Reactome | CYP11B2 R181W [mitochondrial inner membrane]

Schema > EntityWithAccessionedSequence > Entries

compartment	[Compartment:70616] mitochondrial inner membrane
created	[InstanceEdit:5600619] Jassal, Bijay, 2014-06-12
crossReference	[DatabaseIdentifier:12020861] Mondo:0005523
dbId	5600621
disease	[Disease:3769465] steroid inherited metabolic disorder
displayName	CYP11B2 R181W [mitochondrial inner membrane]
endCoordinate	503
hasModifiedResidue	[ReplacedResidue:5600632] L-arginine 181 replaced with L-tryptophan
inDisease	true
maxDepth	1
memberOf	[DefinedSet:R-HSA-5600661] CYP11B2 mutants [mitochondrial inner membrane] - Homo sapiens
modified	[InstanceEdit:5600670] Jassal, Bijay, 2014-06-12
name	CYP11B2 R181W Cytochrome P450 11B2 CPN2_HUMAN
referenceEntity	[ReferenceGeneProduct:uniprot:P19099] UniProt:P19099 CYP11B2
referenceType	ReferenceGeneProduct
schemaClass	EntityWithAccessionedSequence
species	[Species:48887] Homo sapiens
stId	R-HSA-5600621
startCoordinate	25

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