Species

KNApSAcK Entry

Organism name Pterocarpus santalinus
Genus Pterocarpus
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Pterocarpus santalinus
Linked NCBI taxonomy ID 1071199
Linked level species

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

Natural Activity

List (19)

Species Activity
Pterocarpus santalinus L. f. Alexeteric
Pterocarpus santalinus L. f. Analgesic
Pterocarpus santalinus L. f. Anticonvulsant
Pterocarpus santalinus L. f. Antidiabetic
Pterocarpus santalinus L. f. Antiexudative
Pterocarpus santalinus L. f. Antipyretic
Pterocarpus santalinus L. f. Antispasmodic
Pterocarpus santalinus L. f. Aphrodisiac
Pterocarpus santalinus L. f. Astringent
Pterocarpus santalinus L. f. CNS Depressant
Pterocarpus santalinus L. f. Depurative
Pterocarpus santalinus L. f. Diaphoretic
Pterocarpus santalinus L. f. Expectorant
Pterocarpus santalinus L. f. Fungicide
Pterocarpus santalinus L. f. Hypoglycemic
Pterocarpus santalinus L. f. Insecticide
Pterocarpus santalinus L. f. Nematicide
Pterocarpus santalinus L. f. Tonic
Pterocarpus santalinus L. f. Tranquilizer

Metabolite list (29)

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
C00019424 External link 512 5,3',4'-Trihydroxy-7-methoxyisoflavone 3'-O-glucoside
No. 2 No. 15
C00009459 External link 512 Santal
/ 5,3',4'-Trihydroxy-7-methoxyisoflavone
No. 3 No. 15
C00036622 External link 512 6-Hydroxy-7,2',4',5'-tetramethoxyisoflavone
No. 8 No. 15
C00019047 External link 512 6-Hydroxy-7,2',4',5'-tetramethoxyisoflavone
No. 8 No. 15
C00019065 External link 512 Erythrodiol
/ 3beta-Erythrodiol
CHEMBL298604
CHEMBL60687
CHEMBL400074
C077953
4 / 0 / 1 No. 13 No. 51
C00049120 External link 512 beta-Amyrone
CHEMBL461060
No. 13 No. 51
C00003738 External link 512 beta-Amyrin
/ beta-Amirin
/ beta-Amyrine
/ beta-Amyrenol
C036380
0 / 4 No. 23 No. 51
C00029492 External link 512 epi-Lupeol
/ 3-Epilupeol
/ (+)-epi-Lupeol
CHEMBL289191
CHEMBL459702
3 / 0 / 0 No. 23 No. 51
C00003740 External link 512 Betulin
CHEMBL23236
CHEMBL140040
CHEMBL1610940
CHEMBL2000891
CHEMBL2069124
C002503
18 / 16 / 17 0 / 2 No. 23 No. 51
C00003749 External link 512 Lupeol
/ Lupenol
/ (+)-Lupenol
CHEMBL289191
CHEMBL459702
C010480
3 / 0 / 0 2 / 6 No. 23 No. 51
C00019220 External link 512 Lupenone
CHEMBL486393
CHEMBL575188
3 / 4 / 2 No. 23 No. 51
C00049211 External link 512 Lup-20(29)-ene-2alpha,3beta-diol
CHEMBL1773216
No. 23 No. 51
C00019435 External link 512 4',5-Dihydroxy-7-methoxyisoflavone 3'-O-(3''-E-cinnamoylglucoside)
No. 30 No. 15
C00023774 External link 512 Fucostanol
/ Stigmasterol
/ Dihydro-beta-sitosterol
/ (24S)24-Ethylcholestain-3beta-ol
CHEMBL66943
CHEMBL186373
CHEMBL400247
CHEMBL1568947
D013265
5 / 0 / 0 1 / 0 No. 53 No. 11
C00003672 External link 512 Sitosterol
/ beta-sitosterl
/ (-)-beta-Sitosterol
/ Stigmast-5-en-3beta-ol
CHEMBL221542
CHEMBL1398443
CHEMBL1875388
17 / 19 / 12 No. 53 No. 11
C00006925 External link 512 Isoliquiritigenin
CHEMBL129795
CHEMBL1395334
C040920
59 / 83 / 90 12 / 3 No. 92 No. 13
C00011147 External link 512 6,4'-Dihydroxyaurone 4-O-rutinoside
No. 169 No. 13
C00014665 External link 512 6,4'-Dihydroxyaurone-4-O-neohesperidoside
No. 169 No. 13
C00002902 External link 512 Pterostilbene
/ 3,5-Dimethoxy-4'-hydroxystilbene
CHEMBL87712
CHEMBL83527
C107773
19 / 19 / 20 54 / 15 No. 344 No. 13
C00012772 External link 512 Pterocarpdiolone
/ [4R-(4alpha,4aalpha,6beta,8abeta)]-Octahydro-4-hydroxy-6-(1-hydroxy-1-methylethyl)-4,8a-dimethyl-2(1H)-naphthalenone
No. 351
C00012771 External link 512 Pterocarptriol
/ [1R-(1alpha,3alpha,4abeta,7beta,8aalpha)]-Decahydro-7-(1-hydroxy-1-methylethyl)-1,4a-dimethyl-1,3-naphthalenediol
No. 351
C00000856 External link 512 4-Hydroxybenzoic acid
/ p-Hydroxybenzoic acid
CHEMBL441343
