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Go!
Schema
>
EntityWithAccessionedSequence
>
Entries
p-S621-RAF1 P261T [cytosol]
Show undefined attributes
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compartment
[Compartment:70101] cytosol
created
[InstanceEdit:9656116] Rothfels, Karen, 2019年07月27日
crossReference
[DatabaseIdentifier:11944924] Mondo:0018997
[DatabaseIdentifier:11944898] Mondo:0005105
[DatabaseIdentifier:9655967] COSMIC:COSV52576947
dbId
9656115
disease
[Disease:1614289] melanoma
[Disease:6802289] Noonan syndrome
displayName
p-S621-RAF1 P261T [cytosol]
endCoordinate
648
hasModifiedResidue
[ModifiedResidue:109785] O-phospho-L-serine at 621
[ReplacedResidue:9655914] L-proline 261 replaced with L-threonine
inDisease
true
literatureReference
[LiteratureReference:9655515] Molecular and clinical analysis of RAF1 in Noonan syndrome and related disorders: dephosphorylation of serine 259 as the essential mechanism for mutant activation
[LiteratureReference:9655523] Spectrum of mutations in Noonan syndrome and their correlation with phenotypes
maxDepth
1
memberOf
[CandidateSet:R-HSA-9656159] p-S621 RAF1 CR2 mutants [cytosol] - Homo sapiens
name
p-S621-RAF1 P261T
RAF proto-oncogene serine/threonine-protein kinase
Raf-1
C-RAF
cRaf
referenceEntity
[ReferenceGeneProduct:uniprot:P04049] UniProt:P04049 RAF1
referenceType
ReferenceGeneProduct
schemaClass
EntityWithAccessionedSequence
species
[Species:48887] Homo sapiens
stId
R-HSA-9656115
startCoordinate
1
Referrals
(hasMember)
[CandidateSet:R-HSA-9656159] p-S621 RAF1 CR2 mutants [cytosol]
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