Reactome: A Curated Pathway Database

Query author contributions in Reactome

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Pathways authored by Jassal, Bijay (73447)

DB_ID Name
5252538 Drosophila signaling pathways
15869 Metabolism of nucleotides
2142845 Hyaluronan metabolism
2142850 Hyaluronan biosynthesis and export
2160916 Hyaluronan uptake and degradation
71384 Ethanol oxidation
73614 Pyrimidine salvage
73621 Pyrimidine catabolism
73817 Purine ribonucleoside monophosphate biosynthesis
74217 Purine salvage
74259 Purine catabolism
2179392 EGFR Transactivation by Gastrin
2187335 The retinoid cycle in cones (daylight vision)
2187338 Visual phototransduction
2206305 MPS IIID - Sanfilippo syndrome D
2206307 MPS IIIA - Sanfilippo syndrome A
2206308 MPS IV - Morquio syndrome B
2206281 Mucopolysaccharidoses
2206280 MPS IX - Natowicz syndrome
2206282 MPS IIIB - Sanfilippo syndrome B
2206285 MPS VI - Maroteaux-Lamy syndrome
2206291 MPS IIIC - Sanfilippo syndrome C
2206290 MPS IV - Morquio syndrome A
2206292 MPS VII - Sly syndrome
2206296 MPS II - Hunter syndrome
2206302 MPS I - Hurler syndrome
110478 Insulin signaling pathway
110523 TOR signaling pathway
110524 DINR-mediated activation
110526 Insulin receptor mediated signaling
111885 Opioid Signalling
111931 PKA-mediated phosphorylation of CREB
111933 Calmodulin induced events
111932 CaMK IV-mediated phosphorylation of CREB
111957 Cam-PDE 1 activation
111995 phospho-PLA2 pathway
111997 CaM pathway
111996 Ca-dependent events
112040 G-protein mediated events
112043 PLC beta mediated events
5362517 Signaling by Retinoic Acid
5365859 RA biosynthesis pathway
140179 Amine Oxidase reactions
140180 COX reactions
141334 PAOs oxidise polyamines to amines
141333 Biogenic amines are oxidatively deaminated to aldehydes by MAOA and MAOB
4341670 Defective NEU1 causes sialidosis
3295583 TRP channels
3296482 Defects in vitamin and cofactor metabolism
3296469 Defects in cobalamin (B12) metabolism
156582 Acetylation
156580 Phase II - Conjugation of compounds
156581 Methylation
156587 Amino Acid conjugation
156584 Cytosolic sulfonation of small molecules
156590 Glutathione conjugation
156588 Glucuronidation
156988 Receptor-ligand binding initiates the second proteolytic cleavage of Notch receptor
157052 NICD traffics to nucleus
157118 Signaling by NOTCH
157212 A third proteolytic cleavage releases NICD
159418 Recycling of bile acids and salts
159424 Conjugation of carboxylic acids
163200 Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins.
163210 Formation of ATP by chemiosmotic coupling
163615 PKA activation
166187 Mitochondrial Uncoupling Proteins
170660 Adenylate cyclase activating pathway
170670 Adenylate cyclase inhibitory pathway
170834 Signaling by TGF-beta Receptor Complex
173599 Formation of the active cofactor, UDP-glucuronate
174362 Transport and synthesis of PAPS
174403 Glutathione synthesis and recycling
177128 Conjugation of salicylate with glycine
177135 Conjugation of benzoate with glycine
177162 Conjugation of phenylacetate with glutamine
3323169 Defects in biotin (Btn) metabolism
177929 Signaling by EGFR
180024 DARPP-32 events
5423646 Aflatoxin activation and detoxification
186763 Downstream signal transduction
186797 Signaling by PDGF
189451 Heme biosynthesis
191273 Cholesterol biosynthesis
192105 Synthesis of bile acids and bile salts
193048 Androgen biosynthesis
193144 Estrogen biosynthesis
193368 Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol
193993 Mineralocorticoid biosynthesis
194002 Glucocorticoid biosynthesis
