Species

KNApSAcK Entry

Organism name Illicium fargesii
Genus Illicium
Family Illiciaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Illicium fargesii
Linked NCBI taxonomy ID 124774
Linked level species

Family

Family in NCBI taxonomy Schisandraceae
ID 16733

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Magnoliophyta
ID 3398

Metabolite list (10)

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
C00003212 External link 512 Anisatin
CHEMBL220362
CHEMBL517697
1 / 2 / 2 No. 680 No. 38
C00002609 External link 512 Hinokiol
/ (+)-Hinokiol
CHEMBL16901
26 / 24 / 20 No. 761 No. 23
C00000591 External link 512 Magnolol
CHEMBL180920
C005498
21 / 17 / 15 1 / 7 No. 761 No. 23
C00029961 External link 512 Cinnamic acid
/ .beta-Phenylacrylic acid
CHEMBL27246
C029010
5 / 2 / 2 16 / 2 No. 904 No. 6
C00002644 External link 512 Catechol
/ Pyrocatechol
CHEMBL280998
C034221
148 / 82 / 64 22 / 5 No. 1590 No. 82
C00029459 External link 512 2-Methoxyphenol
CHEMBL13766
D006139
15 / 18 / 47 3 / 1 No. 2352
C00030514 External link 512 Integrifoliolin
No. 2496
C00030124 External link 512 Dictagymnin
No. 2759
C00000592 External link 512 Isomagnolol
CHEMBL183320
No. 3309
C00030704 External link 512 Macranthol
/ (+)-Macranthol
No. 6572

