pathway Info Card

Protein Mannosylation

Information about Protein Mannosylation: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.

Overview of Protein Mannosylation

Most recent studies have shown that Protein Mannosylation shares some biological mechanisms with cell-wall-assembly, cerebral-cortex-development, glycosylation, hypersensitivity, localization, membrane-fusion, pathogenesis, protein-glycosylation, protein-secretion, protein-transport, secretion, transport, vesicle-transport, virulence.

Among the many pathways, these few ones have gauged particular interests from scientists studying Protein Mannosylation, and have been seen in publications frequently: cell-wall-assembly, cerebral-cortex-development, glycosylation, hypersensitivity, localization, membrane-fusion, pathogenesis, protein-glycosylation, protein-secretion, protein-transport, secretion, transport, vesicle-transport, virulence

Quite a number of genes have been found to play important roles in Protein Mannosylation, such as ABCC8, AFM, BAG6, CSH1, DDT, DPM1, ERBB2, EXOSC9, GAS1, GLB1, GOLIM4, NEU1, PDIA6, PSMD3, RPS3, Slc10a5. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.

In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this pathway. Plesae stay updated.

Protein Mannosylation Related Genes

click to see detail information for each gene

ABCC8 AFM BAG6
CSH1 DDT DPM1
ERBB2 EXOSC9 GAS1
GLB1 GOLIM4 NEU1
PDIA6 PSMD3 RPS3
Slc10a5

Diseases Related to Protein Mannosylation

This information is being compiled and will come in a future update

cryptococcal infection infection by cryptococcus neoformans neoplasms
premenstrual tension systemic infection tuberculosis
vitamin a deficiency