Species

KNApSAcK Entry

Organism name Heracleum candicans WALL.
Genus Heracleum
Family Apiaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Heracleum
Linked NCBI taxonomy ID 40917
Linked level genus

Family

Family in NCBI taxonomy Apiaceae
ID 4037

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (21)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
KCF-S
cluster
phytochemical
cluster
figure
C00029680 External link 512 Ammajin
/ Marmesinin
/ (-)-Marmesinin
CHEMBL459825
11 / 8 / 6 No. 399 No. 25
C00002488 External link 512 Osthol
/ Osthole
CHEMBL52229
C046627
12 / 6 / 5 7 / 4 No. 466 No. 25
C00029597 External link 512 8-(3-Chloro-2-hydroxy-3-methylbutoxy)psoralen
/ (+)-8-(3-Chloro-2-hydroxy-3-methylbutoxy)psoralen
No. 579 No. 25
C00030531 External link 512 Isogosferol
/ Isogospherol
/ (+)-Isogospherol
No. 606 No. 25
C00002493 External link 512 Pimpinellin
CHEMBL1491809
C039409
3 / 0 / 1 No. 606 No. 25
C00031177 External link 512 Rivulobirin C
No. 692
C00031178 External link 512 Rivulobirin D
/ (-)-Rivulobirin D
No. 692
C00029608 External link 512 9,17-Octadecadiene-12,14-diyne-1,11,16-triol
No. 940 No. 69
C00001283 External link 512 Falcarindiol
CHEMBL69018
CHEMBL1094112
C034379
3 / 0 / 0 No. 940 No. 69
C00002503 External link 512 Umbelliferon
/ Umbelliferone
/ 7-Hydroxycoumarin
CHEMBL51628
C031477
39 / 33 / 32 9 / 0 No. 1030 No. 25
C00000584 External link 512 (+)-Marmesin
CHEMBL442813
CHEMBL1464240
C001684
12 / 24 / 49 No. 1336 No. 25
C00029297 External link 512 Columbianetin
/ (+)-Columbianetin
CHEMBL201152
7 / 12 / 8 No. 1336 No. 25
C00029602 External link 512 8-Geranyl-5-methoxypsoralen
/ 8-Geranyloxy-5-methoxypsoralen
CHEMBL1934197
1 / 0 / 0 No. 1664
C00030973 External link 512 Peucedanol
No. 1726
C00029304 External link 512 (+)-Meranzin hydrate
CHEMBL433093
2 / 0 / 0 No. 1726
C00030900 External link 512 Osthenol
CHEMBL350475
C114745
2 / 0 / 0 No. 2087
C00031176 External link 512 Rivulobirin A
CHEMBL1731549
3 / 1 / 1 No. 2316
C00031179 External link 512 Rivulobirin E
No. 2316
C00031181 External link 512 Rivulotririn B
No. 5571
C00031180 External link 512 Rivulotririn A
No. 5571
C00031079 External link 512 Prandiol
/ Protangix
CHEMBL932
D004176
174 / 113 / 83 33 / 77 No. 8896

Human Protein / Gene in interactions

209 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P00352 Retinal dehydrogenase 1 Enzyme C00002488 C00002493 C00002503 C00029297 C00029680 C00031079 0 / 0
P56817 Beta-secretase 1 A1A C00000584 C00002488 C00002503 C00029297 C00029602 C00030900 0 / 0
O75496 Geminin Unclassified protein C00002488 C00002503 C00029680 C00031079 C00031176 0 / 0
P17405 Sphingomyelin phosphodiesterase Enzyme C00000584 C00029297 C00029680 C00031079 2 / 2
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00001283 C00002488 C00030900 C00031079 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002503 C00029297 C00029304 C00031079 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00002503 C00029297 C00029680 C00031079 1 / 1
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002503 C00029297 C00029680 C00031079 2 / 2
P22303 Acetylcholinesterase Hydrolase C00000584 C00002503 C00029680 C00031079 1 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00000584 C00031079 C00031176 0 / 0
Q99700 Ataxin-2 Unclassified protein C00002503 C00031079 C00031176 1 / 1
P04062 Glucosylceramidase Enzyme C00000584 C00002488 C00002503 6 / 4
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002488 C00002493 C00031079 0 / 1
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00000584 C00029680 C00031079 1 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00002488 C00002503 C00029304 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00002488 C00031079 0 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00002503 C00031079 0 / 3
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002503 C00031079 1 / 2
P38398 Breast cancer type 1 susceptibility protein Enzyme C00000584 C00031079 4 / 2
P06280 Alpha-galactosidase A Enzyme C00002503 C00029680 1 / 1
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00002503 C00031079 3 / 3
P55210 Caspase-7 C14 C00002503 C00031079 0 / 0
P29466 Caspase-1 C14 C00002503 C00031079 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00002503 C00031079 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00000584 C00029680 0 / 0
P04406 Glyceraldehyde-3-phosphate dehydrogenase Enzyme C00002488 C00002503 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00029680 C00031079 0 / 0
P41145 Kappa-type opioid receptor Opioid receptor C00001283 C00031079 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00002503 C00031079 1 / 1
O00255 Menin Unclassified protein C00002503 C00031079 2 / 5
P00918 Carbonic anhydrase 2 Lyase C00002503 C00031079 1 / 2
