Species

KNApSAcK Entry

Organism name Salvia miltiorrhiza
Genus Salvia
Family Labiatae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Salvia miltiorrhiza
Linked NCBI taxonomy ID 226208
Linked level species

Family

Family in NCBI taxonomy Lamiaceae
ID 4136

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Natural Activity

List (38)

Species Activity
Salvia miltiorrhiza Bunge Alterative
Salvia miltiorrhiza Bunge Antiaggregant
Salvia miltiorrhiza Bunge Antiaging
Salvia miltiorrhiza Bunge Antiallergic
Salvia miltiorrhiza Bunge Antiandrogenic
Salvia miltiorrhiza Bunge Antianginal
Salvia miltiorrhiza Bunge Antiarthritic
Salvia miltiorrhiza Bunge Antibacterial
Salvia miltiorrhiza Bunge Anticarcinomic
Salvia miltiorrhiza Bunge Antihypoxic
Salvia miltiorrhiza Bunge Antiinflammatory
Salvia miltiorrhiza Bunge Antimutagenic
Salvia miltiorrhiza Bunge Antioxidant
Salvia miltiorrhiza Bunge Antipyretic
Salvia miltiorrhiza Bunge Antiseptic
Salvia miltiorrhiza Bunge Antispasmodic
Salvia miltiorrhiza Bunge Antithrombic
Salvia miltiorrhiza Bunge Astringent
Salvia miltiorrhiza Bunge Bitter
Salvia miltiorrhiza Bunge Calcium Antagonist
Salvia miltiorrhiza Bunge Cardioprotective
Salvia miltiorrhiza Bunge Cardiotonic
Salvia miltiorrhiza Bunge Circulotonic
Salvia miltiorrhiza Bunge Fibrinolytic
Salvia miltiorrhiza Bunge Fungicide
Salvia miltiorrhiza Bunge Hepatoprotective
Salvia miltiorrhiza Bunge Hepatoregenerative
Salvia miltiorrhiza Bunge Hyocholesterolemic
Salvia miltiorrhiza Bunge Hypotensive
Salvia miltiorrhiza Bunge Lipolytic
Salvia miltiorrhiza Bunge Negative Inotropic
Salvia miltiorrhiza Bunge Nephroprotective
Salvia miltiorrhiza Bunge Sedative
Salvia miltiorrhiza Bunge Swelling
Salvia miltiorrhiza Bunge Tonic
Salvia miltiorrhiza Bunge Tranquilizer
Salvia miltiorrhiza Bunge Vasodilator
Salvia miltiorrhiza Bunge Vulnerary

Metabolite list (23)

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
C00036584 External link 512 5,3'-Dihydroxy-7-4'-dimethoxyflavanone
No. 25 No. 14
C00002772 External link 512 Salvianolic acid A
CHEMBL457077
C066201
5 / 5 / 7 0 / 3 No. 494
C00037773 External link 512 Salvianolic acid C
No. 494
C00002770 External link 512 Rosmarinic acid
CHEMBL66966
CHEMBL324842
CHEMBL1315100
CHEMBL2111558
48 / 35 / 38 No. 749
C00037774 External link 512 Salvianolic acid D
No. 749
C00037499 External link 512 Methyl rosmarinate
/ (+)-Methyl rosmarinate
CHEMBL241405
CHEMBL1765650
6 / 5 / 4 No. 749
C00037775 External link 512 Salvianolic acid E
No. 1276
C00002752 External link 512 Isoferulic acid
CHEMBL233295
C008180
5 / 9 / 6 0 / 1 No. 1366 No. 6
C00030792 External link 512 Montbretol
/ 6,12-Dihydroxyabieta-5,8,11,13-tetraen-7-one
CHEMBL469670
No. 1418
C00037776 External link 512 Salvianolic acid F
CHEMBL464884
No. 1951
C00031719 External link 512 Danshenspiroketallactone
No. 2567
C00031402 External link 512 Tanshinone II
/ Tanshinone IIA
CHEMBL187266
44 / 56 / 79 No. 3852
C00042764 External link 512 Neosalvianen
CHEMBL520209
No. 4117
C00042927 External link 512 Salvianan
No. 4117
C00042928 External link 512 Salvianen
CHEMBL450365
No. 4117
C00037059 External link 512 Dimethyl lithospermate
CHEMBL2048505
6 / 5 / 4 No. 4991
C00046227 External link 512 Oleoyl danshenxinkun A
/ (-)-Oleoyl danshenxinkun A
CHEMBL473262
No. 5394
C00046228 External link 512 Oleoyl neocryptotanshinone
CHEMBL445779
No. 5394
C00031401 External link 512 Tanshinone I
/ Tanshinone A
CHEMBL363535
C021751
26 / 35 / 57 84 / 6 No. 5517
C00037777 External link 512 Salvianolic acid G
/ (-)-Salvianolic acid G
No. 6009
C00042926 External link 512 Salviadione
CHEMBL449895
No. 7215
C00037545 External link 512 Neocryptotanshinone II
No. 8610
C00042146 External link 512 5-(Methoxymethyl)-1H-pyrrole-2-carbaldehyde
No. 8926

