Species

KNApSAcK Entry

Organism name Zanthoxylum ailanthoides
Genus Zanthoxylum
Family Rutaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Zanthoxylum ailanthoides
Linked NCBI taxonomy ID 159071
Linked level species

Family

Family in NCBI taxonomy Rutaceae
ID 23513

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (27)

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
C00001861 External link 512 Glaucine
/ S-(+)-Glaucine
/ O,O-Dimethylisoboldine
CHEMBL36536
CHEMBL228082
14 / 8 / 6 No. 20 No. 4
C00003738 External link 512 beta-Amyrin
/ beta-Amirin
/ beta-Amyrine
/ beta-Amyrenol
C036380
0 / 4 No. 23 No. 51
C00002631 External link 512 (+)-Lirioresinol B
/ (+)-Syringaresinol
CHEMBL361362
CHEMBL402653
C042192
1 / 0 / 0 No. 38 No. 21
C00007190 External link 512 (+)-Pinoresinol
CHEMBL267963
CHEMBL487611
CHEMBL460862
C103298
7 / 5 / 6 No. 38 No. 21
C00007192 External link 512 (+)-Epipinoresinol
CHEMBL267963
CHEMBL487611
CHEMBL460862
7 / 5 / 6 No. 38 No. 21
C00024654 External link 512 Decarine
/ Rutaceline
CHEMBL458702
No. 254 No. 4
C00024655 External link 512 Norchelerythrine
/ O-Methyldecarine
/ N-Norchelerythrine
/ De-N-methylchelerythrine
/ Des-N-methylchelerythrine
CHEMBL1182694
No. 254 No. 4
C00000604 External link 512 (-)-Secoisolariciresinol
CHEMBL368347
C060283
2 / 1 / 1 1 / 0 No. 282 No. 21
C00002159 External link 512 gamma-Fagarine
/ 4,8-Dimethoxyfuro[2,3-b]quinoline
CHEMBL252925
C049193
8 / 14 / 7 No. 368 No. 7
C00026410 External link 512 Confusameline
/ 7-Hydroxydictamnine
/ 7-O-Demethylevolitrine
CHEMBL503574
No. 368 No. 7
C00047162 External link 512 Ailanthamide
CHEMBL556469
No. 499
C00007194 External link 512 (+)-Episesamin
CHEMBL43469
CHEMBL252915
CHEMBL1572261
CHEMBL1591714
CHEMBL1708854
CHEMBL1904496
CHEMBL1968861
20 / 24 / 15 No. 621 No. 21
C00002608 External link 512 Hinokinin
/ Hinoquinin
/ (-)-Hinokinin
/ (-)-Hinoquinin
CHEMBL180970
CHEMBL182073
CHEMBL242011
C475934
2 / 1 / 1 No. 629 No. 21
C00002505 External link 512 Xanthyletin
CHEMBL303846
C020814
29 / 43 / 58 No. 750 No. 25
C00007558 External link 512 Syringaldehyde
/ 4-Hydroxy-3,5-dimethoxybenzaldehyde
CHEMBL225303
C069665
No. 856
C00002498 External link 512 Scoparone
/ 6,7-Dimethoxycoumarin
/ Aesculetin dimethyl ether
CHEMBL325864
C018145
4 / 2 / 2 6 / 0 No. 864 No. 25
C00000575 External link 512 Bergaptan
CHEMBL24171
C022909
22 / 22 / 17 0 / 3 No. 1282 No. 25
C00026361 External link 512 Platydesmine
/ (+)-Platydesmine
No. 1467 No. 7
C00002657 External link 512 p-Formylphenol
/ 4-Hydroxybenzaldehyde
/ p-Hydroxybenzaldehyde
CHEMBL14193
C011483
3 / 2 / 2 No. 2076
C00030751 External link 512 Methyl 4-hydroxybenzoate
CHEMBL325372
C015358
102 / 49 / 57 3 / 0 No. 2169
C00033844 External link 512 Evofolin B
/ (-)-Evofolin B
CHEMBL448601
CHEMBL602133
No. 2211
C00026423 External link 512 Edulitine
/ Robustinin
/ Robustinine
CHEMBL256497
No. 2421 No. 7
C00026442 External link 512 Integriquinolone
No. 3424
C00047311 External link 512 N-(4-Methoxyphenethyl)-N-methylbenzamide
CHEMBL551703
No. 4049
C00047149 External link 512 4-(4'-Hydroxy-3'-methylbutoxy)benzaldehyde
No. 5180
C00047163 External link 512 Ailanthoidiol
No. 5180
C00047131 External link 512 (2E,4E)-N-Isobutyl-6-oxohepta-2,4-dienamide
CHEMBL556470
No. 6978

