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Search ...
Go!
Schema
>
EntityWithAccessionedSequence
>
Entries
p16INK4A A60V [cytosol]
Show undefined attributes
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compartment
[Compartment:70101] cytosol
created
[InstanceEdit:9632213] Orlic-Milacic, Marija, 2018年12月14日
crossReference
[DatabaseIdentifier:11945473] Mondo:0002297
[DatabaseIdentifier:11945472] Mondo:0000536
[DatabaseIdentifier:11944976] Mondo:0005061
[DatabaseIdentifier:11944898] Mondo:0005105
[DatabaseIdentifier:11944892] Mondo:0004992
[DatabaseIdentifier:9632210] COSMIC:COSV58685686
dbId
9632212
disease
[Disease:1500689] cancer
[Disease:8853117] lung adenocarcinoma
[Disease:9630850] pharynx squamous cell carcinoma
[Disease:9632211] epidermal appendage tumor
[Disease:1614289] melanoma
displayName
p16INK4A A60V [cytosol]
endCoordinate
156
hasModifiedResidue
[ReplacedResidue:9632200] L-alanine 60 replaced with L-valine
inDisease
true
literatureReference
[LiteratureReference:9631273] Functional, structural, and genetic evaluation of 20 CDKN2A germ line mutations identified in melanoma-prone families or patients
maxDepth
1
memberOf
[CandidateSet:R-HSA-9630826] p16INK4A LoF mutants (CDK4) [cytosol] - Homo sapiens
modified
[InstanceEdit:9645190] Orlic-Milacic, Marija, 2019年05月06日
name
p16INK4A A60V
p16INK4A Ala60Val
CDKN2A A60V
CDKN2A Ala60Val
referenceEntity
[ReferenceGeneProduct:uniprot:P42771] UniProt:P42771 CDKN2A
referenceType
ReferenceGeneProduct
schemaClass
EntityWithAccessionedSequence
species
[Species:48887] Homo sapiens
stId
R-HSA-9632212
startCoordinate
1
Referrals
(hasMember)
[CandidateSet:R-HSA-9630826] p16INK4A LoF mutants (CDK4) [cytosol]
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