C038193
21 / 7 / 16 2 / 1 No. 817 No. 81
C00002648 External link 512 Gentisic acid
/ 2,5-Dihydroxybenzoic acid
CHEMBL1461
C010925
15 / 6 / 8 2 / 1 No. 817 No. 81
C00002624 External link 512 Savinin
/ (-)-Savinin
/ (-)-Hibalactone
CHEMBL395263
CHEMBL459851
7 / 10 / 5 No. 1029 No. 21
C00002682 External link 512 Vanillic acid
/ 3-Methoxy-4-hydroxybenzoic acid
CHEMBL120568
D014641
5 / 3 / 3 5 / 0 No. 1073
C00002776 External link 512 Sinapic acid
CHEMBL109341
C073734
5 / 5 / 5 0 / 5 No. 1366 No. 6
C00011146 External link 512 6-Hydroxy-5-methyl-3',4',5'-trimethoxyaurone-4-O-alpha-L-rhamnopyranoside
No. 3026
C00014668 External link 512 6-Hydroxy-7-methyl-3',4',5'-trimethoxyaurone 4-O-rhamnoside
No. 3026
C00012855 External link 512 Isopterocarpolone
/ [4aR-(4aalpha,6beta,8abeta)]-4a,5,6,7,8,8a-Hexahydro-6-(1-hydroxy-1-methylethyl)-4,8a-dimethyl-2(1H)-naphthalenone
No. 3519

Human Protein / Gene in interactions

124 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00002648 C00003672 C00003740 C00006925 C00019065 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00002624 C00002648 C00002682 C00006925 0 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00002776 C00002902 C00003740 C00006925 0 / 3
P11388 DNA topoisomerase 2-alpha Isomerase C00003740 C00003749 C00023774 C00029492 0 / 0
P08047 Transcription factor Sp1 Unclassified protein C00003672 C00003749 C00029492 0 / 0
P15121 Aldose reductase Enzyme C00002682 C00006925 C00019065 0 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00002776 C00002902 C00006925 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00003672 C00003740 C00006925 1 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00003672 C00003740 C00006925 0 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00003672 C00003740 C00006925 1 / 1
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00002624 C00002902 C00006925 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00003672 C00003740 C00006925 0 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00003672 C00003740 C00006925 0 / 0
P11387 DNA topoisomerase 1 Isomerase C00003740 C00003749 C00029492 0 / 0
P06746 DNA polymerase beta Enzyme C00003672 C00023774 0 / 0
Q16790 Carbonic anhydrase 9 Lyase C00000856 C00002648 0 / 1
P03372 Estrogen receptor NR3A1 C00002682 C00003672 1 / 1
P28482 Mitogen-activated protein kinase 1 Erk C00002902 C00006925 0 / 0
Q96RI1 Bile acid receptor NR1H4 C00003740 C00019220 0 / 0
P14679 Tyrosinase Oxidoreductase C00003672 C00019220 4 / 2
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00000856 C00006925 1 / 8
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00003740 C00006925 0 / 0
P14780 Matrix metalloproteinase-9 M10A C00002648 C00006925 2 / 2
P83916 Chromobox protein homolog 1 Unclassified protein C00002648 C00006925 0 / 0
Q8TDU6 G-protein coupled bile acid receptor 1 Steroid-like ligand receptor C00003740 C00019220 0 / 0
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002902 C00006925 1 / 2
P02545 Prelamin-A/C Unclassified protein C00003740 C00006925 11 / 10
P51580 Thiopurine S-methyltransferase Enzyme C00000856 C00002682 1 / 1
P10636 Microtubule-associated protein tau Unclassified protein C00002902 C00006925 4 / 3
P00915 Carbonic anhydrase 1 Lyase C00000856 C00002648 0 / 0
Q99700 Ataxin-2 Unclassified protein C00002624 C00006925 1 / 1
O75496 Geminin Unclassified protein C00002902 C00006925 0 / 0
O43570 Carbonic anhydrase 12 Lyase C00000856 C00002648 1 / 2
P00918 Carbonic anhydrase 2 Lyase C00000856 C00002648 1 / 2
Q9ULX7 Carbonic anhydrase 14 Lyase C00000856 C00002648 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00002624 C00006925 0 / 0
P08183 Multidrug resistance protein 1 drug C00002902 C00003672 1 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00002624 C00006925 1 / 0
