Reactome | F8 Y1699F [Golgi lumen]

Schema > EntityWithAccessionedSequence > Entries

compartment	[Compartment:17963] Golgi lumen
consumedByEvent	[FailedReaction:R-HSA-9668148] F8 variant is not sulfonated at Y1699 - Homo sapiens
created	[InstanceEdit:9668147] Shamovsky, Veronica, 2019-11-19
crossReference	[DatabaseIdentifier:9672536] ClinGen:CA255022
dbId	9668150
displayName	F8 Y1699F [Golgi lumen]
endCoordinate	2351
hasModifiedResidue	[ReplacedResidue:9665825] L-tyrosine 1699 replaced with L-phenylalanine
inDisease	false
maxDepth	1
modified	[InstanceEdit:9672533] Shamovsky, Veronica, 2019-12-27
name	F8 Y1699F Factor VIII precursor Y1699F
referenceEntity	[ReferenceGeneProduct:uniprot:P00451] UniProt:P00451 F8
referenceType	ReferenceGeneProduct
schemaClass	EntityWithAccessionedSequence
species	[Species:48887] Homo sapiens
stId	R-HSA-9668150
startCoordinate	20

(input)	[FailedReaction:R-HSA-9668148] F8 variant is not sulfonated at Y1699
(diseaseEntity)	[EntityFunctionalStatus:9668272] loss_of_function of F8 Y1699F [Golgi lumen]

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