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Search ...
Go!
Schema
>
EntityWithAccessionedSequence
>
Entries
PDGFRA S601P [plasma membrane]
Show undefined attributes
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compartment
[Compartment:876] plasma membrane
created
[InstanceEdit:9673601] Rothfels, Karen, 2020年01月08日
crossReference
[DatabaseIdentifier:11945511] Mondo:0015691
[DatabaseIdentifier:11944892] Mondo:0004992
dbId
9673600
disease
[Disease:1500689] cancer
[Disease:9672476] hypereosinophilic syndrome
displayName
PDGFRA S601P [plasma membrane]
endCoordinate
1089
hasModifiedResidue
[ReplacedResidue:9672474] L-serine 601 replaced with L-proline
inDisease
true
literatureReference
[LiteratureReference:9673492] A novel FIP1L1-PDGFRA mutant destabilizing the inactive conformation of the kinase domain in chronic eosinophilic leukemia/hypereosinophilic syndrome
maxDepth
1
memberOf
[DefinedSet:R-HSA-9673718] sorafenib-resistant PDGFR mutants [plasma membrane] - Homo sapiens
[DefinedSet:R-HSA-9672125] imatinib-resistant PDGFR mutants [plasma membrane] - Homo sapiens
name
PDGFRA S601P
Alpha platelet-derived growth factor receptor
PGDS_HUMAN
referenceEntity
[ReferenceGeneProduct:uniprot:P16234] UniProt:P16234 PDGFRA
referenceType
ReferenceGeneProduct
schemaClass
EntityWithAccessionedSequence
species
[Species:48887] Homo sapiens
stId
R-HSA-9673600
startCoordinate
24
Referrals
(hasMember)
[DefinedSet:R-HSA-9672125] imatinib-resistant PDGFR mutants [plasma membrane]
[DefinedSet:R-HSA-9673718] sorafenib-resistant PDGFR mutants [plasma membrane]
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