Human Protein / Gene in interactions

81 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00002752 C00002770 C00031401 C00031402 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00002752 C00002770 C00031401 C00031402 0 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00002770 C00031401 C00031402 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00002752 C00031401 C00031402 7 / 3
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00002770 C00031401 C00031402 1 / 1
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00002770 C00031401 C00031402 0 / 0
P03956 Interstitial collagenase M10A C00002770 C00037059 C00037499 0 / 1
Q9Y253 DNA polymerase eta Enzyme C00002770 C00031401 C00031402 1 / 1
P39748 Flap endonuclease 1 Enzyme C00002770 C00031401 C00031402 0 / 0
P06746 DNA polymerase beta Enzyme C00002770 C00031401 C00031402 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00002770 C00031401 C00031402 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00002770 C00031401 C00031402 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00002770 C00031401 C00031402 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00002770 C00031401 C00031402 4 / 3
P54132 Bloom syndrome protein Enzyme C00002770 C00031401 1 / 2
O14746 Telomerase reverse transcriptase Enzyme C00031401 C00031402 5 / 5
P23141 Liver carboxylesterase 1 Enzyme C00031401 C00031402 0 / 0
P08254 Stromelysin-1 M10A C00037059 C00037499 1 / 0
P06239 Tyrosine-protein kinase Lck Src C00002770 C00002772 0 / 1
P39900 Macrophage metalloelastase M10A C00037059 C00037499 0 / 0
O00748 Cocaine esterase Enzyme C00031401 C00031402 0 / 0
P14780 Matrix metalloproteinase-9 M10A C00037059 C00037499 2 / 2
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00002770 C00031402 1 / 0
P11473 Vitamin D3 receptor NR1I1 C00031401 C00031402 2 / 3
Q12794 Hyaluronidase-1 Enzyme C00002752 C00002770 1 / 2
P22303 Acetylcholinesterase Hydrolase C00031401 C00031402 1 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002770 C00031402 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00002770 C00031402 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00002770 C00031402 0 / 0
O75496 Geminin Unclassified protein C00031401 C00031402 0 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002770 C00031402 2 / 2
P15121 Aldose reductase Enzyme C00002770 C00031402 0 / 0
P40763 Signal transducer and activator of transcription 3 Transcription Factor C00002770 C00002772 1 / 2
P42224 Signal transducer and activator of transcription 1-alpha/beta Unclassified protein C00002770 C00002772 3 / 3
P04637 Cellular tumor antigen p53 Transcription Factor C00031401 C00031402 7 / 37
Q13951 Core-binding factor subunit beta Unclassified protein C00002770 C00031402 0 / 1
P51692 Signal transducer and activator of transcription 5B Unclassified protein C00002770 C00002772 1 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00002770 C00031402 1 / 4
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00002770 C00031402 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00002770 C00031402 3 / 3
P08253 72 kDa type IV collagenase M10A C00037059 C00037499 1 / 3
P12931 Proto-oncogene tyrosine-protein kinase Src Src C00002770 C00002772 0 / 0
P45452 Collagenase 3 M10A C00037059 C00037499 1 / 1
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00031402 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00031402 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00002770 0 / 0
P06401 Progesterone receptor NR3C3 C00031402 0 / 1
P04150 Glucocorticoid receptor NR3C1 C00031402 0 / 1
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00031402 0 / 0
P38398 Breast cancer type 1 susceptibility protein Enzyme C00031401 4 / 2
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00031402 2 / 0
P03372 Estrogen receptor NR3A1 C00002752 1 / 1
P00352 Retinal dehydrogenase 1 Enzyme C00031402 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00002770 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002770 0 / 1
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00002770 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00002770 0 / 1
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00002770 0 / 0
P06241 Tyrosine-protein kinase Fyn Src C00002770 0 / 0
O14727 Apoptotic protease-activating factor 1 Unclassified protein C00031402 0 / 0
P18054 Arachidonate 12-lipoxygenase, 12S-type Enzyme C00031402 2 / 0
P10275 Androgen receptor NR3C4 C00031402 3 / 4
P10828 Thyroid hormone receptor beta NR1A2 C00002770 3 / 1
P02545 Prelamin-A/C Unclassified protein C00031402 11 / 10
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00002770 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00031401 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00002770 1 / 1
P04062 Glucosylceramidase Enzyme C00002770 6 / 4
Q13093 Platelet-activating factor acetylhydrolase Enzyme C00002770 3 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00002770 0 / 3
P14618 Pyruvate kinase PKM Enzyme C00002770 0 / 0
P49798 Regulator of G-protein signaling 4 Unclassified protein C00031402 2 / 0
Q99700 Ataxin-2 Unclassified protein C00031401 1 / 1
O00255 Menin Unclassified protein C00031402 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00031402 1 / 2
Q07820 Induced myeloid leukemia cell differentiation protein Mcl-1 Other cytosolic protein C00002770 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00002770 1 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00002770 0 / 0
P01215 Glycoprotein hormones alpha chain Unclassified protein C00031401 0 / 3
Q9H0H5 Rac GTPase-activating protein 1 Unclassified protein C00002770 0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00031401 1 / 1

