Species

KNApSAcK Entry

Organism name Baptisia spp.
Genus Baptisia
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Baptisia
Linked NCBI taxonomy ID 49796
Linked level genus

Family

Family in NCBI taxonomy Fabaceae
ID 3803

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (13)

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
C00010107 External link 512 Sphaerobioside
/ Hirsutissimiside B
No. 1 No. 15
C00002553 External link 512 Ononin
/ Formononetin 7-O-glucoside
CHEMBL465980
11 / 14 / 40 No. 2 No. 15
C00010087 External link 512 Calycosin 7-O-glucoside
No. 2 No. 15
C00010119 External link 512 Oroboside
/ Orobol 7-O-glucoside
No. 2 No. 15
C00005373 External link 512 Hirsutrin
/ Isoquercetin
/ Isoquercetrin
/ (-)-Isoquercetrin
/ Quercetin 3-glucoside
/ Quercetin 3-O-beta-D-glucoside
/ Quercetin-3-O-beta-D-glucopyranoside
/ Quercetin 3-O-beta-D-glucopyranoside
/ (-)-Quercetin-3-O-beta-D-glucopyranoside
CHEMBL33027
CHEMBL309323
CHEMBL250450
CHEMBL251254
CHEMBL457304
CHEMBL1098724
CHEMBL2337335
CHEMBL2337336
38 / 43 / 34 No. 2 No. 15
C00002576 External link 512 Shekanin
/ Shekkanin
/ Tectoridin
/ Tectorigenin 7-O-glucoside
CHEMBL520214
C120040
0 / 2 No. 2 No. 15
C00005138 External link 512 Astragalin
/ Kaempferol 3-glucoside
/ Kaempferol 3-O-beta-D-glucoside
/ Kaempferol 3-O-beta-D-glucopyranoside
CHEMBL233930
CHEMBL453290
CHEMBL1572115
C001579
10 / 6 / 7 0 / 1 No. 2 No. 15
C00009389 External link 512 Cyclosin
/ Calycosin
/ 3'-Hydroxyformononetin
CHEMBL241608
10 / 9 / 6 No. 3 No. 15
C00002577 External link 512 Tectorigenin
/ 5,7,4'-Trihydroxy-6-methoxyisoflavone
CHEMBL242740
C120039
1 / 1 / 8 No. 3 No. 15
C00002509 External link 512 Betavulgarin
/ 2'-Hydroxy-5-methoxy-6,7-methylenedioxyisoflavone
No. 27 No. 15
C00002554 External link 512 Orobol
/ Santol
/ Norsantal
/ 5,7,3',4'-Tetrahydroxyisoflavone
CHEMBL241609
C059811
1 / 1 / 8 No. 71 No. 15
C00002218 External link 512 Cytisine
/ (-)-Cytisine
CHEMBL47039
CHEMBL497939
CHEMBL1628606
C004712
27 / 36 / 33 6 / 1 No. 376 No. 3
C00002236 External link 512 Spartein
/ (-)-Spartein
CHEMBL412873
CHEMBL44625
CHEMBL172633
CHEMBL1328708
CHEMBL1492771
CHEMBL1740920
CHEMBL1908847
CHEMBL2010478
D013034
93 / 50 / 48 1 / 2 No. 424 No. 3