194068 Bile acid and bile salt metabolism
196071 Metabolism of steroid hormones
196108 Pregnenolone biosynthesis
196741 Cobalamin (Cbl, vitamin B12) transport and metabolism
196783 Coenzyme A biosynthesis
196780 Biotin transport and metabolism
196791 Vitamin D (calciferol) metabolism
196807 Nicotinate metabolism
196819 Vitamin B1 (thiamin) metabolism
196836 Vitamin C (ascorbate) metabolism
196849 Metabolism of water-soluble vitamins and cofactors
196854 Metabolism of vitamins and cofactors
197264 Nicotinamide salvaging
202040 G-protein activation
209776 Amine-derived hormones
209822 Glycoprotein hormones
209905 Catecholamine biosynthesis
209931 Serotonin and melatonin biosynthesis
209943 Steroid hormones
209952 Peptide hormone biosynthesis
209968 Thyroxine biosynthesis
211859 Biological oxidations
211897 Cytochrome P450 - arranged by substrate type
211916 Vitamins
211935 Fatty acids
211945 Phase I - Functionalization of compounds
211958 Miscellaneous substrates
211957 Aromatic amines can be N-hydroxylated or N-dealkylated by CYP1A2
211979 Eicosanoids
211976 Endogenous sterols
211981 Xenobiotics
211994 Sterols are 12-hydroxylated by CYP8B1
211999 CYP2E1 reactions
212718 EGFR interacts with phospholipase C-gamma
3359475 Defective MMAA causes methylmalonic aciduria type cblA
3359474 Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC
3359473 Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD
3359478 Defective MUT causes methylmalonic aciduria mut type
3359485 Defective CD320 causes methylmalonic aciduria
3359458 Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF
3359457 Defective GIF causes intrinsic factor deficiency
3359463 Defective CUBN causes hereditary megaloblastic anemia 1
3359462 Defective AMN causes hereditary megaloblastic anemia 1
3359467 Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE
3359471 Defective MMAB causes methylmalonic aciduria type cblB
3359469 Defective MTR causes methylmalonic aciduria and homocystinuria type cblG
3359454 Defective TCN2 causes hereditary megaloblastic anemia
217271 FMO oxidises nucleophiles
3371599 Defective HLCS causes multiple carboxylase deficiency
3371598 Defective BTD causes biotidinase deficiency
4420332 Defective B3GALT6 causes EDSP2 and SEMDJL1
1369007 Mitochondrial ABC transporters
1369062 ABC transporters in lipid homeostasis
5576886 Phase 4 - resting membrane potential
5576893 Phase 2 - plateau phase
5576892 Phase 0 - rapid depolarisation
5576894 Phase 1 - inactivation of fast Na+ channels
5576891 Cardiac conduction
5576890 Phase 3 - rapid repolarisation
5578775 Ion homeostasis
5578768 Physiological factors
5578997 Defective AHCY causes Hypermethioninemia with S-adenosylhomocysteine hydrolase deficiency (HMAHCHD)
5578996 Defective CYP27A1 causes Cerebrotendinous xanthomatosis (CTX)
5578999 Defective GCLC causes Hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency (HAGGSD)
5578998 Defective OPLAH causes 5-oxoprolinase deficiency (OPLAHD)
5578995 Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency)
5579005 Defective CYP4F22 causes Ichthyosis, congenital, autosomal recessive 5 (ARCI5)
5579004 Defective CYP26C1 causes Focal facial dermal dysplasia 4 (FFDD4)
5579007 Defective ACY1 causes encephalopathy
5579006 Defective GSS causes Glutathione synthetase deficiency (GSS deficiency)
5579000 Defective CYP1B1 causes Glaucoma
5579002 Defective UGT1A1 causes hyperbilirubinemia
5579029 Metabolic disorders of biological oxidation enzymes
5579028 Defective CYP17A1 causes Adrenal hyperplasia 5 (AH5)
