Species

KNApSAcK Entry

Organism name Magnolia praecocissima
Genus Magnolia
Family Magnoliaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Magnolia praecocissima
Linked NCBI taxonomy ID 81865
Linked level species

Family

Family in NCBI taxonomy Magnoliaceae
ID 3401

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Magnoliophyta
ID 3398

Metabolite list (7)

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
C00033151 External link 512 Magnostellin B
/ (+)-Magnostellin B
No. 38 No. 21
C00000640 External link 512 (+)-Eudesmin
CHEMBL519099
CHEMBL512865
CHEMBL523743
CHEMBL464352
CHEMBL1726879
C105875
2 / 0 / 0 No. 38 No. 21
C00032559 External link 512 (-)-Fargesol
No. 38 No. 21
C00000643 External link 512 Kobusin
/ (+)-Kobusin
/ (+)-Spinescin
/ Methylpiperitol
CHEMBL462822
No. 38 No. 21
C00003345 External link 512 Parthenolide
CHEMBL363656
CHEMBL477923
CHEMBL388727
CHEMBL465158
CHEMBL540445
CHEMBL1356390
CHEMBL1527933
CHEMBL1601875
CHEMBL1881731
CHEMBL2142363
CHEMBL2357484
123 / 80 / 85 No. 227 No. 38
C00000601 External link 512 (+)-Sesamin
CHEMBL43469
CHEMBL252915
CHEMBL1572261
CHEMBL1591714
CHEMBL1708854
CHEMBL1904496
CHEMBL1968861
C054125
20 / 24 / 15 0 / 5 No. 621 No. 21
C00001259 External link 512 Naphthalene
CHEMBL16293
C031721
6 / 5 / 4 43 / 18 No. 5021

