Mannosyltransferases

"Mannosyltransferases" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

Enzymes that catalyze the transfer of mannose from a nucleoside diphosphate mannose to an acceptor molecule which is frequently another carbohydrate. The group includes EC 2.4.1.32, EC 2.4.1.48, EC 2.4.1.54, and EC 2.4.1.57.

Descriptor ID

D008364

MeSH Number(s)

D08.811.913.400.450.560

Concept/Terms

Mannosyltransferases

Below are MeSH descriptors whose meaning is more general than "Mannosyltransferases".

Chemicals and Drugs [D]
Enzymes and Coenzymes [D08]
Enzymes [D08.811]
Transferases [D08.811.913]
Glycosyltransferases [D08.811.913.400]
Hexosyltransferases [D08.811.913.400.450]
Mannosyltransferases [D08.811.913.400.450.560]

Below are MeSH descriptors whose meaning is related to "Mannosyltransferases".

Below are MeSH descriptors whose meaning is more specific than "Mannosyltransferases".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Mannosyltransferases" by people in Harvard Catalyst Profiles by year, and whether "Mannosyltransferases" was a major or minor topic of these publication.

Bar chart showing 19 publications over 12 distinct years, with a maximum of 3 publications in 2012

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
1999	1	0	1
2001	1	0	1
2002	2	0	2
2005	2	0	2
2012	1	2	3
2015	1	0	1
2016	1	0	1
2017	1	1	2
2018	1	0	1
2019	1	1	2
2020	0	2	2
2022	1	0	1

Below are the most recent publications written about "Mannosyltransferases" by people in Profiles.

A genome-wide CRISPR screen identifies DPM1 as a modifier of DPAGT1 deficiency and ER stress. PLoS Genet. 2022 09; 18(9):e1010430.

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Neuroimaging manifestations and genetic heterogeneity of Walker-Warburg syndrome in Saudi patients. Brain Dev. 2021 Mar; 43(3):380-388.

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A defect in GPI synthesis as a suggested mechanism for the role of ARV1 in intellectual disability and seizures. Neurogenetics. 2020 10; 21(4):259-267.

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Mutations in PIGB Cause an Inherited GPI Biosynthesis Defect with an Axonal Neuropathy and Metabolic Abnormality in Severe Cases. Am J Hum Genet. 2019 08 01; 105(2):384-394.

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Mycobacterium smegmatis HtrA Blocks the Toxic Activity of a Putative Cell Wall Amidase. Cell Rep. 2019 05 21; 27(8):2468-2479.e3.

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PiggyBac-based screening identified BEM4 as a suppressor to rescue growth defects in och1-disrupted yeast cells. Biosci Biotechnol Biochem. 2018 Sep; 82(9):1497-1507.

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Limb girdle muscular dystrophy due to mutations in POMT2. J Neurol Neurosurg Psychiatry. 2018 05; 89(5):506-512.

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Cystic kidneys in fetal Walker-Warburg syndrome with POMT2 mutation: Intrafamilial phenotypic variability in four siblings and review of literature. Am J Med Genet A. 2017 Oct; 173(10):2697-2702.

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Congenital disorders of glycosylation: The Saudi experience. Am J Med Genet A. 2017 Oct; 173(10):2614-2621.

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ALG1-CDG: Clinical and Molecular Characterization of 39 Unreported Patients. Hum Mutat. 2016 07; 37(7):653-60.

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