5579031 Defective ACTH causes Obesity and Pro-opiomelanocortinin deficiency (POMCD)
5579030 Defective CYP19A1 causes Aromatase excess syndrome (AEXS)
5579024 Defective MAT1A causes Methionine adenosyltransferase deficiency (MATD)
5579027 Defective CYP2R1 causes Rickets vitamin D-dependent 1B (VDDR1B)
5579026 Defective CYP11A1 causes Adrenal insufficiency, congenital, with 46,XY sex reversal (AICSR)
5579032 Defective TBXAS1 causes Ghosal hematodiaphyseal dysplasia (GHDD)
5579013 Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3)
5579012 Defective MAOA causes Brunner syndrome (BRUNS)
5579015 Defective CYP26B1 causes Radiohumeral fusions with other skeletal and craniofacial anomalies (RHFCA)
5579014 Defective CYP27B1 causes Rickets vitamin D-dependent 1A (VDDR1A)
5579009 Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency)
5579011 Defective CYP2U1 causes Spastic paraplegia 56, autosomal recessive (SPG56)
5579010 Defective CYP24A1 causes Hypercalcemia, infantile (HCAI)
5579021 Defective CYP21A2 causes Adrenal hyperplasia 3 (AH3)
5579020 Defective SLC35D1 causes Schneckenbecken dysplasia (SCHBCKD)
5579022 Defective GGT1 causes Glutathionuria (GLUTH)
5579017 Defective CYP11B1 causes Adrenal hyperplasia 4 (AH4)
5579016 Defective UGT1A4 causes hyperbilirubinemia
5579019 Defective FMO3 causes Trimethylaminuria (TMAU)
350864 Regulation of thyroid hormone activity
4549349 Defective ALG2 causes ALG2-CDG (CDG-1i)
4549356 Defective DPAGT1 causes DPAGT1-CDG (CDG-1j) and CMSTA2
4549380 Defective ALG1 causes ALG1-CDG (CDG-1k)
2453864 Retinoid cycle disease events
2453902 The canonical retinoid cycle in rods (twilight vision)
4551295 Defective ALG11 causes ALG11-CDG (CDG-1p)
5609975 Diseases associated with glycosylation precursor biosynthesis
5609974 Defective PGM1 causes PGM1-CDG (CDG1t)
5609977 Defective GALE can cause Epimerase-deficiency galactosemia (EDG)
5609976 Defective GALK1 can cause Galactosemia II (GALCT2)
5609978 Defective GALT can cause Galactosemia
2466712 Biosynthesis of A2E, implicated in retinal degradation
372790 Signaling by GPCR
373076 Class A/1 (Rhodopsin-like receptors)
373080 Class B/2 (Secretin family receptors)
375276 Peptide ligand-binding receptors
375281 Hormone ligand-binding receptors
375280 Amine ligand-binding receptors
5619037 Defective SLC35A1 causes congenital disorder of glycosylation 2F (CDG2F)
5619036 Defective SLC24A5 causes oculocutaneous albinism 6 (OCA6)
5619039 Defective SLC12A6 causes agenesis of the corpus callosum, with peripheral neuropathy (ACCPN)
5619035 Defective SLC17A5 causes Salla disease (SD) and ISSD
5619061 Defective SLC33A1 causes spastic paraplegia 42 (SPG42)
5619060 Defective CP causes aceruloplasminemia (ACERULOP)
5619063 Defective SLC29A3 causes histiocytosis-lymphadenopathy plus syndrome (HLAS)
5619062 Defective SLC1A3 causes episodic ataxia 6 (EA6)
5619056 Defective HK1 causes hexokinase deficiency (HK deficiency)
5619058 Defective SLCO1B3 causes hyperbilirubinemia, Rotor type (HBLRR)
5619068 Defective SLC2A10 causes arterial tortuosity syndrome (ATS)
5619071 Defective SLC22A12 causes renal hypouricemia 1 (RHUC1)
5619070 Defective SLC16A1 causes symptomatic deficiency in lactate transport (SDLT)
5619067 Defective SLC1A1 is implicated in schizophrenia 18 (SCZD18) and dicarboxylic aminoaciduria (DCBXA)
5619066 Defective SLC22A18 causes lung cancer (LNCR) and embryonal rhabdomyosarcoma 1 (RMSE1)
5619045 Defective SLC34A2 causes pulmonary alveolar microlithiasis (PALM)
5619044 Defective SLC6A19 causes Hartnup disorder (HND)