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00031079 1 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00031079 3 / 2
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00002503 1 / 1
Q99808 Equilibrative nucleoside transporter 1 Nucleoside uniporter C00031079 0 / 0
P10828 Thyroid hormone receptor beta NR1A2 C00031079 3 / 1
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00031079 0 / 0
P07550 Beta-2 adrenergic receptor Adrenergic receptor C00031079 0 / 1
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00031079 1 / 1
P25021 Histamine H2 receptor Histamine receptor C00031079 0 / 0
P35367 Histamine H1 receptor Histamine receptor C00031079 0 / 0
Q01959 Sodium-dependent dopamine transporter Dopamine C00031079 1 / 0
P08912 Muscarinic acetylcholine receptor M5 Acetylcholine receptor C00031079 0 / 0
P18825 Alpha-2C adrenergic receptor Adrenergic receptor C00031079 0 / 0
P13945 Beta-3 adrenergic receptor Adrenergic receptor C00031079 0 / 0
P34969 5-hydroxytryptamine receptor 7 Serotonin receptor C00001283 0 / 0
P08183 Multidrug resistance protein 1 drug C00031079 1 / 0
P25024 C-X-C chemokine receptor type 1 CXC chemokine receptor C00031079 0 / 0
P06241 Tyrosine-protein kinase Fyn Src C00031079 0 / 0
Q08209 Serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform Ser_Thr C00031079 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00031079 0 / 1
O95263 High affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8B PDE_8B C00031079 2 / 1
P54132 Bloom syndrome protein Enzyme C00031079 1 / 2
O15245 Solute carrier family 22 member 1 Drug uniporter C00031079 0 / 0
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00031079 1 / 8
P14416 D(2) dopamine receptor Dopamine receptor C00031079 2 / 0
Q13315 Serine-protein kinase ATM Atypical serine/threonine protein kinase PIKK subfamily C00031079 1 / 4
P37288 Vasopressin V1a receptor Vasopressin and oxytocin receptor C00031079 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00031079 0 / 0
Q9Y271 Cysteinyl leukotriene receptor 1 Leukotriene receptor C00031079 0 / 0
P29274 Adenosine receptor A2a Adenosine receptor C00031079 0 / 0
P25929 Neuropeptide Y receptor type 1 Neuropeptide Y receptor C00031079 0 / 0
P50052 Type-2 angiotensin II receptor Angiotensin receptor C00031079 1 / 1
O15296 Arachidonate 15-lipoxygenase B Enzyme C00031079 0 / 0
P17948 Vascular endothelial growth factor receptor 1 Vegfr C00031079 0 / 0
P41968 Melanocortin receptor 3 Melanocortin receptor C00031079 1 / 0
P14780 Matrix metalloproteinase-9 M10A C00031079 2 / 2
P28845 Corticosteroid 11-beta-dehydrogenase isozyme 1 Enzyme C00002503 1 / 1
P27361 Mitogen-activated protein kinase 3 Erk C00031079 0 / 0
O43570 Carbonic anhydrase 12 Lyase C00002503 1 / 2
P11509 Cytochrome P450 2A6 Cytochrome P450 2A6 C00031079 0 / 0
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00031079 0 / 0
O60658 High affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8A PDE_8A C00031079 0 / 0
P39748 Flap endonuclease 1 Enzyme C00002503 0 / 0
P17252 Protein kinase C alpha type Alpha C00031079 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00031079 2 / 0
P49146 Neuropeptide Y receptor type 2 Neuropeptide Y receptor C00031079 0 / 0
O15439 Multidrug resistance-associated protein 4 Unclassified protein C00031079 0 / 0
Q16539 Mitogen-activated protein kinase 14 p38 C00031079 0 / 0
P54855 UDP-glucuronosyltransferase 2B15 Enzyme C00002503 0 / 0
P04035 3-hydroxy-3-methylglutaryl-coenzyme A reductase Oxidoreductase C00031079 0 / 0
P08913 Alpha-2A adrenergic receptor Adrenergic receptor C00031079 0 / 0
P18405 3-oxo-5-alpha-steroid 4-dehydrogenase 1 Oxidoreductase C00002503 0 / 0
P21917 D(4) dopamine receptor Dopamine receptor C00031079 0 / 0
P30988 Calcitonin receptor Calcitonin receptor C00031079 0 / 0
P35462 D(3) dopamine receptor Dopamine receptor C00031079 1 / 0
P41143 Delta-type opioid receptor Opioid receptor C00031079 0 / 0
Q92731 Estrogen receptor beta NR3A2 C00031079 0 / 1
P41595 5-hydroxytryptamine receptor 2B Serotonin receptor C00031079 0 / 0
P15121 Aldose reductase Enzyme C00002503 0 / 0
P25101 Endothelin-1 receptor Endothelin receptor C00031079 0 / 0
P30411 B2 bradykinin receptor Bradykinin receptor C00031079 0 / 0
P32245 Melanocortin receptor 4 Melanocortin receptor C00031079 1 / 0
P00915 Carbonic anhydrase 1 Lyase C00002503 0 / 0
P32238 Cholecystokinin receptor type A Cholecystokinin receptor C00031079 0 / 0
P08311 Cathepsin G S1A C00031079 0 / 0
Q99720 Sigma non-opioid intracellular receptor 1 Membrane receptor C00031079 1 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00002488 0 / 0
P03956 Interstitial collagenase M10A C00031079 0 / 1
P32241 Vasoactive intestinal polypeptide receptor 1 Vasoactive intestinal peptide receptor C00031079 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00029297 7 / 3
Q9Y233 cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A PDE_10A C00031079 0 / 0