Human Protein / Gene in interactions

158 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00001861 C00002159 C00002505 C00007190 C00007192 C00007194 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000575 C00000604 C00002608 C00007194 C00030751 1 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000575 C00000604 C00002608 C00007194 C00030751 0 / 1
B2RXH2 Lysine-specific demethylase 4E Enzyme C00000575 C00001861 C00002159 C00002505 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00000575 C00002159 C00002505 C00007194 7 / 3
P00352 Retinal dehydrogenase 1 Enzyme C00000575 C00001861 C00002159 C00002505 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00000575 C00002505 C00007194 C00030751 0 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00007190 C00007192 C00030751 0 / 3
P56817 Beta-secretase 1 A1A C00000575 C00002498 C00002505 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00001861 C00002505 C00007194 4 / 3
Q9UNA4 DNA polymerase iota Enzyme C00001861 C00007194 C00030751 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00000575 C00002505 C00007194 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000575 C00007194 C00030751 1 / 1
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00000575 C00001861 C00002505 3 / 3
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000575 C00007194 C00030751 0 / 1
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002159 C00002505 C00007194 2 / 2
Q16790 Carbonic anhydrase 9 Lyase C00002505 C00030751 0 / 1
P22303 Acetylcholinesterase Hydrolase C00002505 C00030751 1 / 0
P43166 Carbonic anhydrase 7 Lyase C00002505 C00030751 0 / 0
P09917 Arachidonate 5-lipoxygenase Oxidoreductase C00007190 C00007192 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00007194 C00030751 0 / 0
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00007190 C00007192 0 / 0
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00007190 C00007192 5 / 3
Q07869 Peroxisome proliferator-activated receptor alpha NR1C1 C00007190 C00007192 0 / 0
Q16637 Survival motor neuron protein Unclassified protein C00002505 C00007194 4 / 1
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00002505 C00007194 0 / 0
P00915 Carbonic anhydrase 1 Lyase C00002505 C00030751 0 / 0
P38398 Breast cancer type 1 susceptibility protein Enzyme C00002159 C00002505 4 / 2
O75496 Geminin Unclassified protein C00001861 C00007194 0 / 0
P11509 Cytochrome P450 2A6 Cytochrome P450 2A6 C00000575 C00030751 0 / 0
O43570 Carbonic anhydrase 12 Lyase C00002505 C00030751 1 / 2
P04637 Cellular tumor antigen p53 Transcription Factor C00002505 C00030751 7 / 37
P00918 Carbonic anhydrase 2 Lyase C00002505 C00030751 1 / 2
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00001861 C00002159 1 / 0
Q9H0H5 Rac GTPase-activating protein 1 Unclassified protein C00007190 C00007192 0 / 0
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00002498 C00030751 1 / 1
P21917 D(4) dopamine receptor Dopamine receptor C00030751 0 / 0
P35367 Histamine H1 receptor Histamine receptor C00030751 0 / 0
Q01959 Sodium-dependent dopamine transporter Dopamine C00030751 1 / 0
P08912 Muscarinic acetylcholine receptor M5 Acetylcholine receptor C00030751 0 / 0
P18825 Alpha-2C adrenergic receptor Adrenergic receptor C00030751 0 / 0
P13945 Beta-3 adrenergic receptor Adrenergic receptor C00030751 0 / 0
P08183 Multidrug resistance protein 1 drug C00000575 1 / 0
P25024 C-X-C chemokine receptor type 1 CXC chemokine receptor C00030751 0 / 0
P06241 Tyrosine-protein kinase Fyn Src C00030751 0 / 0
Q08209 Serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform Ser_Thr C00030751 0 / 0
P07550 Beta-2 adrenergic receptor Adrenergic receptor C00030751 0 / 1
P05091 Aldehyde dehydrogenase, mitochondrial Oxidoreductase C00002498 1 / 1
