Reactome | SLC27A4 R583H [plasma membrane]

Schema > EntityWithAccessionedSequence > Entries

compartment	[Compartment:876] plasma membrane
created	[InstanceEdit:5627904] Jassal, Bijay, 2014-10-23
crossReference	[DatabaseIdentifier:12021020] Mondo:0006025
dbId	5627897
disease	[Disease:5627902] autosomal recessive disease
displayName	SLC27A4 R583H [plasma membrane]
endCoordinate	643
hasModifiedResidue	[ReplacedResidue:5627898] L-arginine 583 replaced with L-histidine
inDisease	true
maxDepth	1
memberOf	[DefinedSet:R-HSA-5627903] SLC27A4 mutants [plasma membrane] - Homo sapiens
name	SLC27A4 R583H FATP4 Long-chain fatty acid transport protein 4 S27A4_HUMAN
referenceEntity	[ReferenceGeneProduct:uniprot:Q6P1M0] UniProt:Q6P1M0 SLC27A4
referenceType	ReferenceGeneProduct
schemaClass	EntityWithAccessionedSequence
species	[Species:48887] Homo sapiens
stId	R-HSA-5627897
startCoordinate	1

(hasMember)

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