Reactome | RHAG mutants [plasma membrane]

Schema > DefinedSet > Entries

catalystActivities	[CatalystActivity:9631834] ammonium channel activity of RHAG mutants [plasma membrane]
compartment	[Compartment:876] plasma membrane
created	[InstanceEdit:5623034] Jassal, Bijay, 2014-09-12
crossReference	[DatabaseIdentifier:12021000] Mondo:0019107
dbId	5623052
disease	[Disease:5623555] Rh deficiency syndrome
displayName	RHAG mutants [plasma membrane]
hasMember	[EntityWithAccessionedSequence:R-HSA-5623025] RHAG A363Lfs15 [plasma membrane] - Homo sapiens [EntityWithAccessionedSequence:R-HSA-5623021] RHAG G280R [plasma membrane] - Homo sapiens [EntityWithAccessionedSequence:R-HSA-5623035] RHAG G380V [plasma membrane] - Homo sapiens [EntityWithAccessionedSequence:R-HSA-5623046] RHAG P52Dfs57 [plasma membrane] - Homo sapiens [EntityWithAccessionedSequence:R-HSA-5623026] RHAG S79N [plasma membrane] - Homo sapiens [EntityWithAccessionedSequence:R-HSA-5623024] RHAG V270I [plasma membrane] - Homo sapiens
inDisease	true
maxDepth	2
modified	[InstanceEdit:5623756] Jassal, Bijay, 2014-09-19
name	RHAG mutants
schemaClass	DefinedSet
species	[Species:48887] Homo sapiens
stId	R-HSA-5623052

(diseaseEntity)	[EntityFunctionalStatus:5623050] loss_of_function of RHAG mutants [plasma membrane]
(physicalEntity)	[CatalystActivity:9631834] ammonium channel activity of RHAG mutants [plasma membrane]