O00255 Menin Unclassified protein C00002902 C00006925 2 / 5
P43166 Carbonic anhydrase 7 Lyase C00000856 C00002648 0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00002624 C00002902 1 / 1
Q9HAW7 UDP-glucuronosyltransferase 1-7 Enzyme C00000856 0 / 0
P54132 Bloom syndrome protein Enzyme C00006925 1 / 2
Q9UQ49 Sialidase-3 Enzyme C00000856 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00006925 2 / 3
Q02156 Protein kinase C epsilon type Eta C00003740 0 / 0
P23280 Carbonic anhydrase 6 Lyase C00000856 0 / 0
P34969 5-hydroxytryptamine receptor 7 Serotonin receptor C00023774 0 / 0
P17405 Sphingomyelin phosphodiesterase Enzyme C00002776 2 / 2
P51649 Succinate-semialdehyde dehydrogenase, mitochondrial Oxidoreductase C00000856 1 / 1
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00003740 0 / 0
P39748 Flap endonuclease 1 Enzyme C00006925 0 / 0
P42858 Huntingtin Unclassified protein C00002682 1 / 1
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00006925 2 / 0
P10828 Thyroid hormone receptor beta NR1A2 C00003740 3 / 1
P51151 Ras-related protein Rab-9A Unclassified protein C00002902 0 / 0
O60656 UDP-glucuronosyltransferase 1-9 Enzyme C00000856 0 / 0
P38398 Breast cancer type 1 susceptibility protein Enzyme C00002902 4 / 2
P16473 Thyrotropin receptor Glycohormone receptor C00003672 3 / 2
P37840 Alpha-synuclein Unclassified protein C00006925 4 / 2
P49841 Glycogen synthase kinase-3 beta Gsk C00003672 0 / 0
P55789 FAD-linked sulfhydryl oxidase ALR Enzyme C00002902 1 / 0
P03956 Interstitial collagenase M10A C00002648 0 / 1
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00002624 7 / 3
Q04206 Transcription factor p65 Transcription Factor C00006925 0 / 0
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00003740 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00006925 0 / 0
P11021 78 kDa glucose-regulated protein Unclassified protein C00006925 0 / 0
P22894 Neutrophil collagenase M10A C00002648 0 / 0
P00734 Prothrombin S1A C00003672 4 / 2
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00002902 2 / 2
P35218 Carbonic anhydrase 5A, mitochondrial Lyase C00000856 0 / 0
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00006925 5 / 3
P80404 4-aminobutyrate aminotransferase, mitochondrial Transferase C00000856 1 / 1
P12931 Proto-oncogene tyrosine-protein kinase Src Src C00006925 0 / 0
P35968 Vascular endothelial growth factor receptor 2 Vegfr C00006925 1 / 0
Q9Y2D0 Carbonic anhydrase 5B, mitochondrial Lyase C00000856 0 / 0
P08581 Hepatocyte growth factor receptor TK tyrosine-protein kinase MET subfamily C00006925 2 / 3
P10253 Lysosomal alpha-glucosidase Hydrolase C00002902 1 / 1
P04062 Glucosylceramidase Enzyme C00006925 6 / 4
P21802 Fibroblast growth factor receptor 2 TK tyrosine-protein kinase TLK subfamily C00006925 9 / 3
P08253 72 kDa type IV collagenase M10A C00002648 1 / 3
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00006925 3 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00006925 2 / 2
O15118 Niemann-Pick C1 protein Unclassified protein C00002902 1 / 1
Q01453 Peripheral myelin protein 22 Unclassified protein C00006925 5 / 2
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00006925 0 / 0
Q9HAW9 UDP-glucuronosyltransferase 1-8 Enzyme C00000856 0 / 0
Q13093 Platelet-activating factor acetylhydrolase Enzyme C00002776 3 / 0
P09884 DNA polymerase alpha catalytic subunit Transferase C00023774 0 / 0
P11362 Fibroblast growth factor receptor 1 Fgfr C00006925 4 / 5
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor C00006925 0 / 0
P05771 Protein kinase C beta type Alpha C00003740 0 / 0
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00006925 2 / 2
P21728 D(1A) dopamine receptor Dopamine receptor C00006925 0 / 0