Human Protein / Gene in interactions

172 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q99700 Ataxin-2 Unclassified protein C00000591 C00002609 C00002644 1 / 1
O75496 Geminin Unclassified protein C00000591 C00002609 C00002644 0 / 0
P14780 Matrix metalloproteinase-9 M10A C00002644 C00003212 C00029459 2 / 2
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00000591 C00002644 C00029459 0 / 0
P21554 Cannabinoid receptor 1 Cannabinoid receptor C00000591 C00002609 C00002644 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00000591 C00002609 C00002644 4 / 3
P09917 Arachidonate 5-lipoxygenase Oxidoreductase C00002609 C00002644 C00029459 0 / 0
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00002609 C00002644 5 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00002644 C00029459 0 / 0
Q9GZV3 High affinity choline transporter 1 Choline Na-symporter C00000591 C00002609 1 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00002609 C00002644 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00002609 C00002644 0 / 0
P03372 Estrogen receptor NR3A1 C00002644 C00029961 1 / 1
P51449 Nuclear receptor ROR-gamma Nuclear hormone receptor subfamily 1 group F member 3 C00002644 C00029459 0 / 0
P06746 DNA polymerase beta Enzyme C00002609 C00002644 0 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00000591 C00002644 2 / 2
P10253 Lysosomal alpha-glucosidase Hydrolase C00000591 C00002609 1 / 1
P08253 72 kDa type IV collagenase M10A C00002644 C00029459 1 / 3
P08254 Stromelysin-1 M10A C00002644 C00029459 1 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00000591 C00002644 0 / 0
P22894 Neutrophil collagenase M10A C00002644 C00029459 0 / 0
P11021 78 kDa glucose-regulated protein Unclassified protein C00002609 C00002644 0 / 0
P03956 Interstitial collagenase M10A C00002644 C00029459 0 / 1
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00000591 C00002609 0 / 0
P00915 Carbonic anhydrase 1 Lyase C00002644 C00029459 0 / 0
O00255 Menin Unclassified protein C00000591 C00002609 2 / 5
Q9Y2T6 G-protein coupled receptor 55 Lysophosphatidylinositol receptor C00000591 C00002609 0 / 0
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00000591 C00002609 1 / 2
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00000591 C00002609 2 / 0
P39748 Flap endonuclease 1 Enzyme C00002609 C00002644 0 / 0
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00002644 C00029961 1 / 1
P00352 Retinal dehydrogenase 1 Enzyme C00000591 C00002644 0 / 0
P00918 Carbonic anhydrase 2 Lyase C00002644 C00029459 1 / 2
O15296 Arachidonate 15-lipoxygenase B Enzyme C00000591 C00002644 0 / 0
P34972 Cannabinoid receptor 2 Cannabinoid receptor C00000591 C00002609 0 / 0
P14867 Gamma-aminobutyric acid receptor subunit alpha-1 GABA-A alpha C00000591 C00002609 1 / 1
P47870 Gamma-aminobutyric acid receptor subunit beta-2 GABA-A beta C00000591 C00002609 0 / 0
P22303 Acetylcholinesterase Hydrolase C00002644 1 / 0
P08912 Muscarinic acetylcholine receptor M5 Acetylcholine receptor C00002644 0 / 0
P18825 Alpha-2C adrenergic receptor Adrenergic receptor C00002644 0 / 0
P13945 Beta-3 adrenergic receptor Adrenergic receptor C00002644 0 / 0
P25024 C-X-C chemokine receptor type 1 CXC chemokine receptor C00002644 0 / 0
P06241 Tyrosine-protein kinase Fyn Src C00002644 0 / 0
Q08209 Serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform Ser_Thr C00002644 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00002644 0 / 1
P35367 Histamine H1 receptor Histamine receptor C00002644 0 / 0
P25021 Histamine H2 receptor Histamine receptor C00002644 0 / 0
Q9GZT9 Egl nine homolog 1 Enzyme C00002644 1 / 1
P54132 Bloom syndrome protein Enzyme C00002644 1 / 2
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00002644 1 / 8
P14416 D(2) dopamine receptor Dopamine receptor C00002644 2 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00002644 0 / 0
P37288 Vasopressin V1a receptor Vasopressin and oxytocin receptor C00002644 0 / 0
P41145 Kappa-type opioid receptor Opioid receptor C00002644 0 / 0
Q9Y271 Cysteinyl leukotriene receptor 1 Leukotriene receptor C00002644 0 / 0
P29274 Adenosine receptor A2a Adenosine receptor C00002644 0 / 0
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00002644 1 / 1
P23280 Carbonic anhydrase 6 Lyase C00002644 0 / 0
P25929 Neuropeptide Y receptor type 1 Neuropeptide Y receptor C00002644 0 / 0
P50052 Type-2 angiotensin II receptor Angiotensin receptor C00002644 1 / 1
P07550 Beta-2 adrenergic receptor Adrenergic receptor C00002644 0 / 1
P17948 Vascular endothelial growth factor receptor 1 Vegfr C00002644 0 / 0
P41968 Melanocortin receptor 3 Melanocortin receptor C00002644 1 / 0
Q9ULX7 Carbonic anhydrase 14 Lyase C00002644 0 / 0
P19793 Retinoic acid receptor RXR-alpha NR2B1 C00002609 0 / 0
P17405 Sphingomyelin phosphodiesterase Enzyme C00002609 2 / 2
O43570 Carbonic anhydrase 12 Lyase C00002644 1 / 2
P11509 Cytochrome P450 2A6 Cytochrome P450 2A6 C00002644 0 / 0
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00002644 0 / 0
Q8TDS4 Hydroxycarboxylic acid receptor 2 Hydroxycarboxylic acid receptor C00029961 0 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00029459 3 / 2
P37840 Alpha-synuclein Unclassified protein C00002609 4 / 2
P02545 Prelamin-A/C Unclassified protein C00002644 11 / 10
P51151 Ras-related protein Rab-9A Unclassified protein C00002644 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00002644 0 / 0
P04035 3-hydroxy-3-methylglutaryl-coenzyme A reductase Oxidoreductase C00002644 0 / 0
P08913 Alpha-2A adrenergic receptor Adrenergic receptor C00002644 0 / 0
P21917 D(4) dopamine receptor Dopamine receptor C00002644 0 / 0
P30988 Calcitonin receptor Calcitonin receptor C00002644 0 / 0
P35462 D(3) dopamine receptor Dopamine receptor C00002644 1 / 0
P41143 Delta-type opioid receptor Opioid receptor C00002644 0 / 0
Q92731 Estrogen receptor beta NR3A2 C00002644 0 / 1
P41595 5-hydroxytryptamine receptor 2B Serotonin receptor C00002644 0 / 0