84 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
37 ACADVL, ACAD6, LCACD, VLCAD acyl-CoA dehydrogenase, very long chain (EC:1.3.8.9) C00031401
2180 ACSL1, ACS1, FACL1, FACL2, LACS, LACS1, LACS2 acyl-CoA synthetase long-chain family member 1 (EC:6.2.1.3) C00031401
196 AHR, bHLHe76 aryl hydrocarbon receptor C00031401
220 ALDH1A3, ALDH1A6, ALDH6, MCOP8, RALDH3 aldehyde dehydrogenase 1 family, member A3 (EC:1.2.1.5) C00031401
224 ALDH3A2, ALDH10, FALDH, SLS aldehyde dehydrogenase 3 family, member A2 (EC:1.2.1.3) C00031401
341 APOC1 apolipoprotein C-I C00031401
55937 APOM, G3a, HSPC336, NG20, apo-M apolipoprotein M C00031401
440 ASNS, TS11 asparagine synthetase (glutamine-hydrolyzing) (EC:6.3.5.4) C00031401
445 ASS1, ASS, CTLN1 argininosuccinate synthase 1 (EC:6.3.4.5) C00031401
533 ATP6V0B, ATP6F, HATPL, VMA16 ATPase, H+ transporting, lysosomal 21kDa, V0 subunit b (EC:3.6.3.14) C00031401
529 ATP6V1E1, ATP6E, ATP6E2, ATP6V1E, P31, Vma4 ATPase, H+ transporting, lysosomal 31kDa, V1 subunit E1 (EC:3.6.3.14) C00031401
581 BAX, BCL2L4 BCL2-associated X protein C00031401
594 BCKDHB, E1B, dJ279A18.1 branched chain keto acid dehydrogenase E1, beta polypeptide (EC:1.2.4.4) C00031401
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00031401
330 BIRC3, AIP1, API2, CIAP2, HAIP1, HIAP1, MALT2, MIHC, RNF49, c-IAP2 baculoviral IAP repeat containing 3 C00031401
332 BIRC5, API4, EPR-1 baculoviral IAP repeat containing 5 C00031401
10241 CALCOCO2, NDP52 calcium binding and coiled-coil domain 2 C00031401
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00031401
945 CD33, SIGLEC-3, SIGLEC3, p67 CD33 molecule C00031401
1026 CDKN1A, CAP20, CDKN1, CIP1, MDA-6, P21, SDI1, WAF1, p21CIP1 cyclin-dependent kinase inhibitor 1A (p21, Cip1) C00031401
4680 CEACAM6, CD66c, CEAL, NCA carcinoembryonic antigen-related cell adhesion molecule 6 (non-specific cross reacting antigen) C00031401
1191 CLU, APO-J, APOJ, CLI, CLU1, CLU2, KUB1, NA1/NA2, SGP-2, SGP2, SP-40, TRPM-2, TRPM2 clusterin C00031401
1291 COL6A1, OPLL collagen, type VI, alpha 1 C00031401
1474 CST6 cystatin E/M C00031401
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00031401
1544 CYP1A2, CP12, P3-450, P450(PA) cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) C00031401
25642 C00031401
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) C00031401
1633 DCK deoxycytidine kinase (EC:2.7.1.74) C00031401
8446 DUSP11, PIR1 dual specificity phosphatase 11 (RNA/RNP complex 1-interacting) (EC:3.1.3.16 3.1.3.48) C00031401
1847 DUSP5, DUSP, HVH3 dual specificity phosphatase 5 (EC:3.1.3.16 3.1.3.48) C00031401
8798 DYRK4 dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 4 (EC:2.7.12.1) C00031401
8507 ENC1, CCL28, ENC-1, KLHL35, KLHL37, NRPB, PIG10, TP53I10 ectodermal-neural cortex 1 (with BTB domain) C00031401
2067 ERCC1, COFS4, RAD10, UV20 excision repair cross-complementing rodent repair deficiency, complementation group 1 (includes overlapping antisense sequence) C00031401
2114 ETS2, ETS2IT1 v-ets avian erythroblastosis virus E26 oncogene homolog 2 C00031401
2150 F2RL1, GPR11, PAR2 coagulation factor II (thrombin) receptor-like 1 C00031401
80308 FLAD1, FAD1, FADS, RP11-307C12.7 flavin adenine dinucleotide synthetase 1 (EC:2.7.7.2) C00031401
2353 FOS, AP-1, C-FOS, p55 FBJ murine osteosarcoma viral oncogene homolog C00031401
2629 GBA, GBA1, GCB, GLUC glucosidase, beta, acid (EC:3.2.1.45) C00031401
2670 GFAP glial fibrillary acidic protein C00031401
2886 GRB7 growth factor receptor-bound protein 7 C00031401
2950 GSTP1, DFN7, FAEES3, GST3, GSTP, PI glutathione S-transferase pi 1 (EC:2.5.1.18) C00031401
8841 HDAC3, HD3, RPD3, RPD3-2 histone deacetylase 3 (EC:3.5.1.98) C00031401