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00029680 0 / 0
P33765 Adenosine receptor A3 Adenosine receptor C00031079 0 / 0
P08246 Neutrophil elastase S1A C00031079 2 / 1
Q9NPD5 Solute carrier organic anion transporter family member 1B3 Electrochemical transporter C00031079 1 / 0
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00031079 2 / 2
Q99816 Tumor susceptibility gene 101 protein Unclassified protein C00031079 0 / 0
P04150 Glucocorticoid receptor NR3C1 C00031079 0 / 1
P08172 Muscarinic acetylcholine receptor M2 Acetylcholine receptor C00031079 2 / 0
P11229 Muscarinic acetylcholine receptor M1 Acetylcholine receptor C00031079 0 / 0
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00000584 2 / 2
P14679 Tyrosinase Oxidoreductase C00002503 4 / 2
P21554 Cannabinoid receptor 1 Cannabinoid receptor C00031079 0 / 0
P31645 Sodium-dependent serotonin transporter Serotonin C00031079 2 / 0
P04626 Receptor tyrosine-protein kinase erbB-2 TK tyrosine-protein kinase EGFR subfamily C00031079 5 / 9
P20309 Muscarinic acetylcholine receptor M3 Acetylcholine receptor C00031079 1 / 0
P21452 Substance-K receptor Neurokinin receptor C00031079 0 / 0
P51679 C-C chemokine receptor type 4 CC chemokine receptor C00031079 0 / 0
P51681 C-C chemokine receptor type 5 CC chemokine receptor C00031079 3 / 0
P50406 5-hydroxytryptamine receptor 6 Serotonin receptor C00031079 0 / 0
P21728 D(1A) dopamine receptor Dopamine receptor C00031079 0 / 0
P41597 C-C chemokine receptor type 2 CC chemokine receptor C00031079 1 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00031079 0 / 0
P08575 Receptor-type tyrosine-protein phosphatase C Enzyme C00031079 2 / 1
P09917 Arachidonate 5-lipoxygenase Oxidoreductase C00002488 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00031079 0 / 0
Q16790 Carbonic anhydrase 9 Lyase C00002503 0 / 1
P49798 Regulator of G-protein signaling 4 Unclassified protein C00031079 2 / 0
Q92887 Canalicular multispecific organic anion transporter 1 Unclassified protein C00031079 1 / 1
Q9HAW8 UDP-glucuronosyltransferase 1-10 Enzyme C00002503 0 / 0
O15118 Niemann-Pick C1 protein Unclassified protein C00000584 1 / 1
Q01453 Peripheral myelin protein 22 Unclassified protein C00031079 5 / 2
Q96FL8 Multidrug and toxin extrusion protein 1 Cation antiporter C00031079 0 / 0
Q86VL8 Multidrug and toxin extrusion protein 2 Cation antiporter C00031079 0 / 0
Q9HAW9 UDP-glucuronosyltransferase 1-8 Enzyme C00002503 0 / 0
Q9Y4X1 UDP-glucuronosyltransferase 2A1 Enzyme C00002503 0 / 0
O76074 cGMP-specific 3',5'-cyclic phosphodiesterase PDE_5A C00031079 0 / 0
P03372 Estrogen receptor NR3A1 C00031079 1 / 1
P08588 Beta-1 adrenergic receptor Adrenergic receptor C00031079 1 / 0
O94956 Solute carrier organic anion transporter family member 2B1 Unclassified protein C00031079 0 / 0
P28223 5-hydroxytryptamine receptor 2A Serotonin receptor C00031079 0 / 0
P28335 5-hydroxytryptamine receptor 2C Serotonin receptor C00031079 0 / 0
P35372 Mu-type opioid receptor Opioid receptor C00031079 0 / 0
P08173 Muscarinic acetylcholine receptor M4 Acetylcholine receptor C00031079 0 / 0
P25103 Substance-P receptor Neurokinin receptor C00031079 0 / 0
P25105 Platelet-activating factor receptor PAF receptor C00031079 0 / 0
P33032 Melanocortin receptor 5 Melanocortin receptor C00031079 0 / 0
Q00796 Sorbitol dehydrogenase Enzyme C00002503 0 / 0
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor C00031079 0 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme C00002493 0 / 0
O15244 Solute carrier family 22 member 2 Drug uniporter C00031079 0 / 0
Q9HCR9 Dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11A PDE_11A C00031079 1 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00031079 1 / 1
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00031079 0 / 0
P05181 Cytochrome P450 2E1 Cytochrome P450 2E1 C00031079 0 / 0
P02545 Prelamin-A/C Unclassified protein C00031079 11 / 10
Q6W5P4 Neuropeptide S receptor Neuropeptide receptor C00031079 1 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00031079 0 / 0
P22309 UDP-glucuronosyltransferase 1-1 Enzyme C00002503 5 / 1
P10636 Microtubule-associated protein tau Unclassified protein C00031079 4 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00031079 0 / 0
P10275 Androgen receptor NR3C4 C00031079 3 / 4
P23975 Sodium-dependent noradrenaline transporter Norepinephrine C00031079 1 / 1
P25100 Alpha-1D adrenergic receptor Adrenergic receptor C00031079 0 / 0
P30542 Adenosine receptor A1 Adenosine receptor C00031079 0 / 0
P18089 Alpha-2B adrenergic receptor Adrenergic receptor C00031079 0 / 0
P24557 Thromboxane-A synthase Cytochrome P450 5A1 C00031079 1 / 1
Q9NP56 cAMP-specific 3',5'-cyclic phosphodiesterase 7B PDE_7B C00031079 0 / 0
P06239 Tyrosine-protein kinase Lck Src C00031079 0 / 1