P09917 Arachidonate 5-lipoxygenase Oxidoreductase C00002648 0 / 0
P14618 Pyruvate kinase PKM Enzyme C00006925 0 / 0
O60218 Aldo-keto reductase family 1 member B10 Enzyme C00019065 0 / 0
Q6W5P4 Neuropeptide S receptor Neuropeptide receptor C00006925 1 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00006925 0 / 0
P49798 Regulator of G-protein signaling 4 Unclassified protein C00003672 2 / 0
Q99549 M-phase phosphoprotein 8 Unclassified protein C00006925 0 / 0
P19224 UDP-glucuronosyltransferase 1-6 Enzyme C00000856 0 / 0
Q9HAW8 UDP-glucuronosyltransferase 1-10 Enzyme C00000856 0 / 0
P10721 Mast/stem cell growth factor receptor Kit Pdgfr C00006925 4 / 3
P05412 Transcription factor AP-1 Transcription Factor C00006925 0 / 0
P07451 Carbonic anhydrase 3 Lyase C00000856 0 / 0
P17706 Tyrosine-protein phosphatase non-receptor type 2 Tyr C00019065 0 / 1
P08254 Stromelysin-1 M10A C00002648 1 / 0
P22748 Carbonic anhydrase 4 Lyase C00000856 1 / 1
P80365 Corticosteroid 11-beta-dehydrogenase isozyme 2 Enzyme C00003672 1 / 1
Q9UBT6 DNA polymerase kappa Enzyme C00006925 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002902 0 / 0
P40225 Thrombopoietin Unclassified protein C00006925 1 / 1
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00006925 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00003672 1 / 1
P04637 Cellular tumor antigen p53 Transcription Factor C00006925 7 / 37
P42345 Serine/threonine-protein kinase mTOR Enzyme C00006925 0 / 0
P00519 Tyrosine-protein kinase ABL1 Abl C00002902 1 / 2
P11274 Breakpoint cluster region protein Bcr C00002902 1 / 2
Q02880 DNA topoisomerase 2-beta Isomerase C00023774 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00002776 0 / 0
P51531 Probable global transcription activator SNF2L2 Unclassified protein C00006925 1 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme C00006925 0 / 0

70 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
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) C00000856 C00002648
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) C00002682 C00006925
54577 UGT1A7, UDPGT, UDPGT_1-7, UGT-1G, UGT1-07, UGT1.7, UGT1G UDP glucuronosyltransferase 1 family, polypeptide A7 (EC:2.4.1.17) C00002682 C00006925
54575 UGT1A10, UDPGT, UGT-1J, UGT1-10, UGT1.10, UGT1J UDP glucuronosyltransferase 1 family, polypeptide A10 (EC:2.4.1.17) C00002682 C00006925
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00002902 C00006925
598 BCL2L1, BCL-XL/S, BCL2L, BCLX, BCLXL, BCLXS, Bcl-X, PPP1R52, bcl-xL, bcl-xS BCL2-like 1 C00002902 C00006925
4792 NFKBIA, IKBA, MAD-3, NFKBI nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha C00002902 C00006925
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00002902 C00006925
4609 MYC, MRTL, MYCC, bHLHe39, c-Myc v-myc avian myelocytomatosis viral oncogene homolog C00002902
329 BIRC2, API1, HIAP2, Hiap-2, MIHB, RNF48, c-IAP1, cIAP1 baculoviral IAP repeat containing 2 C00006925
3952 LEP, LEPD, OB, OBS leptin C00000856
6513 SLC2A1, DYT17, DYT18, DYT9, EIG12, GLUT, GLUT1, GLUT1DS, HTLVR, PED solute carrier family 2 (facilitated glucose transporter), member 1 C00006925
54658 UGT1A1, BILIQTL1, GNT1, HUG-BR1, UDPGT, UDPGT_1-1, UGT1, UGT1A UDP glucuronosyltransferase 1 family, polypeptide A1 (EC:2.4.1.17) C00006925
1499 CTNNB1, CTNNB, MRD19, armadillo catenin (cadherin-associated protein), beta 1, 88kDa C00003749
2539 G6PD, G6PD1 glucose-6-phosphate dehydrogenase (EC:1.1.1.49) C00002648
5728 PTEN, 10q23del, BZS, CWS1, DEC, GLM2, MHAM, MMAC1, PTEN1, TEP1 phosphatase and tensin homolog (EC:3.1.3.67 3.1.3.16 3.1.3.48) C00003749
54600 UGT1A9, HLUGP4, LUGP4, UDPGT, UDPGT_1-9, UGT-1I, UGT1-09, UGT1-9, UGT1.9, UGT1AI, UGT1I UDP glucuronosyltransferase 1 family, polypeptide A9 (EC:2.4.1.17) C00006925
