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Schema
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Pathway
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Entries
Defective SLCO1B1 causes hyperbilirubinemia, Rotor type (HBLRR)
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authored
[InstanceEdit:5619074] Jassal, Bijay, 2014年08月22日
created
[InstanceEdit:5619074] Jassal, Bijay, 2014年08月22日
crossReference
[DatabaseIdentifier:11945007] Mondo:0002408
dbId
5619110
deleted
[Deleted:9661804] Deletion of instance: 5661182
disease
[Disease:5605024] bilirubin metabolic disorder
displayName
Defective SLCO1B1 causes hyperbilirubinemia, Rotor type (HBLRR)
edited
[InstanceEdit:5619074] Jassal, Bijay, 2014年08月22日
eventOf
[Pathway:R-HSA-5619102] SLC transporter disorders - Homo sapiens
hasDiagram
true
hasEHLD
false
hasEvent
[FailedReaction:R-HSA-5661184] Defective SLCO1B1 does not transport BIL from extracellular region (blood) to cytosol (hepatocyte) - Homo sapiens
isInDisease
true
isInferred
false
lastUpdatedDate
2019年12月10日
literatureReference
[LiteratureReference:5661196] Complete OATP1B1 and OATP1B3 deficiency causes human Rotor syndrome by interrupting conjugated bilirubin reuptake into the liver
[LiteratureReference:5605017] New insights in bilirubin metabolism and their clinical implications
[LiteratureReference:5661193] The roles of MRP2, MRP3, OATP1B1, and OATP1B3 in conjugated hyperbilirubinemia
maxDepth
2
modified
[InstanceEdit:9847082] Weiser, Joel, 2023年10月12日
name
Defective SLCO1B1 causes hyperbilirubinemia, Rotor type (HBLRR)
normalPathway
[Pathway:R-HSA-189445] Metabolism of porphyrins
releaseDate
2015年09月22日
reviewStatus
[ReviewStatus:9821382] five stars
reviewed
[InstanceEdit:6789776] Broer, Stefan, 2015年08月04日
revised
[InstanceEdit:9661807] Jassal, Bijay, 2019年09月18日
schemaClass
Pathway
species
[Species:48887] Homo sapiens
stId
R-HSA-5619110
summation
[Summation:5661203] The solute carrier organic anion transporter family member 1...
updateTrackers
[UpdateTracker:9777420] Update Tracker - [Pathway:5619110] Defective SLCO1B1 causes hyperbilirubinemia, Rotor type (HBLRR) - v71:[modifyText, updateContainedRLE]
[UpdateTracker:9778188] Update Tracker - [Pathway:5619110] Defective SLCO1B1 causes hyperbilirubinemia, Rotor type (HBLRR) - v68:[updateContainedRLE]
Referrals
(updatedInstance)
[UpdateTracker:9777420] Update Tracker - [Pathway:5619110] Defective SLCO1B1 causes hyperbilirubinemia, Rotor type (HBLRR) - v71:[modifyText, updateContainedRLE]
[UpdateTracker:9778188] Update Tracker - [Pathway:5619110] Defective SLCO1B1 causes hyperbilirubinemia, Rotor type (HBLRR) - v68:[updateContainedRLE]
(replacementInstances)
[Deleted:9661804] Deletion of instance: 5661182
(hasEvent)
[Pathway:R-HSA-5619102] SLC transporter disorders
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