Human Protein / Gene in interactions

147 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q9UNA4 DNA polymerase iota Enzyme C00002553 C00005138 C00005373 C00009389 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00002553 C00005138 C00009389 0 / 0
P15121 Aldose reductase Enzyme C00002553 C00005138 C00005373 0 / 0
P02545 Prelamin-A/C Unclassified protein C00002218 C00002236 C00005373 11 / 10
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00002236 C00002554 C00002577 1 / 8
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00005138 C00005373 C00009389 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002218 C00005373 C00009389 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00002218 C00005373 C00009389 4 / 3
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00002218 C00002236 1 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00002236 C00005373 0 / 3
O00255 Menin Unclassified protein C00002218 C00002236 2 / 5
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00002218 C00005373 0 / 0
P06746 DNA polymerase beta Enzyme C00005373 C00009389 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002218 C00002236 0 / 1
P04062 Glucosylceramidase Enzyme C00002218 C00005373 6 / 4
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00002218 C00002236 1 / 1
P35372 Mu-type opioid receptor Opioid receptor C00002236 C00005373 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00005373 C00009389 0 / 0
O15118 Niemann-Pick C1 protein Unclassified protein C00002553 C00009389 1 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00002218 C00002236 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00002236 C00005373 0 / 0
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002218 C00002236 1 / 2
P14679 Tyrosinase Oxidoreductase C00005138 C00005373 4 / 2
Q9Y253 DNA polymerase eta Enzyme C00005138 C00005373 1 / 1
Q13951 Core-binding factor subunit beta Unclassified protein C00002218 C00005373 0 / 1
P41143 Delta-type opioid receptor Opioid receptor C00002236 C00005373 0 / 0
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00002236 C00002553 1 / 1
P38398 Breast cancer type 1 susceptibility protein Enzyme C00002553 C00009389 4 / 2
P51151 Ras-related protein Rab-9A Unclassified protein C00002553 C00009389 0 / 0
O75496 Geminin Unclassified protein C00002218 C00005373 0 / 0
P41145 Kappa-type opioid receptor Opioid receptor C00002236 C00005373 0 / 0
P18825 Alpha-2C adrenergic receptor Adrenergic receptor C00002236 C00005373 0 / 0
Q01196 Runt-related transcription factor 1 Unclassified protein C00002218 C00005373 1 / 4
P07237 Protein disulfide-isomerase Enzyme C00005138 C00005373 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00002218 C00002236 0 / 1
Q08209 Serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform Ser_Thr C00002236 0 / 0
P06241 Tyrosine-protein kinase Fyn Src C00002236 0 / 0
P30926 Neuronal acetylcholine receptor subunit beta-4 CHRN beta C00002218 0 / 0
P32297 Neuronal acetylcholine receptor subunit alpha-3 CHRN alpha C00002218 1 / 0
Q07001 Acetylcholine receptor subunit delta CHRN delta C00002218 3 / 2
P43681 Neuronal acetylcholine receptor subunit alpha-4 CHRN alpha C00002218 1 / 1
P07510 Acetylcholine receptor subunit gamma CHRN gamma C00002218 2 / 1
P17787 Neuronal acetylcholine receptor subunit beta-2 CHRN beta C00002218 1 / 1
P02708 Acetylcholine receptor subunit alpha CHRN alpha C00002218 3 / 2
P11230 Acetylcholine receptor subunit beta CHRN beta C00002218 2 / 1