5619047 Defective SLC2A9 causes hypouricemia renal 2 (RHUC2)
5619046 Defective SLC26A4 causes Pendred syndrome (PDS)
5619041 Defective SLC36A2 causes iminoglycinuria (IG) and hyperglycinuria (HG)
5619040 Defective SLC34A1 causes hypophosphatemic nephrolithiasis/osteoporosis 1 (NPHLOP1)
5619043 Defective SLC2A1 causes GLUT1 deficiency syndrome 1 (GLUT1DS1)
5619042 Defective RHAG causes regulator type Rh-null hemolytic anemia (RHN)
5619053 Defective SLC22A5 causes systemic primary carnitine deficiency (CDSP)
5619052 Defective SLC9A9 causes autism 16 (AUTS16)
5619055 Defective SLC24A4 causes hypomineralized amelogenesis imperfecta (AI)
5619054 Defective SLC4A4 causes renal tubular acidosis, proximal, with ocular abnormalities and mental retardation (pRTA-OA)
5619049 Defective SLC40A1 causes hemochromatosis 4 (HFE4) (macrophages)
5619048 Defective SLC11A2 causes hypochromic microcytic anemia, with iron overload 1 (AHMIO1)
5619050 Defective SLC4A1 causes hereditary spherocytosis type 4 (HSP4), distal renal tubular acidosis (dRTA) and dRTA with hemolytic anemia (dRTA-HA)
4570571 Defective RFT1 causes RFT1-CDG (CDG-1n)
5619092 Defective SLC9A6 causes X-linked, syndromic mental retardation,, Christianson type (MRXSCH)
5619095 Defective SLCO2A1 causes primary, autosomal recessive hypertrophic osteoarthropathy 2 (PHOAR2)
5619094 Variant SLC6A14 may confer susceptibility towards obesity
5619089 Defective SLC6A5 causes hyperekplexia 3 (HKPX3)
5619088 Defective SLC39A4 causes acrodermatitis enteropathica, zinc-deficiency type (AEZ)
5619101 Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG)
5619102 SLC transporter disorders
5619097 Defective SLC34A3 causes Hereditary hypophosphatemic rickets with hypercalciuria (HHRH)
5619096 Defective SLC5A5 causes thyroid dyshormonogenesis 1 (TDH1)
5619099 Defective AVP causes neurohypophyseal diabetes insipidus (NDI)
5619098 Defective SLC2A2 causes Fanconi-Bickel syndrome (FBS)
5619077 Defective SLC24A1 causes congenital stationary night blindness 1D (CSNB1D)
5619076 Defective SLC17A8 causes autosomal dominant deafness 25 (DFNA25)
5619079 Defective SLC6A18 may confer susceptibility to iminoglycinuria and/or hyperglycinuria
5619078 Defective SLC35C1 causes congenital disorder of glycosylation 2C (CDG2C)
5619073 Defective GCK causes maturity-onset diabetes of the young 2 (MODY2)
5619072 Defective SLC35A2 causes congenital disorder of glycosylation 2M (CDG2M)
5619085 Defective SLC26A3 causes congenital secretory chloride diarrhea 1 (DIAR1)
5619084 ABC transporter disorders
5619087 Defective SLC12A3 causes Gitelman syndrome (GS)
5619081 Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)
5619083 Defective SLC35A3 causes arthrogryposis, mental retardation, and seizures (AMRS)
5619109 Defective SLC6A2 causes orthostatic intolerance (OI)
5619108 Defective SLC27A4 causes ichthyosis prematurity syndrome (IPS)
5619111 Defective SLC20A2 causes idiopathic basal ganglia calcification 1 (IBGC1)
5619110 Defective SLCO1B1 causes hyperbilirubinemia, Rotor type (HBLRR)
5619104 Defective SLC12A1 causes Bartter syndrome 1 (BS1)
5619107 Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC)
5619113 Defective SLC3A1 causes cystinuria (CSNU)
5619115 Disorders of transmembrane transporters
5619114 Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A)
2474795 Diseases associated with visual transduction
380095 Tachykinin receptors bind tachykinins
380108 Chemokine receptors bind chemokines
2485179 Activation of the phototransduction cascade
388479 Vasopressin-like receptors
