Reactome | SLC34A1 A48F [plasma membrane]

Schema > EntityWithAccessionedSequence > Entries

compartment	[Compartment:876] plasma membrane
created	[InstanceEdit:5651695] Jassal, Bijay, 2014-11-24
crossReference	[DatabaseIdentifier:12020998] Mondo:0000313
dbId	5651701
disease	[Disease:5651689] hypophosphatemia [Disease:5651669] nephrolithiasis [Disease:5638228] renal tubular transport disease
displayName	SLC34A1 A48F [plasma membrane]
endCoordinate	639
hasModifiedResidue	[ReplacedResidue:5651698] L-alanine 48 replaced with L-phenylalanine
inDisease	true
maxDepth	1
memberOf	[DefinedSet:R-HSA-5651692] SLC34A1 mutants [plasma membrane] - Homo sapiens
name	SLC34A1 A48F Sodium-dependent phosphate transport protein 2A NPT2A_HUMAN
referenceEntity	[ReferenceGeneProduct:uniprot:Q06495] UniProt:Q06495 SLC34A1
referenceType	ReferenceGeneProduct
schemaClass	EntityWithAccessionedSequence
species	[Species:48887] Homo sapiens
stId	R-HSA-5651701
startCoordinate	1

(hasMember)

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