207 AKT1, AKT, CWS6, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA v-akt murine thymoma viral oncogene homolog 1 (EC:2.7.11.1) C00002902
23600 AMACR, AMACRD, CBAS4, RACE, RM alpha-methylacyl-CoA racemase (EC:5.1.99.4) C00002902
1386 ATF2, CRE-BP1, CREB2, HB16, TREB7 activating transcription factor 2 (EC:2.3.1.48) C00002902
578 BAK1, BAK, BAK-LIKE, BCL2L7, CDN1 BCL2-antagonist/killer 1 C00002902
581 BAX, BCL2L4 BCL2-associated X protein C00002902
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00002902
842 CASP9, APAF-3, APAF3, ICE-LAP6, MCH6, PPP1R56 caspase 9, apoptosis-related cysteine peptidase (EC:3.4.22.62) C00002902
595 CCND1, BCL1, D11S287E, PRAD1, U21B31 cyclin D1 C00002902
1026 CDKN1A, CAP20, CDKN1, CIP1, MDA-6, P21, SDI1, WAF1, p21CIP1 cyclin-dependent kinase inhibitor 1A (p21, Cip1) C00002902
1027 CDKN1B, CDKN4, KIP1, MEN1B, MEN4, P27KIP1 cyclin-dependent kinase inhibitor 1B (p27, Kip1) C00002902
2921 CXCL3, CINC-2b, GRO3, GROg, MIP-2b, MIP2B, SCYB3 chemokine (C-X-C motif) ligand 3 C00002902
54205 CYCS, CYC, HCS, THC4 cytochrome c, somatic C00002902
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00002902
1649 DDIT3, CEBPZ, CHOP, CHOP-10, CHOP10, GADD153 DNA-damage-inducible transcript 3 C00002902
56616 DIABLO, DFNA64, SMAC diablo, IAP-binding mitochondrial protein C00002902
1950 EGF, HOMG4, URG epidermal growth factor C00002902
1956 EGFR, ERBB, ERBB1, HER1, PIG61, mENA epidermal growth factor receptor (EC:2.7.10.1) C00002902
2002 ELK1 ELK1, member of ETS oncogene family C00002902
2523 FUT1, H, HH, HSC fucosyltransferase 1 (galactoside 2-alpha-L-fucosyltransferase, H blood group) (EC:2.4.1.69) C00002902
9518 GDF15, GDF-15, MIC-1, MIC1, NAG-1, PDF, PLAB, PTGFB growth differentiation factor 15 C00002902
3162 HMOX1, HMOX1D, HO-1, HSP32, bK286B10 heme oxygenase (decycling) 1 (EC:1.14.99.3) C00002902
4670 HNRNPM, CEAR, HNRNPM4, HNRPM, HNRPM4, HTGR1, NAGR1, hnRNP_M heterogeneous nuclear ribonucleoprotein M C00002902
3313 HSPA9, CSA, GRP-75, GRP75, HSPA9B, MOT, MOT2, MTHSP75, PBP74 heat shock 70kDa protein 9 (mortalin) C00002902
3458 IFNG, IFG, IFI interferon, gamma C00002902
3553 IL1B, IL-1, IL1-BETA, IL1F2 interleukin 1, beta C00002902
3696 ITGB8 integrin, beta 8 C00002902
3717 JAK2, JTK10, THCYT3 Janus kinase 2 (EC:2.7.10.2) C00002902
3949 LDLR, FH, FHC, LDLCQ2 low density lipoprotein receptor C00002902
5594 MAPK1, ERK, ERK2, ERT1, MAPK2, P42MAPK, PRKM1, PRKM2, p38, p40, p41, p41mapk mitogen-activated protein kinase 1 (EC:2.7.11.24) C00002902
1432 MAPK14, CSBP, CSBP1, CSBP2, CSPB1, EXIP, Mxi2, PRKM14, PRKM15, RK, SAPK2A, p38, p38ALPHA mitogen-activated protein kinase 14 (EC:2.7.11.24) C00002902
5595 MAPK3, ERK-1, ERK1, ERT2, HS44KDAP, HUMKER1A, P44ERK1, P44MAPK, PRKM3, p44-ERK1, p44-MAPK mitogen-activated protein kinase 3 (EC:2.7.11.24) C00002902
5599 MAPK8, JNK, JNK-46, JNK1, JNK1A2, JNK21B1/2, PRKM8, SAPK1, SAPK1c mitogen-activated protein kinase 8 (EC:2.7.11.24) C00002902
5601 MAPK9, JNK-55, JNK2, JNK2A, JNK2ALPHA, JNK2B, JNK2BETA, PRKM9, SAPK, SAPK1a, p54a, p54aSAPK mitogen-activated protein kinase 9 (EC:2.7.11.24) C00002902
4170 MCL1, BCL2L3, EAT, MCL1-ES, MCL1L, MCL1S, Mcl-1, TM, bcl2-L-3, mcl1/EAT myeloid cell leukemia sequence 1 (BCL2-related) C00002902
4318 MMP9, CLG4B, GELB, MANDP2, MMP-9 matrix metallopeptidase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase) (EC:3.4.24.35) C00002902
330 BIRC3, AIP1, API2, CIAP2, HAIP1, HIAP1, MALT2, MIHC, RNF49, c-IAP2 baculoviral IAP repeat containing 3 C00006925
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 C00002902
4843 NOS2, HEP-NOS, INOS, NOS, NOS2A nitric oxide synthase 2, inducible (EC:1.14.13.39) C00002902