389397 Orexin and neuropeptides FF and QRFP bind to their respective receptors
5633231 Defective ALG14 causes congenital myasthenic syndrome (ALG14-CMS)
390648 Muscarinic acetylcholine receptors
390651 Dopamine receptors
390650 Histamine receptors
390666 Serotonin receptors
390696 Adrenoceptors
391903 Eicosanoid ligand-binding receptors
391908 Prostanoid ligand receptors
391906 Leukotriene receptors
392170 ADP signalling through P2Y purinoceptor 12
5655799 Defective SLC40A1 causes hemochromatosis 4 (HFE4) (duodenum)
5656364 Defective SLC5A1 causes congenital glucose/galactose malabsorption (GGM)
3560801 Defective B3GAT3 causes JDSSDHD
3560796 Defective PAPSS2 causes SEMD-PA
3560792 Defective SLC26A2 causes chondrodysplasias
3560782 Diseases associated with glycosaminoglycan metabolism
3560783 Defective B4GALT7 causes EDS, progeroid type
5658208 Defective SLC5A2 causes renal glucosuria (GLYS1)
5658471 Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A)
5659735 Defective SLC6A19 causes Hartnup disorder (HND)
5659729 Defective SLC6A18 may confer susceptibility to iminoglycinuria and/or hyperglycinuria
2514859 Inactivation, recovery and regulation of the phototransduction cascade
2514856 The phototransduction cascade
5660686 Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG)
5660724 Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)
5660883 Defective SLC7A9 causes cystinuria (CSNU)
417957 P2Y receptors
417973 Adenosine P1 receptors
5660862 Defective SLC7A7 causes lysinuric protein intolerance (LPI)
418038 Nucleotide-like (purinergic) receptors
5661182 Defective SLCO1B1 causes hyperbilirubinemia, Rotor type (HBLRR)
419408 Lysosphingolipid and LPA receptors
419771 Opsins
419812 Calcitonin-like ligand receptors
420092 Glucagon-type ligand receptors
5663020 Defective SLC35A1 causes congenital disorder of glycosylation 2F (CDG2F)
420499 Class C/3 (Metabotropic glutamate/pheromone receptors)
425366 Transport of bile salts and organic acids, metal ions and amine compounds
425374 Amino acid and oligopeptide SLC transporters
425381 Bicarbonate transporters
425397 Transport of vitamins, nucleosides, and related molecules
425393 Transport of inorganic cations/anions and amino acids/oligopeptides
425407 SLC-mediated transmembrane transport
425410 Metal ion SLC transporters
425428 Amine compound SLC transporters
425471 Bile salt and organic anion SLC transporters
425561 Sodium/Calcium exchangers
1474151 Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation
425986 Sodium/Proton exchangers
426117 Cation-coupled Chloride cotransporters
5669034 TNFs bind their physiological receptors
427589 Type II Na+/Pi cotransporters
427601 Multifunctional anion exchangers
427652 Sodium-coupled phosphate cotransporters
427975 Proton/oligopeptide cotransporters
428559 Proton-coupled neutral amino acid transporters
428643 Organic anion transporters
429593 Inositol transporters
433137 Sodium-coupled sulphate, di- and tri-carboxylate transporters
433692 Proton-coupled monocarboxylate transport
435354 Zinc transporters
435368 Zinc efflux and compartmentalization by the SLC30 family
5678420 Defective ABCC9 causes dilated cardiomyopathy 10, familial atrial fibrillation 12 and hypertrichotic osteochondrodysplasia
5678520 Defective ABCB11 causes progressive familial intrahepatic cholestasis 2 and benign recurrent intrahepatic cholestasis 2
5678771 Defective ABCB4 causes progressive familial intrahepatic cholestasis 3, intrahepatic cholestasis of pregnancy 3 and gallbladder disease 1
