RecName: Full=Dolichol-phosphate mannosyltransferase subunit 1; AltNam - Protein

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A new intronic mutation in the DPM1 gene is associated with a milder form of CDG Ie in two French siblings. [Pediatr Res. 2006]
A new intronic mutation in the DPM1 gene is associated with a milder form of CDG Ie in two French siblings.
Dancourt J, Vuillaumier-Barrot S, de Baulny HO, Sfaello I, Barnier A, le Bizec C, Dupre T, Durand G, Seta N, Moore SE. Pediatr Res. 2006 Jun; 59(6):835-9. Epub 2006 Apr 26.
Congenital disorder of glycosylation (CDG) type Ie. A new patient. [J Inherit Metab Dis. 2004]
Congenital disorder of glycosylation (CDG) type Ie. A new patient.
García-Silva MT, Matthijs G, Schollen E, Cabrera JC, Sanchez del Pozo J, Martí Herreros M, Simón R, Maties M, Martín Hernández E, Hennet T, et al. J Inherit Metab Dis. 2004; 27(5):591-600.
Deficiency of dolichol-phosphate-mannose synthase-1 causes congenital disorder of glycosylation type Ie. [J Clin Invest. 2000]
Deficiency of dolichol-phosphate-mannose synthase-1 causes congenital disorder of glycosylation type Ie.
Imbach T, Schenk B, Schollen E, Burda P, Stutz A, Grunewald S, Bailie NM, King MD, Jaeken J, Matthijs G, et al. J Clin Invest. 2000 Jan; 105(2):233-9.

RefSeq genomic sequence
See the genomic reference sequence for the DPM1 gene (NG_008923.1).
RefSeq protein isoforms
See 6 reference sequence protein isoforms for the DPM1 gene.

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O60762 [Domain Mapping of Disease Mut...]
O60762
Domain Mapping of Disease Mutations
MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF) [MODBASE, Database of Comparat...]
MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF)
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RecName: Full=Dolichol-phosphate mannosyltransferase subunit 1; AltName: Full=Do...
RecName: Full=Dolichol-phosphate mannosyltransferase subunit 1; AltName: Full=Dolichol-phosphate mannose synthase subunit 1; Short=DPM synthase subunit 1; AltName: Full=Dolichyl-phosphate beta-D-mannosyltransferase subunit 1; AltName: Full=Mannose-P-dolichol synthase subunit 1; Short=MPD synthase subunit 1
gi|20137697|sp|O60762.1|DPM1_HUMAN

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