O00408 cGMP-dependent 3',5'-cyclic phosphodiesterase PDE_2A C00031079 0 / 0
P25025 C-X-C chemokine receptor type 2 CXC chemokine receptor C00031079 0 / 0
P80365 Corticosteroid 11-beta-dehydrogenase isozyme 2 Enzyme C00002503 1 / 1
O14980 Exportin-1 Unclassified protein C00002488 0 / 0
Q14145 Kelch-like ECH-associated protein 1 Unclassified protein C00031079 0 / 0
Q9Y6L6 Solute carrier organic anion transporter family member 1B1 Electrochemical transporter C00031079 1 / 0
P40225 Thrombopoietin Unclassified protein C00031079 1 / 1
O00167 Eyes absent homolog 2 Enzyme C00031079 0 / 0
Q16637 Survival motor neuron protein Unclassified protein C00031079 4 / 1
P04637 Cellular tumor antigen p53 Transcription Factor C00000584 7 / 37
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00031079 1 / 0
Q8IUX4 DNA dC->dU-editing enzyme APOBEC-3F Enzyme C00031079 0 / 0
O15440 Multidrug resistance-associated protein 5 Unclassified protein C00031079 0 / 0
P22310 UDP-glucuronosyltransferase 1-4 Enzyme C00002503 3 / 0
Q08493 cAMP-specific 3',5'-cyclic phosphodiesterase 4C PDE_4C C00031079 0 / 0
Q07343 cAMP-specific 3',5'-cyclic phosphodiesterase 4B PDE_4B C00031079 0 / 0
P27815 cAMP-specific 3',5'-cyclic phosphodiesterase 4A PDE_4A C00031079 0 / 0
Q08499 cAMP-specific 3',5'-cyclic phosphodiesterase 4D PDE_4D C00031079 1 / 0
P18545 Retinal rod rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit gamma PDE_6G C00031079 1 / 1
O43924 Retinal rod rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit delta PDE_6D C00031079 0 / 0
P51160 Cone cGMP-specific 3',5'-cyclic phosphodiesterase subunit alpha' PDE_6C C00031079 1 / 1
Q13956 Retinal cone rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit gamma PDE_6H C00031079 1 / 1
P16499 Rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit alpha PDE_6A C00031079 1 / 1
P35913 Rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit beta PDE_6B C00031079 2 / 2
Q86TP1 Protein prune homolog Enzyme C00031079 0 / 0
Q13370 cGMP-inhibited 3',5'-cyclic phosphodiesterase B PDE_3B C00031079 0 / 0
Q14432 cGMP-inhibited 3',5'-cyclic phosphodiesterase A PDE_3A C00031079 0 / 0
Q14123 Calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1C PDE_1C C00031079 0 / 0
P54750 Calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1A PDE_1A C00031079 0 / 0
Q01064 Calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1B PDE_1B C00031079 0 / 0
P07900 Heat shock protein HSP 90-alpha Other cytosolic protein C00031079 0 / 0
P08238 Heat shock protein HSP 90-beta Other cytosolic protein C00031079 0 / 0
Q9NY46 Sodium channel protein type 3 subunit alpha SCN alpha, NaV1.x C00031079 0 / 0
Q99250 Sodium channel protein type 2 subunit alpha SCN alpha, NaV1.x C00031079 2 / 2
P35498 Sodium channel protein type 1 subunit alpha SCN alpha, NaV1.x C00031079 3 / 2
Q13946 High affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A PDE_7A C00031079 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00002503 0 / 0
P01215 Glycoprotein hormones alpha chain Unclassified protein C00000584 0 / 3
Q13148 TAR DNA-binding protein 43 Unclassified protein C00031079 1 / 1

49 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
8644 AKR1C3, DD3, DDX, HA1753, HAKRB, HAKRe, HSD17B5, PGFS, hluPGFS aldo-keto reductase family 1, member C3 (EC:1.3.1.20 1.1.1.188 1.1.1.239 1.1.1.64 1.1.1.112 1.1.1.357) C00002503
8574 AKR7A2, AFAR, AFAR1, AFB1-AR1, AKR7 aldo-keto reductase family 7, member A2 (aflatoxin aldehyde reductase) (EC:1.1.1.n11) C00002503
581 BAX, BCL2L4 BCL2-associated X protein C00002503
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00002503
595 CCND1, BCL1, D11S287E, PRAD1, U21B31 cyclin D1 C00002503
1548 CYP2A6, CPA6, CYP2A, CYP2A3, CYPIIA6, P450C2A, P450PB cytochrome P450, family 2, subfamily A, polypeptide 6 (EC:1.14.14.1) C00002503
6817 SULT1A1, HAST1/HAST2, P-PST, PST, ST1A1, ST1A3, STP, STP1, TSPST1 sulfotransferase family, cytosolic, 1A, phenol-preferring, member 1 (EC:2.8.2.1) C00002503
54600 UGT1A9, HLUGP4, LUGP4, UDPGT, UDPGT_1-9, UGT-1I, UGT1-09, UGT1-9, UGT1.9, UGT1AI, UGT1I UDP glucuronosyltransferase 1 family, polypeptide A9 (EC:2.4.1.17) C00002503
7366 UGT2B15, HLUG4, UDPGT_2B8, UDPGT2B15, UDPGTH3, UGT2B8 UDP glucuronosyltransferase 2 family, polypeptide B15 (EC:2.4.1.17) C00002503
2180 ACSL1, ACS1, FACL1, FACL2, LACS, LACS1, LACS2 acyl-CoA synthetase long-chain family member 1 (EC:6.2.1.3) C00002488
1374 CPT1A, CPT1, CPT1-L, L-CPT1 carnitine palmitoyltransferase 1A (liver) (EC:2.3.1.21) C00002488
4313 MMP2, CLG4, CLG4A, MMP-II, MONA, TBE-1 matrix metallopeptidase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IV collagenase) (EC:3.4.24.24) C00002488
4318 MMP9, CLG4B, GELB, MANDP2, MMP-9 matrix metallopeptidase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase) (EC:3.4.24.35) C00002488