P25024 C-X-C chemokine receptor type 1 CXC chemokine receptor C00002236 0 / 0
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00005373 1 / 0
P13945 Beta-3 adrenergic receptor Adrenergic receptor C00002236 0 / 0
P14416 D(2) dopamine receptor Dopamine receptor C00002236 2 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00002236 0 / 0
P37288 Vasopressin V1a receptor Vasopressin and oxytocin receptor C00002236 0 / 0
P08912 Muscarinic acetylcholine receptor M5 Acetylcholine receptor C00002236 0 / 0
Q9Y271 Cysteinyl leukotriene receptor 1 Leukotriene receptor C00002236 0 / 0
P29274 Adenosine receptor A2a Adenosine receptor C00002236 0 / 0
P25929 Neuropeptide Y receptor type 1 Neuropeptide Y receptor C00002236 0 / 0
P50052 Type-2 angiotensin II receptor Angiotensin receptor C00002236 1 / 1
P17948 Vascular endothelial growth factor receptor 1 Vegfr C00002236 0 / 0
P41968 Melanocortin receptor 3 Melanocortin receptor C00002236 1 / 0
P36888 Receptor-type tyrosine-protein kinase FLT3 Pdgfr C00005373 1 / 1
P11509 Cytochrome P450 2A6 Cytochrome P450 2A6 C00002236 0 / 0
P39748 Flap endonuclease 1 Enzyme C00005373 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00002236 0 / 0
Q01959 Sodium-dependent dopamine transporter Dopamine C00002236 1 / 0
P35367 Histamine H1 receptor Histamine receptor C00002236 0 / 0
P25021 Histamine H2 receptor Histamine receptor C00002236 0 / 0
P04035 3-hydroxy-3-methylglutaryl-coenzyme A reductase Oxidoreductase C00002236 0 / 0
P08913 Alpha-2A adrenergic receptor Adrenergic receptor C00002236 0 / 0
P21917 D(4) dopamine receptor Dopamine receptor C00002236 0 / 0
P30988 Calcitonin receptor Calcitonin receptor C00002236 0 / 0
P35462 D(3) dopamine receptor Dopamine receptor C00002236 1 / 0
P07550 Beta-2 adrenergic receptor Adrenergic receptor C00002236 0 / 1
Q92731 Estrogen receptor beta NR3A2 C00002236 0 / 1
P41595 5-hydroxytryptamine receptor 2B Serotonin receptor C00002236 0 / 0
P05091 Aldehyde dehydrogenase, mitochondrial Oxidoreductase C00002553 1 / 1
P25101 Endothelin-1 receptor Endothelin receptor C00002236 0 / 0
P30411 B2 bradykinin receptor Bradykinin receptor C00002236 0 / 0
P32245 Melanocortin receptor 4 Melanocortin receptor C00002236 1 / 0
P32238 Cholecystokinin receptor type A Cholecystokinin receptor C00002236 0 / 0
P08311 Cathepsin G S1A C00002236 0 / 0
Q99720 Sigma non-opioid intracellular receptor 1 Membrane receptor C00002236 1 / 0
P03956 Interstitial collagenase M10A C00002236 0 / 1
P32241 Vasoactive intestinal polypeptide receptor 1 Vasoactive intestinal peptide receptor C00002236 0 / 0
P00918 Carbonic anhydrase 2 Lyase C00002236 1 / 2
P09923 Intestinal-type alkaline phosphatase Enzyme C00005373 0 / 0
P05186 Alkaline phosphatase, tissue-nonspecific isozyme Enzyme C00005373 3 / 1
P83916 Chromobox protein homolog 1 Unclassified protein C00002218 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00002218 0 / 0
P04150 Glucocorticoid receptor NR3C1 C00002236 0 / 1
P08172 Muscarinic acetylcholine receptor M2 Acetylcholine receptor C00002236 2 / 0
P11229 Muscarinic acetylcholine receptor M1 Acetylcholine receptor C00002236 0 / 0
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00005373 1 / 1
P21554 Cannabinoid receptor 1 Cannabinoid receptor C00002236 0 / 0
P31645 Sodium-dependent serotonin transporter Serotonin C00002236 2 / 0
P04626 Receptor tyrosine-protein kinase erbB-2 TK tyrosine-protein kinase EGFR subfamily C00002236 5 / 9
P20309 Muscarinic acetylcholine receptor M3 Acetylcholine receptor C00002236 1 / 0
