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Go!
Schema
>
EntityWithAccessionedSequence
>
Entries
SLC6A19 R240* [plasma membrane]
Show undefined attributes
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compartment
[Compartment:876] plasma membrane
created
[InstanceEdit:5659745] Jassal, Bijay, 2014年12月23日
crossReference
[DatabaseIdentifier:11945117] Mondo:0009324
dbId
5659732
disease
[Disease:5659739] Hartnup disease
displayName
SLC6A19 R240* [plasma membrane]
endCoordinate
634
hasModifiedResidue
[NonsenseMutation:5659744] Nonsense mutation at L-arginine 240
inDisease
true
maxDepth
1
memberOf
[DefinedSet:R-HSA-5659731] SLC6A19 mutants [plasma membrane] - Homo sapiens
name
SLC6A19 R240*
Sodium-dependent neutral amino acid transporter B(0)
referenceEntity
[ReferenceGeneProduct:uniprot:Q695T7] UniProt:Q695T7 SLC6A19
referenceType
ReferenceGeneProduct
schemaClass
EntityWithAccessionedSequence
species
[Species:48887] Homo sapiens
stId
R-HSA-5659732
startCoordinate
1
Referrals
(hasMember)
[DefinedSet:R-HSA-5659731] SLC6A19 mutants [plasma membrane]
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