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Details on Person Jassal, Bijay, 2014-12-11

Class:IdInstanceEdit:5656252
_displayNameJassal, Bijay, 2014-12-11
_timestamp2014-12-11 17:33:13
author[Person:73447] Jassal, Bijay
dateTime2014-12-11 22:31:02
(authored)[FailedReaction:5656219] Defective SLC4A4 does not cotransport Na+ with 3HCO3- [Homo sapiens]
[FailedReaction:5656248] Defective SLC4A1 does not exchange Cl- for HCO3- (in erythrocytes) [Homo sapiens]
(created)[LiteratureReference:5656201] Molecular mechanisms of renal and extrarenal manifestations caused by inactivation of the electrogenic Na(+)-HCO3 (-) cotransporter NBCe1
[LiteratureReference:5656202] A novel missense mutation in the sodium bicarbonate cotransporter (NBCe1/SLC4A4) causes proximal tubular acidosis and glaucoma through ion transport defects
[ReplacedResidue:5656203] L-alanine 799 replaced with L-valine
[Person:5656204] Cha, S H
[Person:5656205] Shimadzu, Mitsunobu
[EntityWithAccessionedSequence:5656206] SLC4A4 A799V [plasma membrane] [Homo sapiens]
[Person:5656207] Angle, Nathan
[EntityWithAccessionedSequence:5656208] SLC4A4 R298S [plasma membrane] [Homo sapiens]
[DefinedSet:5656209] SLC4A4 mutants [plasma membrane] [Homo sapiens]
[EntityWithAccessionedSequence:5656210] SLC4A4 R510H [plasma membrane] [Homo sapiens]
List all 74 refering instances
(edited)[FailedReaction:5656219] Defective SLC4A4 does not cotransport Na+ with 3HCO3- [Homo sapiens]
[FailedReaction:5656248] Defective SLC4A1 does not exchange Cl- for HCO3- (in erythrocytes) [Homo sapiens]
(modified)[Reaction:425483] SLC4A5,7,9 cotransport Na+ with 3HCO3- [Homo sapiens]
[Summation:425490] The proteins responsible for the exchange of Cl- with HCO3- ...
[DefinedSet:425547] SLC4A5,7,9 [plasma membrane] [Homo sapiens]
[Summation:425568] Members of the SLC4A family couple the transport of bicarbon...
[CatalystActivity:425592] sodium:bicarbonate symporter activity of SLC4A5,7,9 [plasma membrane]
[Pathway:5619050] Defective SLC4A1 causes hereditary spherocytosis type 4 (HSP4), distal renal tubular acidosis (dRTA) and dRTA with hemolytic anemia (dRTA-HA) [Homo sapiens]
[Pathway:5619054] Defective SLC4A4 causes renal tubular acidosis, proximal, with ocular abnormalities and mental retardation (pRTA-OA) [Homo sapiens]
[Pathway:5619102] SLC transporter disorders [Homo sapiens]
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No pathways have been reviewed or authored by Jassal, Bijay, 2014-12-11 (5656252)