Q9BQF6 Sentrin-specific protease 7 Enzyme C00001861 0 / 0
Q9GZR1 Sentrin-specific protease 6 Enzyme C00001861 0 / 0
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00030751 1 / 8
P11387 DNA topoisomerase 1 Isomerase C00002631 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00007194 2 / 3
P14416 D(2) dopamine receptor Dopamine receptor C00030751 2 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00030751 0 / 0
P37288 Vasopressin V1a receptor Vasopressin and oxytocin receptor C00030751 0 / 0
P41145 Kappa-type opioid receptor Opioid receptor C00030751 0 / 0
Q9Y271 Cysteinyl leukotriene receptor 1 Leukotriene receptor C00030751 0 / 0
P29274 Adenosine receptor A2a Adenosine receptor C00030751 0 / 0
P25929 Neuropeptide Y receptor type 1 Neuropeptide Y receptor C00030751 0 / 0
P16389 Potassium voltage-gated channel subfamily A member 2 KCNA, Kv1.x (Shaker) C00000575 0 / 0
P50052 Type-2 angiotensin II receptor Angiotensin receptor C00030751 1 / 1
Q14761 Protein tyrosine phosphatase receptor type C-associated protein Enzyme C00001861 0 / 0
O15296 Arachidonate 15-lipoxygenase B Enzyme C00007194 0 / 0
P17948 Vascular endothelial growth factor receptor 1 Vegfr C00030751 0 / 0
P41968 Melanocortin receptor 3 Melanocortin receptor C00030751 1 / 0
Q9ULX7 Carbonic anhydrase 14 Lyase C00030751 0 / 0
P42574 Caspase-3 C14 C00001861 0 / 0
P17405 Sphingomyelin phosphodiesterase Enzyme C00002505 2 / 2
P51649 Succinate-semialdehyde dehydrogenase, mitochondrial Oxidoreductase C00002657 1 / 1
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00030751 1 / 1
P14902 Indoleamine 2,3-dioxygenase 1 Enzyme C00002657 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00007194 2 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00000575 3 / 2
P51151 Ras-related protein Rab-9A Unclassified protein C00002505 0 / 0
O60656 UDP-glucuronosyltransferase 1-9 Enzyme C00030751 0 / 0
P37840 Alpha-synuclein Unclassified protein C00002505 4 / 2
P04035 3-hydroxy-3-methylglutaryl-coenzyme A reductase Oxidoreductase C00030751 0 / 0
P08913 Alpha-2A adrenergic receptor Adrenergic receptor C00030751 0 / 0
P25021 Histamine H2 receptor Histamine receptor C00030751 0 / 0
P30988 Calcitonin receptor Calcitonin receptor C00030751 0 / 0
P35462 D(3) dopamine receptor Dopamine receptor C00030751 1 / 0
P41143 Delta-type opioid receptor Opioid receptor C00030751 0 / 0
Q92731 Estrogen receptor beta NR3A2 C00030751 0 / 1
P41595 5-hydroxytryptamine receptor 2B Serotonin receptor C00030751 0 / 0
P25101 Endothelin-1 receptor Endothelin receptor C00030751 0 / 0
P30411 B2 bradykinin receptor Bradykinin receptor C00030751 0 / 0
P32245 Melanocortin receptor 4 Melanocortin receptor C00030751 1 / 0
Q96LD8 Sentrin-specific protease 8 Enzyme C00001861 0 / 0
P32238 Cholecystokinin receptor type A Cholecystokinin receptor C00030751 0 / 0
P08311 Cathepsin G S1A C00030751 0 / 0
Q99720 Sigma non-opioid intracellular receptor 1 Membrane receptor C00030751 1 / 0
P17658 Potassium voltage-gated channel subfamily A member 6 K C00000575 0 / 0
P03956 Interstitial collagenase M10A C00030751 0 / 1
P32241 Vasoactive intestinal polypeptide receptor 1 Vasoactive intestinal peptide receptor C00030751 0 / 0
P20813 Cytochrome P450 2B6 Cytochrome P450 2B6 C00000575 1 / 0
Q8N1Q1 Carbonic anhydrase 13 Lyase C00002505 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00007194 0 / 0
P04150 Glucocorticoid receptor NR3C1 C00030751 0 / 1
P08172 Muscarinic acetylcholine receptor M2 Acetylcholine receptor C00030751 2 / 0
P11229 Muscarinic acetylcholine receptor M1 Acetylcholine receptor C00030751 0 / 0
P21554 Cannabinoid receptor 1 Cannabinoid receptor C00030751 0 / 0
P31645 Sodium-dependent serotonin transporter Serotonin C00030751 2 / 0
P14780 Matrix metalloproteinase-9 M10A C00030751 2 / 2