3398 ID2, GIG8, ID2A, ID2H, bHLHb26 inhibitor of DNA binding 2, dominant negative helix-loop-helix protein C00031401
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00031401
3636 INPPL1, OPSMD, SHIP2 inositol polyphosphate phosphatase-like 1 (EC:3.1.3.86) C00031401
3669 ISG20, CD25, HEM45 interferon stimulated exonuclease gene 20kDa (EC:3.1.13.1) C00031401
3655 ITGA6, CD49f, ITGA6B, VLA-6 integrin, alpha 6 C00031401
3684 ITGAM, CD11B, CR3A, MAC-1, MAC1A, MO1A, SLEB6 integrin, alpha M (complement component 3 receptor 3 subunit) C00031401
4035 LRP1, A2MR, APOER, APR, CD91, IGFBP3R, LRP, LRP1A, TGFBR5 low density lipoprotein receptor-related protein 1 C00031401
4041 LRP5, BMND1, EVR1, EVR4, HBM, LR3, LRP7, OPPG, OPS, OPTA1, VBCH2 low density lipoprotein receptor-related protein 5 C00031401
7804 LRP8, APOER2, HSZ75190, LRP-8, MCI1 low density lipoprotein receptor-related protein 8, apolipoprotein e receptor C00031401
4129 MAOB monoamine oxidase B (EC:1.4.3.4) C00031401
4214 MAP3K1, MAPKKK1, MEKK, MEKK_1, MEKK1, SRXY6 mitogen-activated protein kinase kinase kinase 1, E3 ubiquitin protein ligase (EC:2.7.11.25) C00031401
4285 MIPEP, HMIP, MIP mitochondrial intermediate peptidase (EC:3.4.24.59) C00031401
4316 MMP7, MMP-7, MPSL1, PUMP-1 matrix metallopeptidase 7 (matrilysin, uterine) (EC:3.4.24.23) C00031401
4605 MYBL2, B-MYB, BMYB v-myb avian myeloblastosis viral oncogene homolog-like 2 C00031401
4609 MYC, MRTL, MYCC, bHLHe39, c-Myc v-myc avian myelocytomatosis viral oncogene homolog C00031401
4632 MYL1, MLC1F, MLC3F myosin, light chain 1, alkali; skeletal, fast C00031401
8260 NAA10, ARD1, ARD1A, ARD1P, DXS707, NATD, TE2 N(alpha)-acetyltransferase 10, NatA catalytic subunit (EC:2.3.1.88) C00031401
4708 NDUFB2, AGGG, CI-AGGG NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 2, 8kDa (EC:1.6.5.3 1.6.99.3) C00031401
4723 NDUFV1, CI-51K, CI51KD, UQOR1 NADH dehydrogenase (ubiquinone) flavoprotein 1, 51kDa (EC:1.6.5.3 1.6.99.3) C00031401
10763 NES nestin C00031401
4846 NOS3, ECNOS, eNOS nitric oxide synthase 3 (endothelial cell) (EC:1.14.13.39) C00031401
8856 NR1I2, BXR, ONR1, PAR, PAR1, PAR2, PARq, PRR, PXR, SAR, SXR nuclear receptor subfamily 1, group I, member 2 C00031401
9970 NR1I3, CAR, CAR1, MB67 nuclear receptor subfamily 1, group I, member 3 C00031401
2908 NR3C1, GCCR, GCR, GR, GRL nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor) C00031401
44039 C00031401
143 PARP4, ADPRTL1, ARTD4, PARP-4, PARPL, PH5P, VAULT3, VPARP, VWA5C, p193 poly (ADP-ribose) polymerase family, member 4 (EC:2.4.2.30) C00031401
9159 PCSK7, LPC, PC7, PC8, SPC7 proprotein convertase subtilisin/kexin type 7 (EC:3.4.21.-) C00031401
5352 PLOD2, LH2, TLH procollagen-lysine, 2-oxoglutarate 5-dioxygenase 2 (EC:1.14.11.4) C00031401
24148 PRPF6, ANT-1, ANT1, C20orf14, Prp6, SNRNP102, TOM, U5-102K, hPrp6 pre-mRNA processing factor 6 C00031401
5693 PSMB5, LMPX, MB1, X proteasome (prosome, macropain) subunit, beta type, 5 (EC:3.4.25.1) C00031401
5708 PSMD2, P97, RPN1, S2, TRAP2 proteasome (prosome, macropain) 26S subunit, non-ATPase, 2 C00031401
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) C00031401
5796 PTPRK, R-PTP-kappa protein tyrosine phosphatase, receptor type, K (EC:3.1.3.48) C00031401
389 RHOC, ARH9, ARHC, H9, RHOH9 ras homolog family member C C00031401
6668 SP2 Sp2 transcription factor C00031401
352933 C00031401
7016 TESK1 testis-specific kinase 1 (EC:2.7.12.1) C00031401
7023 TFAP4, AP-4, bHLHc41 transcription factor AP-4 (activating enhancer binding protein 4) C00031401
7083 TK1, TK2 thymidine kinase 1, soluble (EC:2.7.1.21) C00031401
7157 TP53, BCC7, LFS1, P53, TRP53 tumor protein p53 C00031401
10406 WFDC2, EDDM4, HE4, WAP5, dJ461P17.6 WAP four-disulfide core domain 2 C00031401