P21452 Substance-K receptor Neurokinin receptor C00002236 0 / 0
P51679 C-C chemokine receptor type 4 CC chemokine receptor C00002236 0 / 0
P51681 C-C chemokine receptor type 5 CC chemokine receptor C00002236 3 / 0
P50406 5-hydroxytryptamine receptor 6 Serotonin receptor C00002236 0 / 0
P36544 Neuronal acetylcholine receptor subunit alpha-7 CHRN alpha C00002218 0 / 0
P06280 Alpha-galactosidase A Enzyme C00005373 1 / 1
P41597 C-C chemokine receptor type 2 CC chemokine receptor C00002236 1 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00005138 0 / 0
P10696 Alkaline phosphatase, placental-like Enzyme C00005373 0 / 1
P08575 Receptor-type tyrosine-protein phosphatase C Enzyme C00002236 2 / 1
P14780 Matrix metalloproteinase-9 M10A C00002236 2 / 2
Q9UNQ0 ATP-binding cassette sub-family G member 2 ATP binding cassette C00005373 2 / 0
P27361 Mitogen-activated protein kinase 3 Erk C00002236 0 / 0
P17252 Protein kinase C alpha type Alpha C00002236 0 / 0
O76074 cGMP-specific 3',5'-cyclic phosphodiesterase PDE_5A C00002236 0 / 0
P03372 Estrogen receptor NR3A1 C00002236 1 / 1
P08588 Beta-1 adrenergic receptor Adrenergic receptor C00002236 1 / 0
P22303 Acetylcholinesterase Hydrolase C00002236 1 / 0
P28223 5-hydroxytryptamine receptor 2A Serotonin receptor C00002236 0 / 0
P28335 5-hydroxytryptamine receptor 2C Serotonin receptor C00002236 0 / 0
P29466 Caspase-1 C14 C00002236 0 / 0
P08173 Muscarinic acetylcholine receptor M4 Acetylcholine receptor C00002236 0 / 0
P25103 Substance-P receptor Neurokinin receptor C00002236 0 / 0
P25105 Platelet-activating factor receptor PAF receptor C00002236 0 / 0
P33032 Melanocortin receptor 5 Melanocortin receptor C00002236 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00005373 1 / 1
P49146 Neuropeptide Y receptor type 2 Neuropeptide Y receptor C00002236 0 / 0
P05181 Cytochrome P450 2E1 Cytochrome P450 2E1 C00002236 0 / 0
Q16539 Mitogen-activated protein kinase 14 p38 C00002236 0 / 0
P33765 Adenosine receptor A3 Adenosine receptor C00002236 0 / 0
P08246 Neutrophil elastase S1A C00002236 2 / 1
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00002553 0 / 0
P08908 5-hydroxytryptamine receptor 1A Serotonin receptor C00005373 1 / 0
P23975 Sodium-dependent noradrenaline transporter Norepinephrine C00002236 1 / 1
P25100 Alpha-1D adrenergic receptor Adrenergic receptor C00002236 0 / 0
P30542 Adenosine receptor A1 Adenosine receptor C00002236 0 / 0
P18089 Alpha-2B adrenergic receptor Adrenergic receptor C00002236 0 / 0
P24557 Thromboxane-A synthase Cytochrome P450 5A1 C00002236 1 / 1
P06239 Tyrosine-protein kinase Lck Src C00002236 0 / 1
P25025 C-X-C chemokine receptor type 2 CXC chemokine receptor C00002236 0 / 0
P34949 Mannose-6-phosphate isomerase Enzyme C00005373 1 / 1
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00002236 2 / 2
P21728 D(1A) dopamine receptor Dopamine receptor C00002236 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00005373 0 / 0
Q99700 Ataxin-2 Unclassified protein C00005138 1 / 1
Q16637 Survival motor neuron protein Unclassified protein C00005373 4 / 1
Q9NPH5 NADPH oxidase 4 Enzyme C00005373 0 / 0
P04637 Cellular tumor antigen p53 Transcription Factor C00002553 7 / 37
Q15822 Neuronal acetylcholine receptor subunit alpha-2 CHRN alpha C00002218 1 / 1
P27338 Amine oxidase [flavin-containing] B Oxidoreductase C00002553 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00005373 0 / 0
P01215 Glycoprotein hormones alpha chain Unclassified protein C00005138 0 / 3