4792 NFKBIA, IKBA, MAD-3, NFKBI nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha C00002488
5465 PPARA, NR1C1, PPAR, PPARalpha, hPPAR peroxisome proliferator-activated receptor alpha C00002488
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00002488
10257 ABCC4, EST170205, MOAT-B, MOATB, MRP4 ATP-binding cassette, sub-family C (CFTR/MRP), member 4 C00031079
348 APOE, AD2, LDLCQ5, LPG apolipoprotein E C00031079
598 BCL2L1, BCL-XL/S, BCL2L, BCLX, BCLXL, BCLXS, Bcl-X, PPP1R52, bcl-xL, bcl-xS BCL2-like 1 C00031079
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00031079
840 CASP7, CASP-7, CMH-1, ICE-LAP3, LICE2, MCH3 caspase 7, apoptosis-related cysteine peptidase (EC:3.4.22.60) C00031079
841 CASP8, ALPS2B, CAP4, Casp-8, FLICE, MACH, MCH5 caspase 8, apoptosis-related cysteine peptidase (EC:3.4.22.61) C00031079
959 CD40LG, CD154, CD40L, HIGM1, IGM, IMD3, T-BAM, TNFSF5, TRAP, gp39, hCD40L CD40 ligand C00031079
8837 CFLAR, CASH, CASP8AP1, CLARP, Casper, FLAME, FLAME-1, FLAME1, FLIP, I-FLICE, MRIT, c-FLIP, c-FLIPL, c-FLIPR, c-FLIPS CASP8 and FADD-like apoptosis regulator C00031079
1277 COL1A1, OI4 collagen, type I, alpha 1 C00031079
1281 COL3A1, EDS4A collagen, type III, alpha 1 C00031079
56616 DIABLO, DFNA64, SMAC diablo, IAP-binding mitochondrial protein C00031079
8772 FADD, MORT1 Fas (TNFRSF6)-associated via death domain C00031079
2353 FOS, AP-1, C-FOS, p55 FBJ murine osteosarcoma viral oncogene homolog C00031079
3553 IL1B, IL-1, IL1-BETA, IL1F2 interleukin 1, beta C00031079
3643 INSR, CD220, HHF5 insulin receptor (EC:2.7.10.1) C00031079
5599 MAPK8, JNK, JNK-46, JNK1, JNK1A2, JNK21B1/2, PRKM8, SAPK1, SAPK1c mitogen-activated protein kinase 8 (EC:2.7.11.24) C00031079
4879 NPPB, BNP natriuretic peptide B C00031079
5004 ORM1, AGP-A, AGP1, ORM orosomucoid 1 C00031079
5005 ORM2, AGP-B, AGP-B', AGP2 orosomucoid 2 C00031079
10846 PDE10A, HSPDE10A phosphodiesterase 10A (EC:3.1.4.35 3.1.4.17) C00031079
50940 PDE11A, PPNAD2 phosphodiesterase 11A (EC:3.1.4.35 3.1.4.17) C00031079
8654 PDE5A, CGB-PDE, CN5A, PDE5 phosphodiesterase 5A, cGMP-specific (EC:3.1.4.35) C00031079
5150 PDE7A, HCP1, PDE7 phosphodiesterase 7A (EC:3.1.4.17) C00031079
27115 PDE7B, bA472E5.1 phosphodiesterase 7B (EC:3.1.4.17) C00031079
5151 PDE8A, HsT19550 phosphodiesterase 8A (EC:3.1.4.17) C00031079
8622 PDE8B, ADSD, PPNAD3 phosphodiesterase 8B (EC:3.1.4.17) C00031079
5327 PLAT, T-PA, TPA plasminogen activator, tissue (EC:3.4.21.68) C00031079
1827 RCAN1, ADAPT78, CSP1, DSC1, DSCR1, MCIP1, RCN1 regulator of calcineurin 1 C00031079
2030 SLC29A1, ENT1 solute carrier family 29 (equilibrative nucleoside transporter), member 1 C00031079
3177 SLC29A2, DER12, ENT2, HNP36 solute carrier family 29 (equilibrative nucleoside transporter), member 2 C00031079
6521 SLC4A1, AE1, BND3, CD233, DI, EMPB3, EPB3, FR, RTA1A, SW, WD, WD1, WR solute carrier family 4 (anion exchanger), member 1 C00031079
7040 TGFB1, CED, DPD1, LAP, TGFB, TGFbeta transforming growth factor, beta 1 C00031079
7422 VEGFA, MVCD1, VEGF, VPF vascular endothelial growth factor A C00031079

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (149)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#100100 Abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism P20309
#614613 Acrodysostosis 2, with or without hormone resistance; acrdys2 Q08499
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#103470 Albinism, ocular, with sensorineural deafness P14679
#203100 Albinism, oculocutaneous, type ia; oca1a P14679
#606952 Albinism, oculocutaneous, type ib; oca1b P14679
#103780 Alcohol dependence P08172
P14416
P31645
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#614373 Amyotrophic lateral sclerosis 16, juvenile; als16 Q99720
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#218030 Apparent mineralocorticoid excess; ame P80365
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#608584 Asthma-related traits, susceptibility to, 2 Q6W5P4
#208900 Ataxia-telangiectasia; at Q13315
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#601816 Bilirubin, serum level of, quantitative trait locus 1; biliqtl1 P22309
#210900 Bloom syndrome; blm P54132
#602025 Body mass index quantitative trait locus 9; bmiq9 P41968
#114480 Breast cancer P38398
#604370 Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 P38398
#300615 Brunner syndrome P21397
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#118300 Charcot-marie-tooth disease and deafness Q01453
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#118220 Charcot-marie-tooth disease, demyelinating, type 1a; cmt1a Q01453
#114500 Colorectal cancer; crc P84022
#613093 Cone dystrophy 4; cod4 P51160
#604931 Cortisone reductase deficiency 1; cortrd1 P28845
#218800 Crigler-najjar syndrome, type i P22309
P22310
#606785 Crigler-najjar syndrome, type ii P22309
P22310