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (90)

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
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#609135 Aplastic anemia O14746
#600807 Asthma, susceptibility to Q13093
#209950 Atypical mycobacteriosis, familial P42224
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#210900 Bloom syndrome; blm P54132
#114480 Breast cancer P38398
#604370 Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 P38398
#614162 Candidiasis, familial, 7; candf7 P42224
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#114500 Colorectal cancer; crc P18054
P84022
#614466 Coronary heart disease, susceptibility to, 6; chds6 P08254
#119900 Digital clubbing, isolated congenital P15428
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#613989 Dyskeratosis congenita, autosomal dominant, 2; dkca2 O14746
#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
#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
#232300 Glycogen storage disease ii P10253
#245590 Growth hormone insensitivity with immunodeficiency P51692
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#147060 Hyper-ige recurrent infection syndrome, autosomal dominant P40763
#145000 Hyperparathyroidism 1; hrpt1 O00255
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#147050 Ige responsiveness, atopic; iger Q13093
#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
#211980 Lung cancer P04637
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#174800 Mccune-albright syndrome; mas P63092
#615134 Melanoma, cutaneous malignant, susceptibility to, 9; cmm9 O14746
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#613073 Metaphyseal anadysplasia 2; mandp2 P14780
#601492 Mucopolysaccharidosis, type ix; mps9 Q12794
#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
#613796 Mycobacterial and viral infections, susceptibility to, autosomal recessive P42224
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#166350 Osseous heteroplasia, progressive; poh P63092
#167000 Ovarian cancer P38398
#614320 Pancreatic cancer, susceptibility to, 4; pnca4 P38398
#260500 Papilloma of choroid plexus; cpp P04637
#168600 Parkinson disease, late-onset; pd P04062
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#102200 Pituitary adenoma, growth hormone-secreting P63092
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#614278 Platelet-activating factor acetylhydrolase deficiency; pafad Q13093
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#614742 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1; pfbmft1 O14746
#178500 Pulmonary fibrosis, idiopathic; ipf O14746
#275210 Restrictive dermopathy, lethal P02545
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#602111 Spondyloepimetaphyseal dysplasia, missouri type P45452
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#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
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253
#112100 Yt blood group antigen P22303