8856 NR1I2, BXR, ONR1, PAR, PAR1, PAR2, PARq, PRR, PXR, SAR, SXR nuclear receptor subfamily 1, group I, member 2 C00002902
9970 NR1I3, CAR, CAR1, MB67 nuclear receptor subfamily 1, group I, member 3 C00002902
142 PARP1, ADPRT, ADPRT_1, ADPRT1, ARTD1, PARP, PARP-1, PPOL, pADPRT-1 poly (ADP-ribose) polymerase 1 (EC:2.4.2.30) C00002902
5743 PTGS2, COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2, hCox-2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase) (EC:1.14.99.1) C00002902
6301 SARS, SERRS, SERS seryl-tRNA synthetase (EC:6.1.1.11) C00002902
6648 SOD2, IPOB, MNSOD, MVCD6 superoxide dismutase 2, mitochondrial (EC:1.15.1.1) C00002902
6667 SP1 Sp1 transcription factor C00002902
6774 STAT3, APRF, HIES signal transducer and activator of transcription 3 (acute-phase response factor) C00002902
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00002902
7157 TP53, BCC7, LFS1, P53, TRP53 tumor protein p53 C00002902
9189 ZBED1, ALTE, DREF, TRAMP, hDREF zinc finger, BED-type containing 1 C00002902
118738 ZNF488 zinc finger protein 488 C00002902
10599 SLCO1B1, HBLRR, LST-1, LST1, OATP-C, OATP1B1, OATP2, OATPC, SLC21A6 solute carrier organic anion transporter family, member 1B1 C00023774
4846 NOS3, ECNOS, eNOS nitric oxide synthase 3 (endothelial cell) (EC:1.14.13.39) C00002682
54659 UGT1A3, UDPGT, UDPGT_1-3, UGT-1C, UGT1-03, UGT1.3, UGT1C UDP glucuronosyltransferase 1 family, polypeptide A3 (EC:2.4.1.17) C00002682

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (135)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#103470 Albinism, ocular, with sensorineural deafness P14679
#203100 Albinism, oculocutaneous, type ia; oca1a P14679
#606952 Albinism, oculocutaneous, type ib; oca1b P14679
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#207410 Antley-bixler syndrome without genital anomalies or disordered steroidogenesis; abs2 P21802
#101200 Apert syndrome P21802
#218030 Apparent mineralocorticoid excess; ame P80365
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#600807 Asthma, susceptibility to Q13093
#608584 Asthma-related traits, susceptibility to, 2 Q6W5P4
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#123790 Beare-stevenson cutis gyrata syndrome; bstvs P21802
#614592 Bent bone dysplasia syndrome; bbds P21802
#210900 Bloom syndrome; blm P54132
%606641 Body mass index; bmi P37231
#114480 Breast cancer P38398
#604370 Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 P38398
#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
#123500 Crouzon syndrome P21802
#127750 Dementia, lewy body; dlb P37840
#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
#615363 Estrogen resistance; estrr P03372
#600274 Frontotemporal dementia; ftd P10636
#613163 Gaba-transaminase deficiency P80404
#606764 Gastrointestinal stromal tumor; gist P10721
#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
#137800 Glioma susceptibility 1; glm1 O75874
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
#602089 Hemangioma, capillary infantile P35968
#114550 Hepatocellular carcinoma P08581
#143100 Huntington disease; hd P42858
#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
#147950 Hypogonadotropic hypogonadism 2 with or without anosmia; hh2 P11362
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#147050 Ige responsiveness, atopic; iger Q13093
#612244 Inflammatory bowel disease 13; ibd13 P08183
#603932 Intervertebral disc disease; idd P14780
#123150 Jackson-weiss syndrome; jws P21802
#149730 Lacrimoauriculodentodigital syndrome; ladd P21802
#601626 Leukemia, acute myeloid; aml P10721
#608232 Leukemia, chronic myeloid; cml P00519
P11274
#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
P04637
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#174800 Mccune-albright syndrome; mas P63092
