Suneet Shukla

 ORCID
Reviewed Pathways (11/11)
Date Identifier Pathway Reference
2015-09-15 R-HSA-5683329 Defective ABCD4 causes methylmalonic aciduria and homocystinuria, cblj type (MAHCJ) BibTex
2015-04-28 R-HSA-5619084 ABC transporter disorders BibTex
2015-09-15 R-HSA-5682294 Defective ABCA12 causes autosomal recessive congenital ichthyosis type 4B BibTex
2015-09-15 R-HSA-5679090 Defective ABCG8 causes gallbladder disease 4 and sitosterolemia BibTex
2015-09-15 R-HSA-5683678 Defective ABCA3 causes pulmonary surfactant metabolism dysfunction type 3 (SMDP3) BibTex
2015-09-15 R-HSA-5679096 Defective ABCG5 causes sitosterolemia BibTex
2015-09-15 R-HSA-5679001 Defective ABCC2 causes Dubin-Johnson syndrome BibTex
2015-09-15 R-HSA-5690338 Defective ABCC6 causes pseudoxanthoma elasticum (PXE) BibTex
2015-09-15 R-HSA-5682113 Defective ABCA1 causes Tangier disease BibTex
2015-09-15 R-HSA-5684045 Defective ABCD1 causes adrenoleukodystrophy (ALD) BibTex
2015-09-15 R-HSA-5683177 Defective ABCC8 can cause hypoglycemias and hyperglycemias BibTex
Reviewed Reactions (11/11)
Date Identifier Reaction Reference
2015-09-15 R-HSA-5683325 Defective ABCD4 does not transport Cbl from lysosomal lumen to cytosol BibTex
2015-09-15 R-HSA-5682311 Defective ABCA12 does not transport lipids from cytosol to extracellular region BibTex
2015-09-15 R-HSA-5679101 Defective ABCG8 (in ABCG5:ABCG8) does not transport sterols from cytosol to extracellular region BibTex
2015-09-15 R-HSA-5683672 Defective ABCA3 does not transport PC, PG from ER membrane to lamellar body BibTex
2015-09-15 R-HSA-5679145 Defective ABCG5 (in ABCG5:ABCG8) does not transport sterols from cytosol to extracellular region BibTex
2015-09-15 R-HSA-5679031 Defective ABCC2 does not transport BMG,BDG from cytosol to extracellular region BibTex
2015-09-15 R-HSA-5690340 Defective ABCC6 does not transport organic anion from cytosol to extracellular region BibTex
2015-09-15 R-HSA-5682111 Defective ABCA1 does not transport CHOL from transport vesicle membrane to plasma membrane BibTex
2015-09-15 R-HSA-5684043 Defective ABCD1 does not transfer LCFAs from cytosol to peroxisomal matrix BibTex
2015-09-15 R-HSA-5683113 Defective ABCC8 does not form functional KATP channels, causing hyperinsulinemic hypoglycemia BibTex
2015-09-15 R-HSA-5683209 Activating ABCC8 mutants cause hyperglycemia in permanent neonatal diabetes mellitus (PNDM) and transient neonatal DM (TNDM). BibTex