Reactome | SLC2A10 mutants [plasma membrane]

Schema > DefinedSet > Entries

catalystActivities	[CatalystActivity:9631817] D-glucose transmembrane transporter activity of SLC2A10 mutants [plasma membrane]
compartment	[Compartment:876] plasma membrane
created	[InstanceEdit:5632829] Jassal, Bijay, 2014-10-29
crossReference	[DatabaseIdentifier:12020991] Mondo:0008818
dbId	5632783
disease	[Disease:5632822] arterial tortuosity syndrome
displayName	SLC2A10 mutants [plasma membrane]
hasMember	[EntityWithAccessionedSequence:R-HSA-5632806] SLC2A10 G426W [plasma membrane] - Homo sapiens [EntityWithAccessionedSequence:R-HSA-5632857] SLC2A10 G445Efs40 [plasma membrane] - Homo sapiens [EntityWithAccessionedSequence:R-HSA-5632837] SLC2A10 R132W [plasma membrane] - Homo sapiens [EntityWithAccessionedSequence:R-HSA-5632855] SLC2A10 S81R [plasma membrane] - Homo sapiens [EntityWithAccessionedSequence:R-HSA-5632845] SLC2A10 V321Cfs71 [plasma membrane] - Homo sapiens [EntityWithAccessionedSequence:R-HSA-5632790] SLC2A10 W170* [plasma membrane] - Homo sapiens
inDisease	true
maxDepth	2
modified	[InstanceEdit:5638236] Jassal, Bijay, 2014-11-13
name	SLC2A10 mutants
schemaClass	DefinedSet
species	[Species:48887] Homo sapiens
stId	R-HSA-5632783

(diseaseEntity)	[EntityFunctionalStatus:5632797] loss_of_function of SLC2A10 mutants [plasma membrane]
(physicalEntity)	[CatalystActivity:9631817] D-glucose transmembrane transporter activity of SLC2A10 mutants [plasma membrane]