5678895 Defective CFTR causes cystic fibrosis
5679090 Defective ABCG8 causes gallbladder disease 4 and sitosterolemia
5679096 Defective ABCG5 causes sitosterolemia
5679001 Defective ABCC2 causes Dubin-Johnson syndrome
5682113 Defective ABCA1 causes Tangier disease
5682294 Defective ABCA12 causes autosomal recessive congenital ichthyosis type 4B
5683177 Defective ABCC8 can cause hypoglycemias and hyperglycemias
5683329 Defective ABCD4 causes methylmalonic aciduria and homocystinuria, cblj type (MAHCJ)
5683371 Defective ABCB6 causes isolated colobomatous microphthalmia 7 (MCOPCB7)
5683678 Defective ABCA3 causes pulmonary surfactant metabolism dysfunction type 3 (SMDP3)
5683826 Surfactant metabolism
5684045 Defective ABCD1 causes adrenoleukodystrophy (ALD)
442380 Zinc influx into cells by the SLC39 gene family
442660 Na+/Cl- dependent neurotransmitter transporters
444411 Rhesus glycoproteins mediate ammonium transport.
5687583 Defective SLC34A2 causes pulmonary alveolar microlithiasis (PALM)
5687613 Diseases associated with surfactant metabolism
5687868 Defective SFTPA2 causes idiopathic pulmonary fibrosis (IPF)
5688031 Defective pro-SFTPB causes pulmonary surfactant metabolism dysfunction 1 (SMDP1) and respiratory distress syndrome (RDS)
5688399 Defective ABCA3 causes pulmonary surfactant metabolism dysfunction 3 (SMDP3)
5688354 Defective pro-SFTPC causes pulmonary surfactant metabolism dysfunction 2 (SMDP2) and respiratory distress syndrome (RDS)
5688849 Defective CSF2RB causes pulmonary surfactant metabolism dysfunction 5 (SMDP5)
5688890 Defective CSF2RA causes pulmonary surfactant metabolism dysfunction 4 (SMDP4)
5690338 Defective ABCC6 causes pseudoxanthoma elasticum (PXE)
3595174 Defective CHST14 causes EDS, musculocontractural type
3595172 Defective CHST3 causes SEDCJD
3595177 Defective CHSY1 causes TPBS
8849175 Threonine catabolism
8852405 Signaling by MST1
8853383 Lysosomal oligosaccharide catabolism
8866376 Reelin signalling pathway
8866423 VLDL assembly
8866427 VLDLR internalisation and degradation
8877627 Vitamin E
6783984 Glycine degradation
4687000 Defective MPDU1 causes MPDU1-CDG (CDG-1f)
6787639 GDP-fucose biosynthesis
6788656 Histidine, lysine, phenylalanine, tyrosine, proline and tryptophan catabolism
500792 GPCR ligand binding
6798163 Choline catabolism
6799198 Complex I biogenesis
3656244 Defective B4GALT1 causes B4GALT1-CDG (CDG-2d)
3656243 Defective ST3GAL3 causes MCT12 and EIEE15
3656253 Defective EXT1 causes exostoses 1, TRPS2 and CHDS
3656225 Defective CHST6 causes MCDC1
3656237 Defective EXT2 causes exostoses 2
6809583 Retinoid metabolism disease events
4717374 Defective DPM1 causes DPM1-CDG (CDG-1e)
4719360 Defective DPM3 causes DPM3-CDG (CDG-1o)
4719377 Defective DPM2 causes DPM2-CDG (CDG-1u)
4720454 Defective ALG9 causes ALG9-CDG (CDG-1l)
4720475 Defective ALG3 causes ALG3-CDG (CDG-1d)
4720489 Defective ALG12 causes ALG12-CDG (CDG-1g)
4724289 Defective ALG6 causes ALG6-CDG (CDG-1c)
4724325 Defective ALG8 causes ALG8-CDG (CDG-1h)
8935690 Digestion
8937144 Aryl hydrocarbon receptor signalling
549132 Organic cation/anion/zwitterion transport
549127 Organic cation transport
8942233 Intestinal infectious diseases
556833 Metabolism of lipids
561048 Organic anion transport
4755579 Defective SRD5A3 causes SRD5A3-CDG (CDG-1q) and KHRZ
4755583 Defective DOLK causes DOLK-CDG (CDG-1m)
4755609 Defective DHDDS causes retinitis pigmentosa 59
8956319 Nucleobase catabolism
8956320 Nucleobase biosynthesis
8956321 Nucleotide salvage
8957322 Metabolism of steroids
8963743 Digestion and absorption
2672351 Stimuli-sensing channels
8964043 Plasma lipoprotein clearance
8964046 VLDL clearance
8963889 Assembly of active LPL and LIPC lipase complexes
