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Details on Person Jassal, Bijay, 2014-09-12

Class:IdInstanceEdit:5623034
_displayNameJassal, Bijay, 2014-09-12
_timestamp2014-09-12 15:02:54
author[Person:73447] Jassal, Bijay
dateTime2014-09-12 19:02:15
(authored)[FailedReaction:5623051] Defective RHAG does not transport NH4+ from cytosol to extracellular region (rbc) [Homo sapiens]
(created)[ReplacedResidue:5623019] glycine 280 replaced with L-arginine
[Person:5623020] Raynal, V
[EntityWithAccessionedSequence:5623021] RHAG G280R [plasma membrane] [Homo sapiens]
[LiteratureReference:5623022] The Rh protein family: gene evolution, membrane biology, and disease association
[Person:5623023] Colin, Yves
[EntityWithAccessionedSequence:5623024] RHAG V270I [plasma membrane] [Homo sapiens]
[EntityWithAccessionedSequence:5623025] RHAG A363Lfs*15 [plasma membrane] [Homo sapiens]
[EntityWithAccessionedSequence:5623026] RHAG S79N [plasma membrane] [Homo sapiens]
[ReplacedResidue:5623027] L-serine 79 replaced with L-asparagine
[Person:5623028] Cherif-Zahar, B
List all 36 refering instances
(edited)[FailedReaction:5623051] Defective RHAG does not transport NH4+ from cytosol to extracellular region (rbc) [Homo sapiens]
(modified)[Summation:444403] The human gene RHAG encodes a Rhesus blood group family type...
[Reaction:444416] RHAG transports NH4+ from cytosol to extracellular region (red blood cells) [Homo sapiens]
[Pathway:5619042] Defective RHAG causes regulator type Rh-null hemolytic anemia (RHN) [Homo sapiens]
[Summation:5621882] Cytosolic hexokinase 1 (HK1), together with isoforms HK2 and...
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No pathways have been reviewed or authored by Jassal, Bijay, 2014-09-12 (5623034)