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Details on Person FKTN transfers RboP to GalNAc-GlcNAc-ManP-DAG1

Class:IdReaction:9940735
_displayNameFKTN transfers RboP to GalNAc-GlcNAc-ManP-DAG1
_doReleaseTRUE
_timestamp2025-06-02 08:57:56
authored[InstanceEdit:9940797] Stephan, Ralf, 2025-03-02
catalystActivity[CatalystActivity:9940857] phosphotransferase activity, for other substituted phosphate groups of FKRP:FKTN:RXYLT1 [Golgi membrane]
compartment[Compartment:17963] Golgi lumen
[Compartment:20699] Golgi membrane
created[InstanceEdit:9940703] Stephan, Ralf, 2025-03-06
crossReference[DatabaseIdentifier:9940803] RHEA:36552
edited[InstanceEdit:9947109] Stephan, Ralf, 2025-05-01
input[SimpleEntity:9940856] CDP-ribitol [Golgi lumen]
[EntityWithAccessionedSequence:8932424] Core M1,2,3-DAG1 [Golgi lumen] [Homo sapiens]
internalReviewed[InstanceEdit:9944933] D'Eustachio, Peter, 2025-04-08
[InstanceEdit:9953298] Stephan, Ralf, 2025-06-02
isChimericFALSE
literatureReference[LiteratureReference:9940675] Cell endogenous activities of fukutin and FKRP coexist with the ribitol xylosyltransferase, TMEM5
[LiteratureReference:9940676] Identification of a Post-translational Modification with Ribitol-Phosphate and Its Defect in Muscular Dystrophy
[LiteratureReference:9940685] Novel mutations and genotype-phenotype relationships in 107 families with Fukuyama-type congenital muscular dystrophy (FCMD)
[LiteratureReference:9940791] A homozygous nonsense mutation in the fukutin gene causes a Walker-Warburg syndrome phenotype
[LiteratureReference:9940719] Fukutin gene mutations in steroid-responsive limb girdle muscular dystrophy
[LiteratureReference:9940738] Carbohydrate-binding domain of the POMGnT1 stem region modulates O-mannosylation sites of α-dystroglycan
[LiteratureReference:9940819] Molecular interaction between fukutin and POMGnT1 in the glycosylation pathway of alpha-dystroglycan
[LiteratureReference:5617077] Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1
[LiteratureReference:9940822] POMGnT1 mutations in congenital muscular dystrophy: genotype-phenotype correlation and expanded clinical spectrum
[LiteratureReference:9940807] Mild POMGnT1 mutations underlie a novel limb-girdle muscular dystrophy variant
modified[InstanceEdit:9941578] Stephan, Ralf, 2025-03-09
[InstanceEdit:9942597] Stephan, Ralf, 2025-03-18
[InstanceEdit:9944934] Stephan, Ralf, 2025-04-08
[InstanceEdit:9947108] Stephan, Ralf, 2025-05-01
[InstanceEdit:9947328] Stephan, Ralf, 2025-05-05
[InstanceEdit:9948073] Stephan, Ralf, 2025-05-15
[InstanceEdit:9953299] Stephan, Ralf, 2025-06-02
[InstanceEdit:9953301] Stephan, Ralf, 2025-06-02
nameFKTN transfers RboP to GalNAc-GlcNAc-ManP-DAG1
output[SimpleEntity:727810] CMP [Golgi lumen]
[SimpleEntity:425969] H+ [Golgi lumen]
[EntityWithAccessionedSequence:9940763] RboP-GalNAc-GlcNAc-Man6P-DAG1 [Golgi lumen] [Homo sapiens]
precedingEvent
previousReviewStatus[ReviewStatus:9821384] two stars
releaseDate2025-06-18
reviewed[InstanceEdit:9947107] Zaru, Rossana, 2025-05-01
[InstanceEdit:9948068] Hill, David P, 2025-05-15
[InstanceEdit:9953300] Matthews, Lisa, 2025-06-02
reviewStatus[ReviewStatus:9821382] five stars
species[Species:48887] Homo sapiens
stableIdentifier[StableIdentifier:9940890] R-HSA-9940735.1
structureModified[InstanceEdit:9941578] Stephan, Ralf, 2025-03-09
[InstanceEdit:9948073] Stephan, Ralf, 2025-05-15
summation[Summation:9940688] The ribitol-5-phosphate transferase FKTN subunit of the FKRP...
(hasEvent)[Pathway:9939291] Matriglycan biosynthesis on DAG1 [Homo sapiens]
(precedingEvent)[Reaction:9940756] FKRP dimer transfers RboP to matriglycan chain [Homo sapiens]
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No pathways have been reviewed or authored by FKTN transfers RboP to GalNAc-GlcNAc-ManP-DAG1 (9940735)