8964572 Lipid particle organization
1630316 Glycosaminoglycan metabolism
1638074 Keratan sulfate/keratin metabolism
1638091 Heparan sulfate/heparin (HS-GAG) metabolism
8978868 Fatty acid metabolism
8979227 Triglyceride metabolism
4793950 Defective MAN1B1 causes MRT15
4793953 Defective B4GALT1 causes B4GALT1-CDG (CDG-2d)
4793952 Defective MGAT2 causes MGAT2-CDG (CDG-2a)
4793954 Defective MOGS causes MOGS-CDG (CDG-2b)
611105 Respiratory electron transport
1660662 Glycosphingolipid metabolism
1663150 The activation of arylsulfatases
3781865 Diseases of glycosylation
3781860 Diseases associated with N-glycosylation of proteins
727802 Transport of nucleotide sugars
1793185 Chondroitin sulfate/dermatan sulfate metabolism
3906995 Diseases associated with O-glycosylation of proteins
804914 Transport of fatty acids
1912420 Pre-NOTCH Processing in Golgi
879518 Transport of organic anions
881907 Gastrin-CREB signalling pathway via PKC and MAPK
5083629 Defective POMT2 causes MDDGA2, MDDGB2 and MDDGC2
5083628 Defective POMGNT1 causes MDDGA3, MDDGB3 and MDDGC3
5083630 Defective LFNG causes SCDO3
5083625 Defective GALNT3 causes familial hyperphosphatemic tumoral calcinosis (HFTC)
5083627 Defective LARGE causes MDDGA6 and MDDGB6
5083636 Defective GALNT12 causes colorectal cancer 1 (CRCS1)
5083633 Defective POMT1 causes MDDGA1, MDDGB1 and MDDGC1
5083632 Defective C1GALT1C1 causes Tn polyagglutination syndrome (TNPS)
5083635 Defective B3GALTL causes Peters-plus syndrome (PpS)
4043916 Defective MPI causes MPI-CDG (CDG-1b)
4043911 Defective PMM2 causes PMM2-CDG (CDG-1a)
913709 O-linked glycosylation of mucins
1971475 A tetrasaccharide linker sequence is required for GAG synthesis
1980150 Signaling by NOTCH4
1980148 Signaling by NOTCH3
1980145 Signaling by NOTCH2
936837 Ion transport by P-type ATPases
4085023 Defective GFPT1 causes CMSTA1
4085011 Defective GNE causes sialuria, Nonaka myopathy and inclusion body myopathy 2
4085001 Sialic acid metabolism
2022870 Chondroitin sulfate biosynthesis
2022857 Keratan sulfate degradation
2022854 Keratan sulfate biosynthesis
2022928 HS-GAG biosynthesis
2022923 Dermatan sulfate biosynthesis
2024101 CS/DS degradation
2024096 HS-GAG degradation
975634 Retinoid metabolism and transport
977068 Termination of O-glycan biosynthesis
5173105 O-linked glycosylation
5173214 O-glycosylation of TSR domain-containing proteins
983712 Ion channel transport
5223345 Miscellaneous transport and binding events

Pathways reviewed by Jassal, Bijay (73447)

DB_ID Name
5252538 Drosophila signaling pathways
2160456 Phenylketonuria
2161517 Abacavir transmembrane transport
2161522 Abacavir transport and metabolism
2161541 Abacavir metabolism
70350 Fructose catabolism
75109 Triglyceride biosynthesis
75896 Plasmalogen biosynthesis
3229121 Glycogen storage diseases
3229133 Glycogen storage disease type Ib (SLC37A4)
5357572 Lysosomal glycogen catabolism
5357609 Glycogen storage disease type II (GAA)
3274531 Glycogen storage disease type Ia (G6PC)
3282872 Severe congenital neutropenia type 4 (G6PC3)
163560 Triglyceride catabolism
174824 Plasma lipoprotein assembly, remodeling, and clearance
3322077 Glycogen synthesis
1237044 Erythrocytes take up carbon dioxide and release oxygen
191273 Cholesterol biosynthesis
1247673 Erythrocytes take up oxygen and release carbon dioxide
204626 Hypusine synthesis from eIF5A-lysine
1296025 ATP sensitive Potassium channels
1296053 Classical Kir channels
1296052 Ca2+ activated K+ channels
1296059 G protein gated Potassium channels
1296061 HCN channels
1296041 Activation of G protein gated Potassium channels
1296067 Potassium transport channels
1296065 Inwardly rectifying K+ channels
1296071 Potassium Channels
1296072 Voltage gated Potassium channels