#162800 Cyclic neutropenia P08246
#612522 Diabetes mellitus, insulin-dependent, 22; iddm22 P51681
#119900 Digital clubbing, isolated congenital P15428
#607208 Dravet syndrome P35498
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#237500 Dubin-johnson syndrome; djs Q92887
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#613721 Epileptic encephalopathy, early infantile, 11; eiee11 Q99250
#133239 Esophageal cancer P04637
#615363 Estrogen resistance; estrr P03372
#301500 Fabry disease P06280
#600274 Frontotemporal dementia; ftd P10636
#613659 Gastric cancer P04626
#137215 Gastric cancer, hereditary diffuse; hdgc P04626
#608013 Gaucher disease, perinatal lethal P04062
#230800 Gaucher disease, type i P04062
#230900 Gaucher disease, type ii P04062
#231000 Gaucher disease, type iii P04062
#231005 Gaucher disease, type iiic P04062
#604403 Generalized epilepsy with febrile seizures plus, type 2; gefsp2 P35498
#231095 Ghosal hematodiaphyseal dysplasia; ghdd P24557
#143500 Gilbert syndrome P22309
P22310
#137800 Glioma susceptibility 1; glm1 O75874
P04626
#232300 Glycogen storage disease ii P10253
#139393 Guillain-barre syndrome, familial; gbs Q01453
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610140 Heart-hand syndrome, slovenian type P02545
#609423 Human immunodeficiency virus type 1, susceptibility to P41597
P51681
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#237450 Hyperbilirubinemia, rotor type; hblrr Q9NPD5
Q9Y6L6
#237900 Hyperbilirubinemia, transient familial neonatal; hblrtfn P22309
#143860 Hyperchlorhidrosis, isolated O43570
#145000 Hyperparathyroidism 1; hrpt1 O00255
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#145900 Hypertrophic neuropathy of dejerine-sottas Q01453
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#612244 Inflammatory bowel disease 13; ibd13 P08183
#603932 Intervertebral disc disease; idd P14780
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#613688 Long qt syndrome 2; lqt2 Q12809
#211980 Lung cancer P00533
P04626
P04637
#608516 Major depressive disorder; mdd P08172
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#174800 Mccune-albright syndrome; mas P63092
#300705 Mental retardation, x-linked 17; mrx17 Q99714
%300852 Mental retardation, x-linked 88; mrx88 P50052
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#613073 Metaphyseal anadysplasia 2; mandp2 P14780
#609634 Migraine, familial hemiplegic, 3; fhm3 P35498
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#126200 Multiple sclerosis, susceptibility to; ms P08575
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#159900 Myoclonic dystonia P14416
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#162500 Neuropathy, hereditary, with liability to pressure palsies; hnpp Q01453
#202700 Neutropenia, severe congenital, 1, autosomal dominant; scn1 P08246
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#257220 Niemann-pick disease, type c1; npc1 O15118
#163500 Night blindness, congenital stationary, autosomal dominant 2; csnbad2 P35913
#601665 Obesity P32245
#164230 Obsessive-compulsive disorder; ocd P31645
#604715 Orthostatic intolerance P23975
#166350 Osseous heteroplasia, progressive; poh P63092
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#167000 Ovarian cancer P04626
P38398
#614320 Pancreatic cancer, susceptibility to, 4; pnca4 P38398
#260500 Papilloma of choroid plexus; cpp P04637
#168600 Parkinson disease, late-onset; pd P04062
#260540 Parkinson-dementia syndrome P10636
#613135 Parkinsonism-dystonia, infantile; pkdys Q01959
#172700 Pick disease of brain P10636
#610475 Pigmented nodular adrenocortical disease, primary, 2; ppnad2 Q9HCR9
#614190 Pigmented nodular adrenocortical disease, primary, 3; ppnad3 O95263
#102200 Pituitary adenoma, growth hormone-secreting P63092
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#607276 Resting heart rate, variation in P08588
#275210 Restrictive dermopathy, lethal P02545
#610024 Retinal cone dystrophy 3a; rcd3a Q13956
#613801 Retinitis pigmentosa 40; rp40 P35913
#613810 Retinitis pigmentosa 43; rp43 P16499
#613582 Retinitis pigmentosa 57; rp57 P18545
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#607745 Seizures, benign familial infantile, 3; bfis3 Q99250
#608971 Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-positive P08575
#609620 Short qt syndrome 1; sqt1 Q12809
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#253300 Spinal muscular atrophy, type i; sma1 Q16637
#253550 Spinal muscular atrophy, type ii; sma2 Q16637
#253400 Spinal muscular atrophy, type iii; sma3 Q16637
#271150 Spinal muscular atrophy, type iv; sma4 Q16637
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#609161 Striatal degeneration, autosomal dominant; adsd O95263
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#187950 Thrombocythemia 1; thcyt1 P40225