7 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
1135 CHRNA2 cholinergic receptor, nicotinic, alpha 2 (neuronal) C00002218
1136 CHRNA3, LNCR2, NACHRA3, PAOD2 cholinergic receptor, nicotinic, alpha 3 (neuronal) C00002218
1137 CHRNA4, BFNC, EBN, EBN1, NACHR, NACHRA4, NACRA4 cholinergic receptor, nicotinic, alpha 4 (neuronal) C00002218
1139 CHRNA7, CHRNA7-2, NACHRA7 cholinergic receptor, nicotinic, alpha 7 (neuronal) C00002218
1141 CHRNB2, EFNL3, nAChRB2 cholinergic receptor, nicotinic, beta 2 (neuronal) C00002218
1143 CHRNB4 cholinergic receptor, nicotinic, beta 4 (neuronal) C00002218
1565 CYP2D6, CPD6, CYP2D, CYP2D7AP, CYP2D7BP, CYP2D7P2, CYP2D8P2, CYP2DL1, CYPIID6, P450-DB1, P450C2D, P450DB1 cytochrome P450, family 2, subfamily D, polypeptide 6 (EC:1.14.14.1) C00002236

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (103)

OMIM preferred title UniProt
#100100 Abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism P20309
#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
#610251 Alcohol sensitivity, acute P05091
#614373 Amyotrophic lateral sclerosis 16, juvenile; als16 Q99720
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#614490 Blood group, junior system; jr Q9UNQ0
#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
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#602579 Congenital disorder of glycosylation, type ib; cdg1b P34949
#162800 Cyclic neutropenia P08246
#612522 Diabetes mellitus, insulin-dependent, 22; iddm22 P51681
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#600513 Epilepsy, nocturnal frontal lobe, 1; enfl1 P43681
#605375 Epilepsy, nocturnal frontal lobe, 3; enfl3 P17787
#610353 Epilepsy, nocturnal frontal lobe, 4; enfl4 Q15822
#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
#231095 Ghosal hematodiaphyseal dysplasia; ghdd P24557
#137800 Glioma susceptibility 1; glm1 P04626
#232300 Glycogen storage disease ii P10253
#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
#145000 Hyperparathyroidism 1; hrpt1 O00255
#146300 Hypophosphatasia, adult P05186
#241510 Hypophosphatasia, childhood P05186
#241500 Hypophosphatasia, infantile P05186
#603932 Intervertebral disc disease; idd P14780
#601626 Leukemia, acute myeloid; aml P36888
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#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
%300852 Mental retardation, x-linked 88; mrx88 P50052
#613073 Metaphyseal anadysplasia 2; mandp2 P14780
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#265000 Multiple pterygium syndrome, escobar variant; evmps P07510
#253290 Multiple pterygium syndrome, lethal type; lmps P02708
P07510
Q07001
#126200 Multiple sclerosis, susceptibility to; ms P08575
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#608931 Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency P11230
#608930 Myasthenic syndrome, congenital, fast-channel P02708
Q07001
#601462 Myasthenic syndrome, congenital, slow-channel; sccms P02708
P11230
Q07001
#159900 Myoclonic dystonia P14416
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#202700 Neutropenia, severe congenital, 1, autosomal dominant; scn1 P08246
#257220 Niemann-pick disease, type c1; npc1 O15118
#601665 Obesity P32245
#164230 Obsessive-compulsive disorder; ocd P31645
#604715 Orthostatic intolerance P23975
#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
#614674 Periodic fever, menstrual cycle-dependent P08908
#172700 Pick disease of brain P10636
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#607276 Resting heart rate, variation in P08588
#275210 Restrictive dermopathy, lethal P02545
#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
#612052 Smoking as a quantitative trait locus 3; sqtl3 P32297
#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
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#190300 Tremor, hereditary essential, 1; etm1 P35462
#138900 Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 Q9UNQ0
#610379 West nile virus, susceptibility to P51681
#278300 Xanthinuria, type i P47989
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253
#112100 Yt blood group antigen P22303

KEGG DISEASE (97)

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)
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)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (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)
H00770 Congenital myasthenic syndrome P02708 (related)
P11230 (related)
Q07001 (related)
H00986 Multiple pterygium syndrome P02708 (related)
P07510 (related)
Q07001 (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)
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)
Q01196 (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)
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)
H00021 Renal cell carcinoma P04637 (marker)
H01071 Acute alcohol sensitivity P05091 (related)
H00213 Hypophosphatasia P05186 (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)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00023 Testicular cancer P10696 (marker)
H01205 Coumarin resistance P11712 (related)
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00479 Metaphyseal dysplasias P14780 (related)
H00807 Autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) P17787 (related)
P43681 (related)
Q15822 (related)
H00548 Brunner syndrome P21397 (related)
H01031 Orthostatic intolerance (OI) P23975 (related)
H00490 Diaphyseal dysplasia with anemia (Ghosal) P24557 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00118 Congenital disorders of glycosylation (CDG) type I P34949 (related)
H00003 Acute myeloid leukemia (AML) P36888 (related)
Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00192 Xanthinuria P47989 (related)
H00480 Non-syndromic X-linked mental retardation P50052 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
Q03164 (related)
Q03164 (marker)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (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)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

6 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D003876 Dermatitis, Atopic C00005138
D012640 Seizures C00002218
D056486 Drug-Induced Liver Injury C00002576
D005234 Fatty Liver C00002576
D001145 Arrhythmias, Cardiac C00002236
D054537 Atrioventricular Block C00002236