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Go!
Schema
>
DefinedSet
>
Entries
SLC11A2 mutants [plasma membrane]
Show undefined attributes
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catalystActivities
[CatalystActivity:9631722] iron ion transmembrane transporter activity of SLC11A2 mutants [plasma membrane]
compartment
[Compartment:876] plasma membrane
created
[InstanceEdit:5623756] Jassal, Bijay, 2014年09月19日
crossReference
[DatabaseIdentifier:11945141] Mondo:0000387
dbId
5623738
disease
[Disease:5623576] hypochromic microcytic anemia
displayName
SLC11A2 mutants [plasma membrane]
hasMember
[EntityWithAccessionedSequence:R-HSA-5623707] SLC11A2 L104_P142del [plasma membrane] - Homo sapiens
[EntityWithAccessionedSequence:R-HSA-5623732] SLC11A2 E399D [plasma membrane] - Homo sapiens
[EntityWithAccessionedSequence:R-HSA-5623771] SLC11A2 G212V [plasma membrane] - Homo sapiens
[EntityWithAccessionedSequence:R-HSA-5623758] SLC11A2 R416C [plasma membrane] - Homo sapiens
[EntityWithAccessionedSequence:R-HSA-5623747] SLC11A2 V114del [plasma membrane] - Homo sapiens
inDisease
true
maxDepth
2
name
SLC11A2 mutants
schemaClass
DefinedSet
species
[Species:48887] Homo sapiens
stId
R-HSA-5623738
Referrals
(diseaseEntity)
[EntityFunctionalStatus:5623709] loss_of_function of SLC11A2 mutants [plasma membrane]
(physicalEntity)
[CatalystActivity:9631722] iron ion transmembrane transporter activity of SLC11A2 mutants [plasma membrane]
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