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Search ...
Go!
Schema
>
EntityWithAccessionedSequence
>
Entries
ALG14 P65L [endoplasmic reticulum membrane]
Show undefined attributes
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compartment
[Compartment:12045] endoplasmic reticulum membrane
created
[InstanceEdit:5633234] Jassal, Bijay, 2014年10月31日
crossReference
[DatabaseIdentifier:11945045] Mondo:0018940
dbId
5633218
disease
[Disease:5633237] congenital myasthenic syndrome
displayName
ALG14 P65L [endoplasmic reticulum membrane]
endCoordinate
216
hasModifiedResidue
[ReplacedResidue:5633242] L-proline 65 replaced with L-leucine
inDisease
true
maxDepth
1
memberOf
[DefinedSet:R-HSA-5633238] ALG14 mutants [endoplasmic reticulum membrane] - Homo sapiens
name
ALG14 P65L
UDP-N-acetylglucosamine transferase subunit ALG14 homolog
ALG14_HUMAN
referenceEntity
[ReferenceGeneProduct:uniprot:Q96F25] UniProt:Q96F25 ALG14
referenceType
ReferenceGeneProduct
schemaClass
EntityWithAccessionedSequence
species
[Species:48887] Homo sapiens
stId
R-HSA-5633218
startCoordinate
1
Referrals
(hasMember)
[DefinedSet:R-HSA-5633238] ALG14 mutants [endoplasmic reticulum membrane]
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