Human Protein / Gene in interactions

134 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
O75496 Geminin Unclassified protein C00000601 C00001259 C00003345 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00000601 C00003345 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00000601 C00003345 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00000601 C00003345 4 / 3
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000601 C00003345 0 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000601 C00003345 1 / 1
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000601 C00003345 0 / 1
Q9UBT6 DNA polymerase kappa Enzyme C00000640 C00003345 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00001259 C00003345 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00000601 C00003345 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00000601 C00003345 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000601 C00003345 1 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00000601 C00003345 2 / 0
P11509 Cytochrome P450 2A6 Cytochrome P450 2A6 C00001259 C00003345 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00000601 C00003345 2 / 3
Q13148 TAR DNA-binding protein 43 Unclassified protein C00000601 C00003345 1 / 1
P14780 Matrix metalloproteinase-9 M10A C00003345 2 / 2
P02545 Prelamin-A/C Unclassified protein C00003345 11 / 10
P16473 Thyrotropin receptor Glycohormone receptor C00003345 3 / 2
P42574 Caspase-3 C14 C00001259 0 / 0
P00918 Carbonic anhydrase 2 Lyase C00003345 1 / 2
P07550 Beta-2 adrenergic receptor Adrenergic receptor C00003345 0 / 1
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00003345 1 / 1
P25021 Histamine H2 receptor Histamine receptor C00003345 0 / 0
P35367 Histamine H1 receptor Histamine receptor C00003345 0 / 0
Q01959 Sodium-dependent dopamine transporter Dopamine C00003345 1 / 0
P08912 Muscarinic acetylcholine receptor M5 Acetylcholine receptor C00003345 0 / 0
P18825 Alpha-2C adrenergic receptor Adrenergic receptor C00003345 0 / 0
P13945 Beta-3 adrenergic receptor Adrenergic receptor C00003345 0 / 0
P25024 C-X-C chemokine receptor type 1 CXC chemokine receptor C00003345 0 / 0
P06241 Tyrosine-protein kinase Fyn Src C00003345 0 / 0
Q08209 Serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform Ser_Thr C00003345 0 / 0
P27361 Mitogen-activated protein kinase 3 Erk C00003345 0 / 0
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00003345 1 / 8
P17252 Protein kinase C alpha type Alpha C00003345 0 / 0
P14416 D(2) dopamine receptor Dopamine receptor C00003345 2 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00003345 0 / 0
P37288 Vasopressin V1a receptor Vasopressin and oxytocin receptor C00003345 0 / 0
P41145 Kappa-type opioid receptor Opioid receptor C00003345 0 / 0
Q9Y271 Cysteinyl leukotriene receptor 1 Leukotriene receptor C00003345 0 / 0
P29274 Adenosine receptor A2a Adenosine receptor C00003345 0 / 0
P25929 Neuropeptide Y receptor type 1 Neuropeptide Y receptor C00003345 0 / 0
P50052 Type-2 angiotensin II receptor Angiotensin receptor C00003345 1 / 1
O15296 Arachidonate 15-lipoxygenase B Enzyme C00000601 0 / 0
P17948 Vascular endothelial growth factor receptor 1 Vegfr C00003345 0 / 0
P41968 Melanocortin receptor 3 Melanocortin receptor C00003345 1 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00003345 0 / 0
P29466 Caspase-1 C14 C00003345 0 / 0
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00003345 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00000640 0 / 0
P42858 Huntingtin Unclassified protein C00003345 1 / 1
P49146 Neuropeptide Y receptor type 2 Neuropeptide Y receptor C00003345 0 / 0
Q16539 Mitogen-activated protein kinase 14 p38 C00003345 0 / 0
P51151 Ras-related protein Rab-9A Unclassified protein C00003345 0 / 0
P04035 3-hydroxy-3-methylglutaryl-coenzyme A reductase Oxidoreductase C00003345 0 / 0
P08913 Alpha-2A adrenergic receptor Adrenergic receptor C00003345 0 / 0
P21917 D(4) dopamine receptor Dopamine receptor C00003345 0 / 0
P30988 Calcitonin receptor Calcitonin receptor C00003345 0 / 0
P35462 D(3) dopamine receptor Dopamine receptor C00003345 1 / 0
P41143 Delta-type opioid receptor Opioid receptor C00003345 0 / 0
Q92731 Estrogen receptor beta NR3A2 C00003345 0 / 1
P41595 5-hydroxytryptamine receptor 2B Serotonin receptor C00003345 0 / 0
P25101 Endothelin-1 receptor Endothelin receptor C00003345 0 / 0
P30411 B2 bradykinin receptor Bradykinin receptor C00003345 0 / 0
P32245 Melanocortin receptor 4 Melanocortin receptor C00003345 1 / 0
P32238 Cholecystokinin receptor type A Cholecystokinin receptor C00003345 0 / 0
P08311 Cathepsin G S1A C00003345 0 / 0