KEGG DISEASE (102)

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)
H00764 Cri du chat syndrome O14746 (related)
H01132 Aplastic anemia (AA) O14746 (related)
H01299 Idiopathic pulmonary fibrosis O14746 (related)
H00022 Bladder cancer O14746 (marker)
P04637 (related)
H00024 Prostate cancer O14746 (marker)
P10275 (related)
H00081 Hashimoto's thyroiditis P01215 (marker)
H00082 Graves' disease P01215 (marker)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P01215 (marker)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
H00563 Emery-Dreifuss muscular dystrophy P02545 (related)
H00590 Congenital muscular dystrophies (CMD/MDC) P02545 (related)
H00593 Limb-girdle muscular dystrophy (LGMD) P02545 (related)
H00601 Hutchinson-Gilford progeria syndrome P02545 (related)
H00663 Restrictive dermopathy P02545 (related)
H00665 Mandibuloacral dysplasia P02545 (related)
H01216 Left ventricular noncompaction (LVNC) P02545 (related)
H00026 Endometrial Cancer P03372 (marker)
P04637 (related)
P06401 (marker)
H00028 Choriocarcinoma P03956 (related)
P04637 (related)
P08253 (related)
H00066 Lewy body dementia (LBD) P04062 (related)
H00126 Gaucher disease P04062 (related)
H00426 Defects in the degradation of ganglioside P04062 (related)
H00810 Progressive myoclonic epilepsy (PME) P04062 (related)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
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)
H00016 Oral cancer P04637 (related)
P04637 (marker)
P40763 (related)
H00017 Esophageal cancer P04637 (related)
P04637 (marker)
P35354 (related)
H00018 Gastric cancer 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)
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)
H00042 Glioma P04637 (related)
P04637 (marker)
H00044 Cancer of the anal canal P04637 (related)
H00046 Cholangiocarcinoma P04637 (related)
P35354 (related)
H00047 Gallbladder cancer P04637 (related)
H00048 Hepatocellular carcinoma P04637 (related)
H00055 Laryngeal cancer P04637 (related)
P04637 (marker)
H00881 Li-Fraumeni syndrome P04637 (related)
H01007 Choroid plexus papilloma P04637 (related)
H00021 Renal cell carcinoma P04637 (marker)
H00093 Combined immunodeficiencies (CIDs) P06239 (related)
H00472 Torg-Winchester syndrome P08253 (related)
H00069 Glycogen storage diseases (GSD) P10253 (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)
H00249 Thyroid hormone resistance syndrome P10828 (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)
P45452 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00107 Other well-defined immunodeficiency syndromes P40763 (related)
H00089 IFN-gamma/IL-12 axis P42224 (related)
H00363 Candidiasis P42224 (related)
H01109 Chronic mucocutaneous candidiasis (CMC) P42224 (related)
H00931 Growth hormone insensitivity with immunodeficiency P51692 (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)
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)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00133 Mucopolysaccharidosis type IX (MPS9) Q12794 (related)
H00421 Mucopolysaccharidosis (MPS) Q12794 (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)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

10 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D000647 Amnesia C00002752
D050197 Atherosclerosis C00031401
D001943 Breast Neoplasms C00031401
D005910 Glioma C00031401
D034381 Hearing Loss C00031401
D017379 Hypertrophy, Left Ventricular C00031401
D007951 Leukemia, Myeloid C00031401
D020324 Amnesia, Anterograde C00002772
D008107 Liver Diseases C00002772
D009203 Myocardial Infarction C00002772