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#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
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#613076 Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay P55789
#162500 Neuropathy, hereditary, with liability to pressure palsies; hnpp Q01453
#601358 Nicolaides-baraitser syndrome; ncbrs P51531
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#257220 Niemann-pick disease, type c1; npc1 O15118
#601665 Obesity P37231
#166350 Osseous heteroplasia, progressive; poh P63092
#166250 Osteoglophonic dysplasia; ogd P11362
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#167000 Ovarian cancer 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 P04062
P37840
#260540 Parkinson-dementia syndrome P10636
#101600 Pfeiffer syndrome P11362
P21802
#172700 Pick disease of brain P10636
#172800 Piebald trait; pbt P10721
#102200 Pituitary adenoma, growth hormone-secreting P63092
#614278 Platelet-activating factor acetylhydrolase deficiency; pafad Q13093
#614390 Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 P00734
#613679 Prothrombin deficiency, congenital P00734
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#605074 Renal cell carcinoma, papillary, 1; rccp1 P08581
#275210 Restrictive dermopathy, lethal P02545
#600852 Retinitis pigmentosa 17; rp17 P22748
#609579 Scaphocephaly, maxillary retrusion, and mental retardation P21802
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#609620 Short qt syndrome 1; sqt1 Q12809
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679
#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
#601367 Stroke, ischemic P00734
#271980 Succinic semialdehyde dehydrogenase deficiency; ssadhd P51649
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#273300 Testicular germ cell tumor; tgct P10721
#610460 Thiopurine s-methyltransferase deficiency P51580
#187950 Thrombocythemia 1; thcyt1 P40225
#188050 Thrombophilia due to thrombin defect; thph1 P00734
#188570 Thyroid hormone resistance, generalized, autosomal dominant; grth P10828
#274300 Thyroid hormone resistance, generalized, autosomal recessive; grth P10828
#145650 Thyroid hormone resistance, selective pituitary; prth P10828
#190440 Trigonocephaly 1; trigno1 P11362
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (116)

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)
P08581 (related)
Q16790 (marker)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) P00519 (related)
P00519 (marker)
P11274 (related)
P11274 (marker)
Q03164 (related)
Q03164 (marker)
H00004 Chronic myeloid leukemia (CML) P00519 (related)
P00519 (marker)
P04637 (related)
P11274 (related)
P11274 (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)
P04637 (related)
P08581 (related)
P21802 (related)
H00022 Bladder cancer P00533 (related)
P04637 (related)
H00028 Choriocarcinoma P00533 (related)
P03956 (related)
P04637 (related)
P08253 (related)
H00030 Cervical cancer P00533 (related)
H00042 Glioma P00533 (related)
P00533 (marker)
P04637 (related)
P04637 (marker)
H00055 Laryngeal cancer P00533 (related)
P00533 (marker)
P04637 (related)
P04637 (marker)
H00223 Inherited thrombophilia P00734 (related)
H01254 Congenital prothrombin deficiency P00734 (related)
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)
P04637 (related)
H00066 Lewy body dementia (LBD) P04062 (related)
P37840 (related)
H00126 Gaucher disease P04062 (related)
H00426 Defects in the degradation of ganglioside P04062 (related)
H00810 Progressive myoclonic epilepsy (PME) P04062 (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)
H00019 Pancreatic cancer P04637 (related)
P04637 (marker)
H00020 Colorectal cancer P04637 (related)