Q99720 Sigma non-opioid intracellular receptor 1 Membrane receptor C00003345 1 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00000601 0 / 0
P03956 Interstitial collagenase M10A C00003345 0 / 1
P32241 Vasoactive intestinal polypeptide receptor 1 Vasoactive intestinal peptide receptor C00003345 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00000601 7 / 3
Q04206 Transcription factor p65 Transcription Factor C00003345 0 / 0
P42226 Signal transducer and activator of transcription 6 Unclassified protein C00003345 0 / 0
P33765 Adenosine receptor A3 Adenosine receptor C00003345 0 / 0
P11021 78 kDa glucose-regulated protein Unclassified protein C00003345 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00000601 0 / 0
P04150 Glucocorticoid receptor NR3C1 C00003345 0 / 1
P08172 Muscarinic acetylcholine receptor M2 Acetylcholine receptor C00003345 2 / 0
P11229 Muscarinic acetylcholine receptor M1 Acetylcholine receptor C00003345 0 / 0
P21554 Cannabinoid receptor 1 Cannabinoid receptor C00003345 0 / 0
P31645 Sodium-dependent serotonin transporter Serotonin C00003345 2 / 0
P04626 Receptor tyrosine-protein kinase erbB-2 TK tyrosine-protein kinase EGFR subfamily C00003345 5 / 9
P20309 Muscarinic acetylcholine receptor M3 Acetylcholine receptor C00003345 1 / 0
P21452 Substance-K receptor Neurokinin receptor C00003345 0 / 0
P51679 C-C chemokine receptor type 4 CC chemokine receptor C00003345 0 / 0
P51681 C-C chemokine receptor type 5 CC chemokine receptor C00003345 3 / 0
P50406 5-hydroxytryptamine receptor 6 Serotonin receptor C00003345 0 / 0
P18054 Arachidonate 12-lipoxygenase, 12S-type Enzyme C00001259 2 / 0
P41597 C-C chemokine receptor type 2 CC chemokine receptor C00003345 1 / 0
P08246 Neutrophil elastase S1A C00003345 2 / 1
P08575 Receptor-type tyrosine-protein phosphatase C Enzyme C00003345 2 / 1
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00003345 2 / 2
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00000601 2 / 2
O15118 Niemann-Pick C1 protein Unclassified protein C00003345 1 / 1
Q01453 Peripheral myelin protein 22 Unclassified protein C00003345 5 / 2
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00003345 0 / 3
O76074 cGMP-specific 3',5'-cyclic phosphodiesterase PDE_5A C00003345 0 / 0
P03372 Estrogen receptor NR3A1 C00003345 1 / 1
P08588 Beta-1 adrenergic receptor Adrenergic receptor C00003345 1 / 0
P21728 D(1A) dopamine receptor Dopamine receptor C00003345 0 / 0
P28223 5-hydroxytryptamine receptor 2A Serotonin receptor C00003345 0 / 0
P28335 5-hydroxytryptamine receptor 2C Serotonin receptor C00003345 0 / 0
P35372 Mu-type opioid receptor Opioid receptor C00003345 0 / 0
P08173 Muscarinic acetylcholine receptor M4 Acetylcholine receptor C00003345 0 / 0
P25103 Substance-P receptor Neurokinin receptor C00003345 0 / 0
P25105 Platelet-activating factor receptor PAF receptor C00003345 0 / 0
P33032 Melanocortin receptor 5 Melanocortin receptor C00003345 0 / 0
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor C00003345 0 / 0
P49798 Regulator of G-protein signaling 4 Unclassified protein C00003345 2 / 0
Q99700 Ataxin-2 Unclassified protein C00003345 1 / 1
P05181 Cytochrome P450 2E1 Cytochrome P450 2E1 C00003345 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00000601 0 / 0
Q16637 Survival motor neuron protein Unclassified protein C00000601 4 / 1
Q99549 M-phase phosphoprotein 8 Unclassified protein C00003345 0 / 0
P04637 Cellular tumor antigen p53 Transcription Factor C00003345 7 / 37
P10275 Androgen receptor NR3C4 C00001259 3 / 4
P23975 Sodium-dependent noradrenaline transporter Norepinephrine C00003345 1 / 1
P25100 Alpha-1D adrenergic receptor Adrenergic receptor C00003345 0 / 0
P30542 Adenosine receptor A1 Adenosine receptor C00003345 0 / 0
P18089 Alpha-2B adrenergic receptor Adrenergic receptor C00003345 0 / 0
P24557 Thromboxane-A synthase Cytochrome P450 5A1 C00003345 1 / 1
P06239 Tyrosine-protein kinase Lck Src C00003345 0 / 1
P25025 C-X-C chemokine receptor type 2 CXC chemokine receptor C00003345 0 / 0
P42345 Serine/threonine-protein kinase mTOR Enzyme C00003345 0 / 0
P40225 Thrombopoietin Unclassified protein C00003345 1 / 1
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00003345 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00003345 1 / 0
O00255 Menin Unclassified protein C00003345 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00003345 1 / 2
Q13951 Core-binding factor subunit beta Unclassified protein C00003345 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00003345 1 / 4
Q00653 Nuclear factor NF-kappa-B p100 subunit Transcription Factor C00003345 0 / 0
P22303 Acetylcholinesterase Hydrolase C00003345 1 / 0