P15121 Aldose reductase Enzyme C00029961 0 / 0
P25101 Endothelin-1 receptor Endothelin receptor C00002644 0 / 0
P30411 B2 bradykinin receptor Bradykinin receptor C00002644 0 / 0
P10145 Interleukin-8 Secreted protein C00002644 0 / 0
P32245 Melanocortin receptor 4 Melanocortin receptor C00002644 1 / 0
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00002609 0 / 0
P32238 Cholecystokinin receptor type A Cholecystokinin receptor C00002644 0 / 0
P08311 Cathepsin G S1A C00002644 0 / 0
Q99720 Sigma non-opioid intracellular receptor 1 Membrane receptor C00002644 1 / 0
P27361 Mitogen-activated protein kinase 3 Erk C00002644 0 / 0
P17252 Protein kinase C alpha type Alpha C00002644 0 / 0
P32241 Vasoactive intestinal polypeptide receptor 1 Vasoactive intestinal peptide receptor C00002644 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00002644 1 / 1
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00002644 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00002644 0 / 0
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme C00002644 0 / 0
P29466 Caspase-1 C14 C00002644 0 / 0
P04150 Glucocorticoid receptor NR3C1 C00002644 0 / 1
P08172 Muscarinic acetylcholine receptor M2 Acetylcholine receptor C00002644 2 / 0
P11229 Muscarinic acetylcholine receptor M1 Acetylcholine receptor C00002644 0 / 0
P43166 Carbonic anhydrase 7 Lyase C00002644 0 / 0
P31645 Sodium-dependent serotonin transporter Serotonin C00002644 2 / 0
P35218 Carbonic anhydrase 5A, mitochondrial Lyase C00002644 0 / 0
P04626 Receptor tyrosine-protein kinase erbB-2 TK tyrosine-protein kinase EGFR subfamily C00002644 5 / 9
P20309 Muscarinic acetylcholine receptor M3 Acetylcholine receptor C00002644 1 / 0
P21452 Substance-K receptor Neurokinin receptor C00002644 0 / 0
P51679 C-C chemokine receptor type 4 CC chemokine receptor C00002644 0 / 0
P51681 C-C chemokine receptor type 5 CC chemokine receptor C00002644 3 / 0
P50406 5-hydroxytryptamine receptor 6 Serotonin receptor C00002644 0 / 0
Q96RI1 Bile acid receptor NR1H4 C00002644 0 / 0
Q13133 Oxysterols receptor LXR-alpha NR1H3 C00002609 0 / 0
P41597 C-C chemokine receptor type 2 CC chemokine receptor C00002644 1 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00002644 0 / 0
P08575 Receptor-type tyrosine-protein phosphatase C Enzyme C00002644 2 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00002644 0 / 0
Q16790 Carbonic anhydrase 9 Lyase C00002644 0 / 1
Q9Y2D0 Carbonic anhydrase 5B, mitochondrial Lyase C00002644 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00002644 3 / 3
P49146 Neuropeptide Y receptor type 2 Neuropeptide Y receptor C00002644 0 / 0
O15118 Niemann-Pick C1 protein Unclassified protein C00002644 1 / 1
Q01453 Peripheral myelin protein 22 Unclassified protein C00002644 5 / 2
Q16539 Mitogen-activated protein kinase 14 p38 C00002644 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00029459 0 / 0
O76074 cGMP-specific 3',5'-cyclic phosphodiesterase PDE_5A C00002644 0 / 0
P33765 Adenosine receptor A3 Adenosine receptor C00002644 0 / 0
P08588 Beta-1 adrenergic receptor Adrenergic receptor C00002644 1 / 0
Q01959 Sodium-dependent dopamine transporter Dopamine C00002644 1 / 0
P28223 5-hydroxytryptamine receptor 2A Serotonin receptor C00002644 0 / 0
P28335 5-hydroxytryptamine receptor 2C Serotonin receptor C00002644 0 / 0
P35372 Mu-type opioid receptor Opioid receptor C00002644 0 / 0
P08173 Muscarinic acetylcholine receptor M4 Acetylcholine receptor C00002644 0 / 0
P25103 Substance-P receptor Neurokinin receptor C00002644 0 / 0
P25105 Platelet-activating factor receptor PAF receptor C00002644 0 / 0
P33032 Melanocortin receptor 5 Melanocortin receptor C00002644 0 / 0
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor C00002644 0 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme C00002644 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00002644 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002644 0 / 1
P05181 Cytochrome P450 2E1 Cytochrome P450 2E1 C00002644 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00002644 0 / 0
Q6W5P4 Neuropeptide S receptor Neuropeptide receptor C00000591 1 / 0
P08246 Neutrophil elastase S1A C00002644 2 / 1
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00002644 2 / 2
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00002644 0 / 3
Q99549 M-phase phosphoprotein 8 Unclassified protein C00002644 0 / 0
P21728 D(1A) dopamine receptor Dopamine receptor C00002644 0 / 0
P10275 Androgen receptor NR3C4 C00029459 3 / 4
P23975 Sodium-dependent noradrenaline transporter Norepinephrine C00002644 1 / 1
P25100 Alpha-1D adrenergic receptor Adrenergic receptor C00002644 0 / 0
P30542 Adenosine receptor A1 Adenosine receptor C00002644 0 / 0
P18089 Alpha-2B adrenergic receptor Adrenergic receptor C00002644 0 / 0
P24557 Thromboxane-A synthase Cytochrome P450 5A1 C00002644 1 / 1
P07451 Carbonic anhydrase 3 Lyase C00002644 0 / 0
P06239 Tyrosine-protein kinase Lck Src C00002644 0 / 1
P25025 C-X-C chemokine receptor type 2 CXC chemokine receptor C00002644 0 / 0
P49798 Regulator of G-protein signaling 4 Unclassified protein C00002644 2 / 0
P22748 Carbonic anhydrase 4 Lyase C00002644 1 / 1
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00002644 1 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00002644 0 / 0
Q16637 Survival motor neuron protein Unclassified protein C00002644 4 / 1
P46063 ATP-dependent DNA helicase Q1 Enzyme C00002644 0 / 0
P40225 Thrombopoietin Unclassified protein C00002644 1 / 1
P04637 Cellular tumor antigen p53 Transcription Factor C00029459 7 / 37
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00002644 1 / 1
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00002644 1 / 0
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00029961 0 / 0
P42345 Serine/threonine-protein kinase mTOR Enzyme C00002644 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00002644 0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00000591 1 / 1

