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Search ...
Go!
Schema
>
EntityWithAccessionedSequence
>
Entries
SRD5A3 R142* [endoplasmic reticulum membrane]
Show undefined attributes
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compartment
[Compartment:12045] endoplasmic reticulum membrane
created
[InstanceEdit:4755549] Jassal, B, 2013年10月25日
crossReference
[DatabaseIdentifier:11945016] Mondo:0005500
dbId
4755594
disease
[Disease:3781892] congenital disorder of glycosylation type I
displayName
SRD5A3 R142* [endoplasmic reticulum membrane]
endCoordinate
318
hasModifiedResidue
[NonsenseMutation:4755567] Nonsense mutation at L-arginine 142
inDisease
true
maxDepth
1
memberOf
[DefinedSet:R-HSA-4755569] SRD5A3 mutants [endoplasmic reticulum membrane] - Homo sapiens
modified
[InstanceEdit:5649739] Jassal, Bijay, 2014年11月21日
name
SRD5A3 R142*
3-oxo-5-alpha-steroid 4-dehydrogenase 3
S5A3_HUMAN
referenceEntity
[ReferenceGeneProduct:uniprot:Q9H8P0] UniProt:Q9H8P0 SRD5A3
referenceType
ReferenceGeneProduct
schemaClass
EntityWithAccessionedSequence
species
[Species:48887] Homo sapiens
stId
R-HSA-4755594
startCoordinate
1
Referrals
(hasMember)
[DefinedSet:R-HSA-4755569] SRD5A3 mutants [endoplasmic reticulum membrane]
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