P80404 4-aminobutyrate aminotransferase, mitochondrial Transferase C00002657 1 / 1
P04626 Receptor tyrosine-protein kinase erbB-2 TK tyrosine-protein kinase EGFR subfamily C00030751 5 / 9
P20309 Muscarinic acetylcholine receptor M3 Acetylcholine receptor C00030751 1 / 0
P21452 Substance-K receptor Neurokinin receptor C00030751 0 / 0
P51679 C-C chemokine receptor type 4 CC chemokine receptor C00030751 0 / 0
P51681 C-C chemokine receptor type 5 CC chemokine receptor C00030751 3 / 0
P50406 5-hydroxytryptamine receptor 6 Serotonin receptor C00030751 0 / 0
P41597 C-C chemokine receptor type 2 CC chemokine receptor C00030751 1 / 0
P04406 Glyceraldehyde-3-phosphate dehydrogenase Enzyme C00002505 0 / 0
P08575 Receptor-type tyrosine-protein phosphatase C Enzyme C00030751 2 / 1
P27361 Mitogen-activated protein kinase 3 Erk C00030751 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00030751 0 / 0
P17252 Protein kinase C alpha type Alpha C00030751 0 / 0
P29466 Caspase-1 C14 C00030751 0 / 0
P22001 Potassium voltage-gated channel subfamily A member 3 KCNA, Kv1.x (Shaker) C00000575 0 / 0
O15118 Niemann-Pick C1 protein Unclassified protein C00002505 1 / 1
P49146 Neuropeptide Y receptor type 2 Neuropeptide Y receptor C00030751 0 / 0
O76074 cGMP-specific 3',5'-cyclic phosphodiesterase PDE_5A C00030751 0 / 0
P03372 Estrogen receptor NR3A1 C00030751 1 / 1
P08588 Beta-1 adrenergic receptor Adrenergic receptor C00030751 1 / 0
P06746 DNA polymerase beta Enzyme C00002505 0 / 0
P28223 5-hydroxytryptamine receptor 2A Serotonin receptor C00030751 0 / 0
P28335 5-hydroxytryptamine receptor 2C Serotonin receptor C00030751 0 / 0
P35372 Mu-type opioid receptor Opioid receptor C00030751 0 / 0
P08173 Muscarinic acetylcholine receptor M4 Acetylcholine receptor C00030751 0 / 0
P25103 Substance-P receptor Neurokinin receptor C00030751 0 / 0
P25105 Platelet-activating factor receptor PAF receptor C00030751 0 / 0
P33032 Melanocortin receptor 5 Melanocortin receptor C00030751 0 / 0
Q16539 Mitogen-activated protein kinase 14 p38 C00030751 0 / 0
P33765 Adenosine receptor A3 Adenosine receptor C00030751 0 / 0
P05181 Cytochrome P450 2E1 Cytochrome P450 2E1 C00030751 0 / 0
P08246 Neutrophil elastase S1A C00030751 2 / 1
P22309 UDP-glucuronosyltransferase 1-1 Enzyme C00030751 5 / 1
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00030751 2 / 2
P19224 UDP-glucuronosyltransferase 1-6 Enzyme C00030751 0 / 0
P21728 D(1A) dopamine receptor Dopamine receptor C00030751 0 / 0
P10275 Androgen receptor NR3C4 C00000575 3 / 4
P23975 Sodium-dependent noradrenaline transporter Norepinephrine C00030751 1 / 1
P25100 Alpha-1D adrenergic receptor Adrenergic receptor C00030751 0 / 0
P30542 Adenosine receptor A1 Adenosine receptor C00030751 0 / 0
Q99700 Ataxin-2 Unclassified protein C00002505 1 / 1
P18089 Alpha-2B adrenergic receptor Adrenergic receptor C00030751 0 / 0
P24557 Thromboxane-A synthase Cytochrome P450 5A1 C00030751 1 / 1
P06239 Tyrosine-protein kinase Lck Src C00030751 0 / 1
P22460 Potassium voltage-gated channel subfamily A member 5 KCNA, Kv1.x (Shaker) C00000575 1 / 1
P25025 C-X-C chemokine receptor type 2 CXC chemokine receptor C00030751 0 / 0
P48547 Potassium voltage-gated channel subfamily C member 1 K C00000575 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00002159 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00002505 1 / 0
P27338 Amine oxidase [flavin-containing] B Oxidoreductase C00002498 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00030751 0 / 0
Q09470 Potassium voltage-gated channel subfamily A member 1 KCNA, Kv1.x (Shaker) C00000575 1 / 1
P43351 DNA repair protein RAD52 homolog Unclassified protein C00001861 0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00007194 1 / 1