41 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
1571 CYP2E1, CPE1, CYP2E, P450-J, P450C2E cytochrome P450, family 2, subfamily E, polypeptide 1 (EC:1.14.13.n7) C00002644 C00029961
6356 CCL11, SCYA11 chemokine (C-C motif) ligand 11 C00002644
1548 CYP2A6, CPA6, CYP2A, CYP2A3, CYPIIA6, P450C2A, P450PB cytochrome P450, family 2, subfamily A, polypeptide 6 (EC:1.14.14.1) C00029961
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) C00029961
1558 CYP2C8, CPC8, CYPIIC8, MP-12/MP-20 cytochrome P450, family 2, subfamily C, polypeptide 8 (EC:1.14.14.1) C00029961
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) C00029961
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) C00029961
5468 PPARG, CIMT1, GLM1, NR1C3, PPARG1, PPARG2, PPARgamma peroxisome proliferator-activated receptor gamma C00000591
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) C00029961
338442 HCAR2, GPR109A, HCA2, HM74a, HM74b, NIACR1, PUMAG, Puma-g hydroxycarboxylic acid receptor 2 C00029961
3284 HSD3B2, HSD3B, HSDB, SDR11E2 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 (EC:1.1.1.145 5.3.3.1) C00029961
4846 NOS3, ECNOS, eNOS nitric oxide synthase 3 (endothelial cell) (EC:1.14.13.39) C00029961
7299 TYR, ATN, CMM8, OCA1, OCA1A, OCAIA, SHEP3 tyrosinase (EC:1.14.18.1) C00029961
54575 UGT1A10, UDPGT, UGT-1J, UGT1-10, UGT1.10, UGT1J UDP glucuronosyltransferase 1 family, polypeptide A10 (EC:2.4.1.17) C00029961
54659 UGT1A3, UDPGT, UDPGT_1-3, UGT-1C, UGT1-03, UGT1.3, UGT1C UDP glucuronosyltransferase 1 family, polypeptide A3 (EC:2.4.1.17) C00029961
54577 UGT1A7, UDPGT, UDPGT_1-7, UGT-1G, UGT1-07, UGT1.7, UGT1G UDP glucuronosyltransferase 1 family, polypeptide A7 (EC:2.4.1.17) C00029961
54576 UGT1A8, UDPGT, UDPGT_1-8, UGT-1H, UGT1-08, UGT1.8, UGT1A8S, UGT1H UDP glucuronosyltransferase 1 family, polypeptide A8 (EC:2.4.1.17) C00029961
212 ALAS2, ALAS-E, ALASE, ANH1, ASB, XLDPP, XLEPP, XLSA aminolevulinate, delta-, synthase 2 (EC:2.3.1.37) C00002644
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00002644
840 CASP7, CASP-7, CMH-1, ICE-LAP3, LICE2, MCH3 caspase 7, apoptosis-related cysteine peptidase (EC:3.4.22.60) C00002644
1586 CYP17A1, CPT7, CYP17, P450C17, S17AH cytochrome P450, family 17, subfamily A, polypeptide 1 (EC:1.14.99.9 4.1.2.30) C00029961
6347 CCL2, GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1, SCYA2, SMC-CF chemokine (C-C motif) ligand 2 C00002644
6348 CCL3, G0S19-1, LD78ALPHA, MIP-1-alpha, MIP1A, SCYA3 chemokine (C-C motif) ligand 3 C00002644
6351 CCL4, ACT2, AT744.1, G-26, HC21, LAG-1, LAG1, MIP-1-beta, MIP1B, MIP1B1, SCYA2, SCYA4 chemokine (C-C motif) ligand 4 C00002644
6352 CCL5, D17S136E, RANTES, SCYA5, SIS-delta, SISd, TCP228, eoCP chemokine (C-C motif) ligand 5 C00002644
1312 COMT catechol-O-methyltransferase (EC:2.1.1.6) C00002644
2623 GATA1, ERYF1, GATA-1, GF-1, GF1, NF-E1, NFE1, XLANP, XLTDA, XLTT GATA binding protein 1 (globin transcription factor 1) C00002644
3043 HBB, CD113t-C, beta-globin hemoglobin, beta C00002644
3145 HMBS, PBG-D, PBGD, PORC, UPS hydroxymethylbilane synthase (EC:2.5.1.61) C00002644
3586 IL10, CSIF, GVHDS, IL-10, IL10A, TGIF interleukin 10 C00002644
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00002644
4609 MYC, MRTL, MYCC, bHLHe39, c-Myc v-myc avian myelocytomatosis viral oncogene homolog C00002644
1728 NQO1, DHQU, DIA4, DTD, NMOR1, NMORI, QR1 NAD(P)H dehydrogenase, quinone 1 (EC:1.6.5.2) C00002644
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) C00002644
6799 SULT1A2, HAST4, P-PST, ST1A2, STP2, TSPST2 sulfotransferase family, cytosolic, 1A, phenol-preferring, member 2 (EC:2.8.2.1) C00002644
6818 SULT1A3, HAST, HAST3, M-PST, ST1A3/ST1A4, ST1A5, STM, TL-PST sulfotransferase family, cytosolic, 1A, phenol-preferring, member 3 (EC:2.8.2.1) C00002644
6819 SULT1C2, ST1C1, ST1C2, SULT1C1, humSULTC2 sulfotransferase family, cytosolic, 1C, member 2 (EC:2.8.2.-) C00002644
7037 TFRC, CD71, T9, TFR, TFR1, TR, TRFR, p90 transferrin receptor C00002644
213 ALB, PRO0883, PRO0903, PRO1341 albumin C00029459
759 CA1, CA-I, CAB, Car1 carbonic anhydrase I (EC:4.2.1.1) C00029459
760 CA2, CA-II, CAC, CAII, Car2 carbonic anhydrase II (EC:4.2.1.1) C00029459