P04637 (marker)
H00025 Penile cancer P04637 (related)
P04637 (marker)
P08253 (related)
P14780 (related)
P35354 (related)
H00027 Ovarian cancer P04637 (related)
P38398 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
P38398 (related)
H00032 Thyroid cancer P04637 (related)
P37231 (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)
H00046 Cholangiocarcinoma P04637 (related)
P08581 (related)
P35354 (related)
H00047 Gallbladder cancer P04637 (related)
H00048 Hepatocellular carcinoma P04637 (related)
H00881 Li-Fraumeni syndrome P04637 (related)
H01007 Choroid plexus papilloma P04637 (related)
H00472 Torg-Winchester syndrome P08253 (related)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00003 Acute myeloid leukemia (AML) P10721 (related)
P10721 (marker)
H00170 Piebaldism P10721 (related)
H00023 Testicular cancer P10721 (marker)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00255 Hypogonadotropic hypogonadism P11362 (related)
H00443 Osteoglophonic dysplasia (OD) P11362 (related)
H00458 Craniosynostosis P11362 (related)
P21802 (related)
H00516 Isolated orofacial clefts P11362 (related)
H01207 Trigonocephaly P11362 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P11511 (related)
H00794 Aromatase excess syndrome P11511 (related)
H01205 Coumarin resistance P11712 (related)
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00479 Metaphyseal dysplasias P14780 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
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)
H00408 Type I diabetes mellitus P17706 (related)
H00642 Lacrimo-auriculo-dento-digital syndrome (LADD) P21802 (related)
H00527 Retinitis pigmentosa (RP) P22748 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00057 Parkinson's disease (PD) P37840 (related)
H00227 Congenital amegakaryocytic thrombocytopenia (CAMT) P40225 (marker)
H00059 Huntington's disease (HD) P42858 (related)
H00964 Thiopurine S-methyltransferase deficiency (TPMT deficiency) P51580 (related)
H00835 Succinic semialdehyde dehydrogenase (SSADH) deficiency P51649 (related)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00259 Apparent mineralocorticoid excess syndrome P80365 (related)
H01257 GABA-transaminase deficiency P80404 (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)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (related)
H00480 Non-syndromic X-linked mental retardation Q99714 (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

33 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D003110 Colonic Neoplasms C00003740
C00002902
D007249 Inflammation C00003738
C00002902
D006528 Carcinoma, Hepatocellular C00003749
C00002902
D012878 Skin Neoplasms C00003749
C00002902
D009422 Nervous System Diseases C00006925
D009374 Neoplasms, Experimental C00003749
D009202 Cardiomyopathies C00003749
D014947 Wounds and Injuries C00003749
D006461 Hemolysis C00002648
D005157 Facial Pain C00003738
D006930 Hyperalgesia C00003738
D064420 Drug-Related Side Effects and Adverse Reactions C00003740
D010146 Pain C00003738
D012220 Rhinitis C00000856
D001927 Brain Diseases C00006925
D009120 Muscle Cramp C00006925
D006937 Hypercholesterolemia C00003749
D000647 Amnesia C00002776
D000860 Anoxia C00002776
D001930 Brain Injuries C00002776
D056486 Drug-Induced Liver Injury C00002776
D004487 Edema C00002776
D058739 Aberrant Crypt Foci C00002902
D000236 Adenoma C00002902
D001943 Breast Neoplasms C00002902
D002471 Cell Transformation, Neoplastic C00002902
D015179 Colorectal Neoplasms C00002902
D015464 Leukemia, Myelogenous, Chronic, BCR-ABL Positive C00002902
D009361 Neoplasm Invasiveness C00002902
D009362 Neoplasm Metastasis C00002902
D012516 Osteosarcoma C00002902
D010190 Pancreatic Neoplasms C00002902
D010212 Papilloma C00002902