43 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
5243 ABCB1, ABC20, CD243, CLCS, GP170, MDR1, P-GP, PGY1 ATP-binding cassette, sub-family B (MDR/TAP), member 1 (EC:3.6.3.44) C00001259
196 AHR, bHLHe76 aryl hydrocarbon receptor C00001259
429 ASCL1, ASH1, HASH1, MASH1, bHLHa46 achaete-scute family bHLH transcription factor 1 C00001259
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00001259
842 CASP9, APAF-3, APAF3, ICE-LAP6, MCH6, PPP1R56 caspase 9, apoptosis-related cysteine peptidase (EC:3.4.22.62) C00001259
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00001259
1544 CYP1A2, CP12, P3-450, P450(PA) cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) C00001259
1545 CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) C00001259
1557 CYP2C19, CPCJ, CYP2C, P450C2C, P450IIC19 cytochrome P450, family 2, subfamily C, polypeptide 19 (EC:1.14.13.48 1.14.13.49 1.14.13.80) C00001259
1558 CYP2C8, CPC8, CYPIIC8, MP-12/MP-20 cytochrome P450, family 2, subfamily C, polypeptide 8 (EC:1.14.14.1) C00001259
1559 CYP2C9, CPC9, CYP2C, CYP2C10, CYPIIC9, P450IIC9 cytochrome P450, family 2, subfamily C, polypeptide 9 (EC:1.14.13.48 1.14.13.49 1.14.13.80) C00001259
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) C00001259
1571 CYP2E1, CPE1, CYP2E, P450-J, P450C2E cytochrome P450, family 2, subfamily E, polypeptide 1 (EC:1.14.13.n7) C00001259
13107 C00001259
29785 CYP2S1 cytochrome P450, family 2, subfamily S, polypeptide 1 (EC:1.14.14.1) C00001259
1576 CYP3A4, CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4, HLP, NF-25, P450C3, P450PCN1 cytochrome P450, family 3, subfamily A, polypeptide 4 (EC:1.14.13.67 1.14.13.97 1.14.13.32 1.14.13.157) C00001259
1577 CYP3A5, CP35, CYPIIIA5, P450PCN3, PCN3 cytochrome P450, family 3, subfamily A, polypeptide 5 (EC:1.14.14.1) C00001259
2052 EPHX1, EPHX, EPOX, HYL1, MEH epoxide hydrolase 1, microsomal (xenobiotic) (EC:3.3.2.9) C00001259
2053 EPHX2, CEH, SEH epoxide hydrolase 2, cytoplasmic (EC:3.3.2.10 3.1.3.76) C00001259
2252 FGF7, HBGF-7, KGF fibroblast growth factor 7 C00001259
2353 FOS, AP-1, C-FOS, p55 FBJ murine osteosarcoma viral oncogene homolog C00001259
2521 FUS, ALS6, ETM4, FUS1, HNRNPP2, POMP75, TLS fused in sarcoma C00001259
2642 GCGR, GGR glucagon receptor C00001259
2944 GSTM1, GST1, GSTM1-1, GSTM1a-1a, GSTM1b-1b, GTH4, GTM1, H-B, MU, MU-1 glutathione S-transferase mu 1 (EC:2.5.1.18) C00001259
8870 IER3, DIF-2, DIF2, GLY96, IEX-1, IEX-1L, IEX1, PRG1 immediate early response 3 C00001259
3565 IL4, BCGF-1, BCGF1, BSF-1, BSF1, IL-4 interleukin 4 C00001259
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00001259
3725 JUN, AP-1, AP1, c-Jun jun proto-oncogene C00001259
3956 LGALS1, GAL1, GBP lectin, galactoside-binding, soluble, 1 C00001259
4157 MC1R, CMM5, MSH-R, SHEP2 melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor) C00001259
4159 MC3R, BMIQ9, MC3, MC3-R, OB20, OQTL melanocortin 3 receptor C00001259
4160 MC4R melanocortin 4 receptor C00001259
4161 MC5R, MC2 melanocortin 5 receptor C00001259
10403 NDC80, HEC, HEC1, HsHec1, KNTC2, TID3, hsNDC80 NDC80 kinetochore complex component C00001259
4846 NOS3, ECNOS, eNOS nitric oxide synthase 3 (endothelial cell) (EC:1.14.13.39) C00001259
5053 PAH, PH, PKU, PKU1 phenylalanine hydroxylase (EC:1.14.16.1) C00001259
5894 RAF1, CRAF, NS5, Raf-1, c-Raf v-raf-1 murine leukemia viral oncogene homolog 1 (EC:2.7.11.1) C00001259
389 RHOC, ARH9, ARHC, H9, RHOH9 ras homolog family member C C00001259
7356 SCGB1A1, CC10, CC16, CCPBP, CCSP, UGB, UP-1, UP1 secretoglobin, family 1A, member 1 (uteroglobin) C00001259
6855 SYP, MRXSYP synaptophysin C00001259
6932 TCF7, TCF-1 transcription factor 7 (T-cell specific, HMG-box) C00001259
7076 TIMP1, CLGI, EPA, EPO, HCI, TIMP TIMP metallopeptidase inhibitor 1 C00001259
7157 TP53, BCC7, LFS1, P53, TRP53 tumor protein p53 C00001259

