PP3958 [Homo sapiens]

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A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If). [J Clin Invest. 2001]
A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If).
Kranz C, Denecke J, Lehrman MA, Ray S, Kienz P, Kreissel G, Sagi D, Peter-Katalinic J, Freeze HH, Schmid T, et al. J Clin Invest. 2001 Dec; 108(11):1613-9.
MPDU1 regulates CEACAM1 and cell adhesion in vitro and in vivo. [Glycoconj J. 2018]
MPDU1 regulates CEACAM1 and cell adhesion in vitro and in vivo.
Bennett DC, Cazet A, Charest J, Contessa JN. Glycoconj J. 2018 Jun; 35(3):265-274. Epub 2018 Apr 18.
Expression cloning of a novel suppressor of the Lec15 and Lec35 glycosylation mutations of Chinese hamster ovary cells. [J Biol Chem. 1996]
Expression cloning of a novel suppressor of the Lec15 and Lec35 glycosylation mutations of Chinese hamster ovary cells.
Ware FE, Lehrman MA. J Biol Chem. 1996 Jun 14; 271(24):13935-8.

RefSeq genomic sequence
See the genomic reference sequence for the MPDU1 gene (NG_009204.1).
RefSeq protein isoforms
See 6 reference sequence protein isoforms for the MPDU1 gene.

PP3958 [Homo sapiens]
PP3958 [Homo sapiens]
gi|10834682|gb|AAG23771.1|AF258568_

Protein
Immunoelectrophoresis
Immunoelectrophoresis
A technique that combines protein electrophoresis and double immunodiffusion. In this procedure proteins are first separated by gel electrophoresis (usually agarose), then mad...<br/>

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Protein