10 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
2099 ESR1, ER, ESR, ESRA, ESTRR, Era, NR3A1 estrogen receptor 1 C00030751
3952 LEP, LEPD, OB, OBS leptin C00030751
7031 TFF1, BCEI, D21S21, HP1.A, HPS2, pNR-2, pS2 trefoil factor 1 C00030751
6347 CCL2, GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1, SCYA2, SMC-CF chemokine (C-C motif) ligand 2 C00002498
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00002498
4790 NFKB1, EBP-1, KBF1, NF-kB1, NF-kappa-B, NF-kappaB, NFKB-p105, NFKB-p50, NFkappaB, p105, p50 nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 C00002498
4792 NFKBIA, IKBA, MAD-3, NFKBI nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha C00002498
5966 REL, C-Rel v-rel avian reticuloendotheliosis viral oncogene homolog C00002498
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00002498
8856 NR1I2, BXR, ONR1, PAR, PAR1, PAR2, PARq, PRR, PXR, SAR, SXR nuclear receptor subfamily 1, group I, member 2 C00000604

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (102)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#100100 Abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism P20309
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#103780 Alcohol dependence P08172
P14416
P31645
#610251 Alcohol sensitivity, acute P05091
#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
#612240 Atrial fibrillation, familial, 7; atfb7 P22460
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#601816 Bilirubin, serum level of, quantitative trait locus 1; biliqtl1 P22309
#602025 Body mass index quantitative trait locus 9; bmiq9 P41968
%606641 Body mass index; bmi P37231
#114480 Breast cancer P38398
#604370 Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 P38398
#300615 Brunner syndrome P21397
#609338 Carotid intimal medial thickness 1 P37231
#114500 Colorectal cancer; crc P84022
#218800 Crigler-najjar syndrome, type i P22309
#606785 Crigler-najjar syndrome, type ii P22309
#162800 Cyclic neutropenia P08246
#127750 Dementia, lewy body; dlb P37840
#612522 Diabetes mellitus, insulin-dependent, 22; iddm22 P51681
#119900 Digital clubbing, isolated congenital P15428
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#614546 Efavirenz, poor metabolism of P20813
#160120 Episodic ataxia, type 1; ea1 Q09470
#133239 Esophageal cancer P04637
#615363 Estrogen resistance; estrr P03372
#600274 Frontotemporal dementia; ftd P10636
#613163 Gaba-transaminase deficiency P80404
#613659 Gastric cancer P04626
#137215 Gastric cancer, hereditary diffuse; hdgc P04626
#231095 Ghosal hematodiaphyseal dysplasia; ghdd P24557
#143500 Gilbert syndrome P22309
#137800 Glioma susceptibility 1; glm1 O75874
P04626
P37231
#609423 Human immunodeficiency virus type 1, susceptibility to P41597
P51681
#237900 Hyperbilirubinemia, transient familial neonatal; hblrtfn P22309
#143860 Hyperchlorhidrosis, isolated O43570
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#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
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#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
#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
#126200 Multiple sclerosis, susceptibility to; ms P08575
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#159900 Myoclonic dystonia P14416
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#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
#601665 Obesity P32245
P37231
#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
#168601 Parkinson disease 1, autosomal dominant; park1 P37840
#605543 Parkinson disease 4, autosomal dominant; park4 P37840
#168600 Parkinson disease, late-onset; pd P37840
#260540 Parkinson-dementia syndrome P10636
#613135 Parkinsonism-dystonia, infantile; pkdys Q01959
#172700 Pick disease of brain P10636
#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
#608971 Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-positive P08575
#609620 Short qt syndrome 1; sqt1 Q12809
#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
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#271980 Succinic semialdehyde dehydrogenase deficiency; ssadhd P51649
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#190300 Tremor, hereditary essential, 1; etm1 P35462
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#610379 West nile virus, susceptibility to P51681
#278300 Xanthinuria, type i P47989
#112100 Yt blood group antigen P22303

