POMT1

gene product
LGMD2K
The protein encoded by this gene is an O-mannosyltransferase that requires interaction with the product of the POMT2 gene for enzymatic function. The encoded protein is found in the membrane of the endoplasmic reticulum. Defects in this gene are a cause of Walker-Warburg syndrome (WWS) and limb-girdle muscular dystrophy type 2K (LGMD2K). Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]
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7 antibodies from 7 providers.

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AntibodyRefsTypeWBELIFIPIHFC
Acris Antibodies GmbH
1 antibody
AP53389PU-NPolyclonal
GeneTex
1 antibody
GTX109717Polyclonal
Novus Biologicals
1 antibody
NBP1-60054Polyclonal
Thermo Fisher Scientific Pierce
1 antibody
PA5-29032Polyclonal
Aviva Systems Biology
1 antibody
ARP44994_P050Polyclonal
LifeSpan BioSciences, Inc.
1 antibody
LS-C102153Polyclonal (Antigen purified)
Sigma-Aldrich
1 antibody
SAB2101845Polyclonal