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (96)

OMIM preferred title UniProt
#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
#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
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#602025 Body mass index quantitative trait locus 9; bmiq9 P41968
#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 P18054
P84022
#162800 Cyclic neutropenia P08246
#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
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#133239 Esophageal cancer P04637
P18054
#615363 Estrogen resistance; estrr P03372
#600274 Frontotemporal dementia; ftd P10636
#613659 Gastric cancer P04626
#137215 Gastric cancer, hereditary diffuse; hdgc P04626
#231095 Ghosal hematodiaphyseal dysplasia; ghdd P24557
#137800 Glioma susceptibility 1; glm1 O75874
P04626
#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
#143100 Huntington disease; hd P42858
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#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
#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
%300852 Mental retardation, x-linked 88; mrx88 P50052
#613073 Metaphyseal anadysplasia 2; mandp2 P14780
#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
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#159900 Myoclonic dystonia P14416
#162500 Neuropathy, hereditary, with liability to pressure palsies; hnpp Q01453
#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
#166350 Osseous heteroplasia, progressive; poh P63092
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#167000 Ovarian cancer P04626
#260500 Papilloma of choroid plexus; cpp P04637
#260540 Parkinson-dementia syndrome P10636
#613135 Parkinsonism-dystonia, infantile; pkdys Q01959
#172700 Pick disease of brain P10636
#102200 Pituitary adenoma, growth hormone-secreting P63092
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#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
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#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
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#187950 Thrombocythemia 1; thcyt1 P40225
#190300 Tremor, hereditary essential, 1; etm1 P35462
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#610379 West nile virus, susceptibility to P51681
#112100 Yt blood group antigen P22303

KEGG DISEASE (95)

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)
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)
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)
H00031 Breast cancer P04626 (related)
P04626 (marker)
P04637 (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)
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)
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)
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)
H00227 Congenital amegakaryocytic thrombocytopenia (CAMT) P40225 (marker)
H00059 Huntington's disease (HD) P42858 (related)
H00480 Non-syndromic X-linked mental retardation P50052 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
Q03164 (related)
Q03164 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00978 Thrombocytopenia (THC) Q01196 (related)
H01296 Hereditary neuropathy with liability to pressure palsies (HNPP) Q01453 (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)

Diseases related to CTD interactions

23 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D000014 Abnormalities, Drug-Induced C00001259
D058186 Acute Kidney Injury C00001259
D055371 Acute Lung Injury C00001259
D000743 Anemia, Hemolytic C00001259
D002386 Cataract C00001259
D006456 Hemoglobinuria C00001259
D006529 Hepatomegaly C00001259
D006959 Hyperoxaluria C00001259
D006965 Hyperplasia C00001259
D008114 Liver Neoplasms, Experimental C00001259
D055370 Lung Injury C00001259
D008175 Lung Neoplasms C00001259
D048629 Micronuclei, Chromosome-Defective C00001259
D009336 Necrosis C00001259
D009362 Neoplasm Metastasis C00001259
D011041 Poisoning C00001259
D014133 Tracheal Diseases C00001259
D015431 Weight Loss C00001259
D001930 Brain Injuries C00000601
D002375 Catalepsy C00000601
D018476 Hypokinesia C00000601
D020244 Infarction, Middle Cerebral Artery C00000601
D020734 Parkinsonian Disorders C00000601