Reactome | SLC4A1 mutants [plasma membrane]

Schema > DefinedSet > Entries

catalystActivities	[CatalystActivity:9631873] solute:inorganic anion antiporter activity of SLC4A1 mutants [plasma membrane]
compartment	[Compartment:876] plasma membrane
created	[InstanceEdit:5657850] Jassal, Bijay, 2014-12-16
crossReference	[DatabaseIdentifier:12021006] Mondo:0019350
dbId	5657826
disease	[Disease:5656223] hereditary spherocytosis [Disease:5656215] renal tubular acidosis [Disease:5602914] hemolytic anemia
displayName	SLC4A1 mutants [plasma membrane]
hasMember	[EntityWithAccessionedSequence:R-HSA-5657836] SLC4A1 G701D [plasma membrane] - Homo sapiens [EntityWithAccessionedSequence:R-HSA-5657843] SLC4A1 R589C [plasma membrane] - Homo sapiens [EntityWithAccessionedSequence:R-HSA-5657833] SLC4A1 R589H [plasma membrane] - Homo sapiens [EntityWithAccessionedSequence:R-HSA-5657854] SLC4A1 S613F [plasma membrane] - Homo sapiens [EntityWithAccessionedSequence:R-HSA-5657845] SLC4A1 V488M [plasma membrane] - Homo sapiens [EntityWithAccessionedSequence:R-HSA-5657828] SLC4A1 V850del [plasma membrane] - Homo sapiens [EntityWithAccessionedSequence:R-HSA-5657855] SLC4A1 E90K [plasma membrane] - Homo sapiens
inDisease	true
maxDepth	2
name	SLC4A1 mutants
schemaClass	DefinedSet
species	[Species:48887] Homo sapiens
stId	R-HSA-5657826

(diseaseEntity)	[EntityFunctionalStatus:5657848] loss_of_function of SLC4A1 mutants [plasma membrane]
(physicalEntity)	[CatalystActivity:9631873] solute:inorganic anion antiporter activity of SLC4A1 mutants [plasma membrane]