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Schema
>
DefinedSet
>
Entries
ABCC9 mutants [plasma membrane]
Show undefined attributes
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compartment
[Compartment:876] plasma membrane
componentOf
[Complex:R-HSA-9631856] ABCC9 mutants:KCNJ11 [plasma membrane] - Homo sapiens
created
[InstanceEdit:5678429] Jassal, Bijay, 2015-02-24
dbId
5678456
disease
[Disease:5678419] dilated cardiomyopathy
[Disease:5678510] familial atrial fibrillation
[Disease:5678508] hypertrichosis
[Disease:3656241] osteochondrodysplasia
displayName
ABCC9 mutants [plasma membrane]
hasMember
[EntityWithAccessionedSequence:R-HSA-5678421] ABCC9 L1524Kfs*5 [plasma membrane] - Homo sapiens
[EntityWithAccessionedSequence:R-HSA-5678458] ABCC9 T1547I [plasma membrane] - Homo sapiens
[EntityWithAccessionedSequence:R-HSA-5678947] ABCC9 A1513T [plasma membrane] - Homo sapiens
[EntityWithAccessionedSequence:R-HSA-5678850] ABCC9 C1043Y [plasma membrane] - Homo sapiens
[EntityWithAccessionedSequence:R-HSA-5678818] ABCC9 H60Y [plasma membrane] - Homo sapiens
[EntityWithAccessionedSequence:R-HSA-5678820] ABCC9 R1116H [plasma membrane] - Homo sapiens
[EntityWithAccessionedSequence:R-HSA-5678930] ABCC9 R1154Q [plasma membrane] - Homo sapiens
[EntityWithAccessionedSequence:R-HSA-5678781] ABCC9 R1154W [plasma membrane] - Homo sapiens
[EntityWithAccessionedSequence:R-HSA-5678912] ABCC9 S1020P [plasma membrane] - Homo sapiens
inDisease
true
modified
[InstanceEdit:5678752] Jassal, Bijay, 2015-02-26
name
ABCC9 mutants
schemaClass
DefinedSet
species
[Species:48887] Homo sapiens
stId
R-HSA-5678456
Referrals
(hasComponent)
[Complex:R-HSA-9631856] ABCC9 mutants:KCNJ11 [plasma membrane]
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