KEGG DISEASE (90)

KEGG name UniProt
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)
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)
H00026 Endometrial Cancer P03372 (marker)
P04626 (related)
P04637 (related)
Q92731 (marker)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (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)
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)
P37231 (related)
H00033 Adrenal carcinoma P04637 (related)
H00036 Osteosarcoma P04637 (related)
P08684 (marker)
H00038 Malignant melanoma P04637 (related)
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)
H01071 Acute alcohol sensitivity P05091 (related)
H00093 Combined immunodeficiencies (CIDs) P06239 (related)
H00079 Asthma P07550 (related)
H00100 Neutropenic disorders P08246 (related)
H00091 T-B+Severe combined immunodeficiencies (SCIDs) P08575 (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)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H01205 Coumarin resistance P11712 (related)
H00479 Metaphyseal dysplasias P14780 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (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)
H00731 Atrial fibrillation P22460 (related)
H01031 Orthostatic intolerance (OI) P23975 (related)
H00490 Diaphyseal dysplasia with anemia (Ghosal) P24557 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00420 Familial partial lipodystrophy (FPL) P37231 (related)
H00057 Parkinson's disease (PD) P37840 (related)
H00066 Lewy body dementia (LBD) P37840 (related)
H00192 Xanthinuria P47989 (related)
H00480 Non-syndromic X-linked mental retardation P50052 (related)
Q99714 (related)
H00835 Succinic semialdehyde dehydrogenase (SSADH) deficiency P51649 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H01257 GABA-transaminase deficiency P80404 (related)
H00749 Episodic ataxias Q09470 (related)
H00720 Long QT syndrome Q12809 (related)
H00725 Short QT syndrome Q12809 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (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

7 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D006505 Hepatitis C00000575
D010787 Photosensitivity Disorders C00000575
D011565 Psoriasis C00000575
D005157 Facial Pain C00003738
D006930 Hyperalgesia C00003738
D007249 Inflammation C00003738
D010146 Pain C00003738