#188570 Thyroid hormone resistance, generalized, autosomal dominant; grth P10828
#274300 Thyroid hormone resistance, generalized, autosomal recessive; grth P10828
#145650 Thyroid hormone resistance, selective pituitary; prth P10828
#190300 Tremor, hereditary essential, 1; etm1 P35462
#610379 West nile virus, susceptibility to P51681
#278300 Xanthinuria, type i P47989
#112100 Yt blood group antigen P22303

KEGG DISEASE (121)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
P04637 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H00136 Niemann-Pick disease type C (NPC) O15118 (related)
H01302 Hyperchlorhidrosis isolated (HCHLH) O43570 (related)
H00021 Renal cell carcinoma O43570 (marker)
P04637 (marker)
Q16790 (marker)
H00260 Pigmented micronodular adrenocortical disease (PPNAD) O95263 (related)
Q9HCR9 (related)
H00016 Oral cancer P00533 (related)
P00533 (marker)
P04637 (related)
P04637 (marker)
H00017 Esophageal cancer P00533 (related)
P04637 (related)
P04637 (marker)
P35354 (related)
H00018 Gastric cancer P00533 (related)
P04626 (related)
P04637 (related)
H00022 Bladder cancer P00533 (related)
P04626 (related)
P04637 (related)
H00028 Choriocarcinoma P00533 (related)
P03956 (related)
P04626 (related)
P04637 (related)
H00030 Cervical cancer P00533 (related)
P04626 (related)
H00042 Glioma P00533 (related)
P00533 (marker)
P04637 (related)
P04637 (marker)
H00055 Laryngeal cancer P00533 (related)
P00533 (marker)
P04637 (related)
P04637 (marker)
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (related)
H00081 Hashimoto's thyroiditis P01215 (marker)
H00082 Graves' disease P01215 (marker)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P01215 (marker)
P16473 (related)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
Q01453 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
H00563 Emery-Dreifuss muscular dystrophy P02545 (related)
H00590 Congenital muscular dystrophies (CMD/MDC) P02545 (related)
H00593 Limb-girdle muscular dystrophy (LGMD) P02545 (related)
H00601 Hutchinson-Gilford progeria syndrome P02545 (related)
H00663 Restrictive dermopathy P02545 (related)
H00665 Mandibuloacral dysplasia P02545 (related)
H01216 Left ventricular noncompaction (LVNC) P02545 (related)
H00026 Endometrial Cancer P03372 (marker)
P04626 (related)
P04637 (related)
Q92731 (marker)
H00066 Lewy body dementia (LBD) P04062 (related)
H00126 Gaucher disease P04062 (related)
H00426 Defects in the degradation of ganglioside P04062 (related)
H00810 Progressive myoclonic epilepsy (PME) P04062 (related)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
P11511 (related)
H00019 Pancreatic cancer P04626 (related)
P04637 (related)
P04637 (marker)
H00027 Ovarian cancer P04626 (related)
P04637 (related)
P38398 (related)
H00031 Breast cancer P04626 (related)
P04626 (marker)
P04637 (related)
P38398 (related)
H00046 Cholangiocarcinoma P04626 (related)
P04637 (related)
P35354 (related)
H00004 Chronic myeloid leukemia (CML) P04637 (related)
H00005 Chronic lymphocytic leukemia (CLL) P04637 (related)
Q13315 (related)
H00006 Hairy-cell leukemia P04637 (related)
H00008 Burkitt lymphoma P04637 (related)
H00009 Adult T-cell leukemia P04637 (related)
H00010 Multiple myeloma P04637 (related)
H00013 Small cell lung cancer P04637 (related)
H00014 Non-small cell lung cancer P04637 (related)
H00015 Malignant pleural mesothelioma P04637 (related)
H00020 Colorectal cancer P04637 (related)
P04637 (marker)
H00025 Penile cancer P04637 (related)
P04637 (marker)
P14780 (related)
P35354 (related)
H00029 Vulvar cancer P04637 (related)
H00032 Thyroid cancer P04637 (related)
H00036 Osteosarcoma P04637 (related)
P08684 (marker)
H00038 Malignant melanoma P04637 (related)
P14679 (marker)
H00039 Basal cell carcinoma P04637 (related)
H00040 Squamous cell carcinoma P04637 (related)
H00041 Kaposi's sarcoma P04637 (related)
H00044 Cancer of the anal canal P04637 (related)
H00047 Gallbladder cancer P04637 (related)
H00048 Hepatocellular carcinoma P04637 (related)
H00881 Li-Fraumeni syndrome P04637 (related)
H01007 Choroid plexus papilloma P04637 (related)
H00093 Combined immunodeficiencies (CIDs) P06239 (related)
H00125 Fabry disease P06280 (related)
H00079 Asthma P07550 (related)
H00100 Neutropenic disorders P08246 (related)
H00091 T-B+Severe combined immunodeficiencies (SCIDs) P08575 (related)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00024 Prostate cancer P10275 (related)
H00062 Spinal and bulbar muscular atrophy (SBMA) P10275 (related)
H00608 46,XY disorders of sex development (Disorders in androgen synthesis or action) P10275 (related)
H00609 46,XY disorders of sex development (Other) P10275 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00794 Aromatase excess syndrome P11511 (related)
H01205 Coumarin resistance P11712 (related)