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (110)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#100100 Abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism P20309
#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
#608584 Asthma-related traits, susceptibility to, 2 Q6W5P4
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#210900 Bloom syndrome; blm P54132
#602025 Body mass index quantitative trait locus 9; bmiq9 P41968
%606641 Body mass index; bmi P37231
#300615 Brunner syndrome P21397
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#609338 Carotid intimal medial thickness 1 P37231
#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
#614466 Coronary heart disease, susceptibility to, 6; chds6 P08254
#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
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#611136 Epilepsy, juvenile myoclonic, susceptibility to, 5; ejm5 P14867
#609820 Erythrocytosis, familial, 3; ecyt3 Q9GZT9
#133239 Esophageal cancer P04637
#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
P37231
#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
#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
#603932 Intervertebral disc disease; idd P14780
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#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
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#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
#259600 Multicentric osteolysis, nodulosis, and arthropathy; mona P08253
#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
#158580 Neuronopathy, distal hereditary motor, type viia; hmn7a Q9GZV3
#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
#601665 Obesity P32245
P37231
#164230 Obsessive-compulsive disorder; ocd P31645
#604715 Orthostatic intolerance P23975
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#167000 Ovarian cancer P04626
#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
#607276 Resting heart rate, variation in P08588
#275210 Restrictive dermopathy, lethal P02545
#600852 Retinitis pigmentosa 17; rp17 P22748
#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
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#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
#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 (103)

