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ProteomicsTMEM260 is a protein-specific O-mannosyltransferase
Mutations in the TMEM260 gene cause structural heart defects and renal anomalies syndrome (SHDRA), but the function of the encoded protein remains unknown. We report that TMEM260 is an ER-located protein O-mannosyltransferase that selectively glycosylates defined extracellular immunoglobulin, plexin...
ORGANISM(S): Homo sapiens (Human) Mus musculus (Mouse) 
2023-05-05 | PXD032328 | Pride
O-mannosylation Glycoproteomics Glycopeptide Tmem260 
UnknownMutations in TMEM260 Cause a Pediatric Neurodevelopmental, Cardiac, and Renal Syndrome.
Not available
S-EPMC5384036 | biostudies-literature
UnknownA <i>TMEM260</i> Biallelic Deletion Underlies Truncus Arteriosus.
Not available
S-EPMC12688340 | biostudies-literature
UnknownThe SHDRA syndrome-associated gene <i>TMEM260</i> encodes a protein-specific O-mannosyltransferase.
Not available
S-EPMC10214176 | biostudies-literature
UnknownThe c.1617del variant of TMEM260 is identified as the most frequent single gene determinant for Japanese patients with a specific type of congenital heart disease.
Not available
S-EPMC11043032 | biostudies-literature
UnknownGenetic etiology of truncus arteriosus excluding 22q11.2 deletion syndrome and identification of c.1617del, a prevalent variant in TMEM260, in the Japanese population.
Not available
S-EPMC11043042 | biostudies-literature
ProteomicsGlobal view of domain-specific O-linked mannose glycosylation in glycoengineered cells
Protein O-linked mannose (O-Man) glycosylation is an evolutionary conserved post-translational modification, whose biosynthesis is initiated by three non-redundant enzyme families, POMT1/POMT2, TMTC1-4 and TMEM260. In this study, we applied a targeted workflow for membrane glycoproteomics to five hu...
ORGANISM(S): Homo sapiens (Human) 
2024-06-10 | PXD045597 | Pride
Lc-msms O-man Glycoproteomics Ptm Glycobiology O-mannose 
GenomicsDanio rerio
Danio rerio Raw sequence reads
PRJNA1259525 | ENA
UnknownGlobal View of Domain-Specific O-Linked Mannose Glycosylation in Glycoengineered Cells.
Not available
S-EPMC11292533 | biostudies-literature
UnknownCorrection: Genetic etiology of truncus arteriosus excluding 22q11.2 deletion syndrome and identification of c.1617del, a prevalent variant in TMEM260, in the Japanese population.
Not available
S-EPMC11043029 | biostudies-literature
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