3 ELOVL4 FATE1 JAGN1 LAMP2 PBX3 SGPL1 SH3GLB1 TMX2 GRCh38: Ensembl release...
3 KB (308 words) - 13:57, 29 July 2023
well. Abnormal flexibility might occur, spinal curvature possible. CDG I (DPM3) some of the symptoms at birth and throughout the infant's life are weakness...
33 KB (3,529 words) - 15:22, 12 July 2024
dolichol-phosphate-mannose synthase consists of three subunits, DPM1, DPM2 and DPM3". The EMBO Journal. 19 (11): 2475–82. doi:10.1093/emboj/19.11.2475. PMC 212771...
6 KB (724 words) - 22:12, 10 December 2023
In; 612015; RFT1 Congenital disorder of glycosylation, type Io; 612937; DPM3 Congenital disorder of glycosylation, type Ip; 612379; SRD5A3 Congenital...
234 KB (18,877 words) - 15:43, 9 May 2024