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)
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)
P08253 (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)
P37231 (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)
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)
P08253 (related)
P14780 (related)
P35354 (related)
H00029 Vulvar cancer P04637 (related)
H00032 Thyroid cancer P04637 (related)
P37231 (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)
H00093 Combined immunodeficiencies (CIDs) P06239 (related)
H00079 Asthma P07550 (related)
H00100 Neutropenic disorders P08246 (related)
H00472 Torg-Winchester syndrome P08253 (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)
H01205 Coumarin resistance P11712 (related)
H00479 Metaphyseal dysplasias P14780 (related)
H00808 Idiopathic generalized epilepsies (IGEs) P14867 (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)
H00527 Retinitis pigmentosa (RP) P22748 (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)
H00057 Parkinson's disease (PD) P37840 (related)
H00066 Lewy body dementia (LBD) P37840 (related)
H00227 Congenital amegakaryocytic thrombocytopenia (CAMT) P40225 (marker)
H00192 Xanthinuria P47989 (related)
H00480 Non-syndromic X-linked mental retardation P50052 (related)
Q99714 (related)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (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)
H00455 Spinal muscular atrophy (SMA) Q16637 (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)
H00236 Congenital polycythemia Q9GZT9 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

15 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D002545 Brain Ischemia C00000591
D056486 Drug-Induced Liver Injury C00000591
D005334 Fever C00000591
D018883 Heat Stroke C00000591
D009203 Myocardial Infarction C00000591
D017180 Tachycardia, Ventricular C00000591
D014693 Ventricular Fibrillation C00000591
D003384 Coxsackievirus Infections C00029961
D008545 Melanoma C00029961
D002869 Chromosome Aberrations C00002644
D048629 Micronuclei, Chromosome-Defective C00002644
D009784 Occupational Diseases C00002644
D011041 Poisoning C00002644
D012640 Seizures C00002644
D010146 Pain C00029459