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00479 Metaphyseal dysplasias P14780 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H00527 Retinitis pigmentosa (RP) P16499 (related)
P18545 (related)
P35913 (related)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)
H00548 Brunner syndrome P21397 (related)
H00208 Hyperbilirubinemia P22309 (related)
Q92887 (related)
H01031 Orthostatic intolerance (OI) P23975 (related)
H00490 Diaphyseal dysplasia with anemia (Ghosal) P24557 (related)
H01111 Cortisone reductase deficiency (CRD) P28845 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00775 Familial or sporadic hemiplegic migraine P35498 (related)
H00783 Febrile seizures P35498 (related)
H00787 Congenital stationary night blindness (CSNB) P35913 (related)
H00227 Congenital amegakaryocytic thrombocytopenia (CAMT) P40225 (marker)
H00192 Xanthinuria P47989 (related)
H00480 Non-syndromic X-linked mental retardation P50052 (related)
Q99714 (related)
H00481 Cone-rod dystrophy and cone dystrophy P51160 (related)
Q13956 (related)
H00094 DNA repair defects P54132 (related)
Q13315 (related)
H00296 Defects in RecQ helicases P54132 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00259 Apparent mineralocorticoid excess syndrome P80365 (related)
H01296 Hereditary neuropathy with liability to pressure palsies (HNPP) Q01453 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00720 Long QT syndrome Q12809 (related)
H00725 Short QT syndrome Q12809 (related)
H00064 Ataxia telangiectasia (AT) Q13315 (related)
H00848 Ataxia with ocular apraxia (AOA) Q13315 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)
H00606 Early infantile epileptic encephalopathy Q99250 (related)
H00806 Benign familial neonatal and infantile epilepsies Q99250 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (related)
H00658 Syndromic X-linked mental retardation Q99714 (related)
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency Q99714 (related)

Diseases related to CTD interactions

81 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
C538231 Adenocarcinoma of lung C00002488
D003920 Diabetes Mellitus C00002488
D006943 Hyperglycemia C00002488
D009361 Neoplasm Invasiveness C00002488
D015746 Abdominal Pain C00031079
D000138 Acidosis C00031079
D000544 Alzheimer Disease C00031079
D000707 Anaphylaxis C00031079
D000787 Angina Pectoris C00031079
D000799 Angioedema C00031079
D001002 Anuria C00031079
D001049 Apnea C00031079
D001145 Arrhythmias, Cardiac C00031079
D001281 Atrial Fibrillation C00031079
D054537 Atrioventricular Block C00031079
D001919 Bradycardia C00031079
D001927 Brain Diseases C00031079
D002545 Brain Ischemia C00031079
D001986 Bronchial Spasm C00031079
D002311 Cardiomyopathy, Dilated C00031079
D002637 Chest Pain C00031079
D002779 Cholestasis C00031079
D003324 Coronary Artery Disease C00031079
D003327 Coronary Disease C00031079
D003329 Coronary Vasospasm C00031079
D003967 Diarrhea C00031079
D004108 Dilatation, Pathologic C00031079
D004244 Dizziness C00031079
D004408 Dysgeusia C00031079
D004409 Dyskinesia, Drug-Induced C00031079
D004417 Dyspnea C00031079
D005483 Flushing C00031079
D042882 Gallstones C00031079
D005767 Gastrointestinal Diseases C00031079
D005921 Glomerulonephritis C00031079
D006212 Hallucinations C00031079
D006261 Headache C00031079
D006323 Heart Arrest C00031079
D006327 Heart Block C00031079
D006331 Heart Diseases C00031079
D006333 Heart Failure C00031079
D006463 Hemolytic-Uremic Syndrome C00031079
D006470 Hemorrhage C00031079
D006940 Hyperemia C00031079
D006973 Hypertension C00031079
D006976 Hypertension, Pulmonary C00031079
D007022 Hypotension C00031079
D007174 Impulse Control Disorders C00031079
D007431 Intraoperative Complications C00031079
D007511 Ischemia C00031079
D002546 Ischemic Attack, Transient C00031079
D007964 Leukocytosis C00031079
D008881 Migraine Disorders C00031079
D008944 Mitral Valve Insufficiency C00031079
D009072 Moyamoya Disease C00031079
D009203 Myocardial Infarction C00031079
D017202 Myocardial Ischemia C00031079
D017682 Myocardial Stunning C00031079
D009325 Nausea C00031079
D009369 Neoplasms C00031079
D009401 Nephrosis C00031079
D010146 Pain C00031079
D010292 Paresthesia C00031079
D056627 Peritoneal Fibrosis C00031079
D020795 Photophobia C00031079
D011507 Proteinuria C00031079
D015427 Reperfusion Injury C00031079
D012770 Shock, Cardiogenic C00031079
D054138 Sinus Arrest, Cardiac C00031079
D020521 Stroke C00031079
D013345 Subarachnoid Hemorrhage C00031079
D013375 Substance Withdrawal Syndrome C00031079
D013575 Syncope C00031079
D017180 Tachycardia, Ventricular C00031079
D054549 Takotsubo Cardiomyopathy C00031079
D013927 Thrombosis C00031079
D020246 VENOUS THROMBOSIS C00031079
D018487 Ventricular Dysfunction, Left C00031079
D018879 Ventricular Premature Complexes C00031079
D014717 Vertigo C00031079
D014839 Vomiting C00031079