1296346 Tandem pore domain potassium channels
1299287 Tandem pore domain halothane-inhibited K+ channel (THIK)
1299316 TWIK-releated acid-sensitive K+ channel (TASK)
1299308 Tandem of pore domain in a weak inwardly rectifying K+ channels (TWIK)
1299344 TWIK-related spinal cord K+ channel (TRESK)
1299361 TWIK-related alkaline pH activated K+ channel (TALK)
1299503 TWIK related potassium channel (TREK)
352230 Amino acid transport across the plasma membrane
382551 Transport of small molecules
389542 NADPH regeneration
389599 Alpha-oxidation of phytanate
389661 Glyoxylate metabolism and glycine degradation
389887 Beta-oxidation of pristanoyl-CoA
390247 Beta-oxidation of very long chain fatty acids
390918 Peroxisomal lipid metabolism
5652227 Fructose biosynthesis
5653890 Lactose synthesis
5657562 Essential fructosuria
5657560 Hereditary fructose intolerance
5659898 Intestinal saccharidase deficiencies
5659996 RPIA deficiency: failed conversion of R5P to RU5P
5661270 Catabolism of glucuronate to xylulose-5-phosphate
5662853 Essential pentosuria
1475029 Reversible hydration of carbon dioxide
428157 Sphingolipid metabolism
1480926 O2/CO2 exchange in erythrocytes
8848584 Wax biosynthesis
6791055 TALDO1 deficiency: failed conversion of SH7P, GA3P to Fru(6)P, E4P
6791462 TALDO1 deficiency: failed conversion of Fru(6)P, E4P to SH7P, GA3P
6791461 RPIA deficiency: failed conversion of RU5P to R5P
6791465 Pentose phosphate pathway disease
6806667 Metabolism of fat-soluble vitamins
6806664 Metabolism of vitamin K
6807047 Cholesterol biosynthesis via desmosterol
6807062 Cholesterol biosynthesis via lathosterol
6814848 Glycerophospholipid catabolism
8955332 Carboxyterminal post-translational modifications of tubulin
8957322 Metabolism of steroids
8963676 Intestinal absorption
8963678 Intestinal lipid absorption
8964011 HDL clearance
8964026 Chylomicron clearance
8964041 LDL remodeling
8964043 Plasma lipoprotein clearance
8964038 LDL clearance
8964058 HDL remodeling
8963896 HDL assembly
8963898 Plasma lipoprotein assembly
8963899 Plasma lipoprotein remodeling
8963901 Chylomicron remodeling
8963888 Chylomicron assembly
8978868 Fatty acid metabolism
8978934 Metabolism of cofactors
8979227 Triglyceride metabolism
8982491 Glycogen metabolism
3814836 Glycogen storage disease type XV (GYG1)
3828062 Glycogen storage disease type 0 (muscle GYS1)
3858516 Glycogen storage disease type 0 (liver GYS2)
3878781 Glycogen storage disease type IV (GBE1)
880009 Interconversion of 2-oxoglutarate and 2-hydroxyglutarate
2978092 Abnormal conversion of 2-oxoglutarate to 2-hydroxyglutarate

Details on Person Jassal, Bijay

Class:IdPerson:73447
_displayNameJassal, Bijay
_timestamp2017-08-22 20:36:49
affiliation[Affiliation:70170] EBI
crossReference[DatabaseIdentifier:5357567] ORCID:0000-0002-5039-5405
firstnameBijay
initialB
modified[InstanceEdit:158705] D'Eustachio, P, 2005-02-05 20:20:55
[InstanceEdit:158817] D'Eustachio, P, 2005-02-09 01:29:48
[InstanceEdit:158841] D'Eustachio, P, 2005-02-09 14:55:43
[InstanceEdit:158897] D'Eustachio, P, 2005-02-10 21:54:22
[InstanceEdit:5357566] Jassal, Bijay, 2014-03-24
surnameJassal
(author)[LiteratureReference:5612460] A controlled vocabulary for pathway entities and events
[InstanceEdit:73446] Jassal, B, 2003-06-17 09:00:25
[InstanceEdit:73449] Jassal, B, 2003-06-17 09:00:26
[InstanceEdit:73784] Jassal, B, 2003-06-26 04:06:16
[InstanceEdit:73832] Jassal, B, 2003-07-03 08:48:35
[InstanceEdit:74183] Jassal, B, 2003-07-17 08:31:43
[InstanceEdit:76326] Jassal, B, 2003-08-05 00:00:00
[InstanceEdit:76554] Jassal, B, 2003-10-10 05:22:25
[InstanceEdit:111280] Jassal, B, 2004-02-11 10:27:31
[InstanceEdit:111668] Jassal, B, 2004-03-10 10:57:21
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