| Organism name | Rhus javanica | 
|---|---|
| Genus | Rhus | 
| Family | Anacardiaceae | 
| Kingdom | Plantae | 
| Linked NCBI taxonomy name | Brucea javanica | 
|---|---|
| Linked NCBI taxonomy ID | 210348 | 
| Linked level | species | 
| Family in NCBI taxonomy | Simaroubaceae | 
|---|---|
| ID | 23808 | 
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae | 
|---|---|
| ID | 33090 | 
| Plant class | rosids | 
|---|---|
| ID | 71275 | 
| 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 | 
|---|---|---|---|---|---|---|---|---|
| C00032984   | Fouquierone / (+)-Fouquierone | CHEMBL224814 | No. 23 | No. 51 |   | |||
| C00033061   | Isofouquierone peroxide / (+)-Isofouquierone peroxide | No. 23 | No. 51 |   | ||||
| C00006941   | Butein | CHEMBL128000 | C040918 | 17 / 31 / 34 | 8 / 0 | No. 92 | No. 13 |   | 
| C00008026   | Sulfuretin / Sulphuretin / 6,3',4'-Trihydroxyaurone | CHEMBL490355 CHEMBL513487 | C054989 | 42 / 37 / 34 | No. 450 | No. 13 |   | |
| C00033379   | Semialatic acid | No. 827 |   | 
| accession | description | class description | KNApSAcK metabolite in interactions | # of diseases (OMIM / KEGG) | 
|---|---|---|---|---|
| P11473 | Vitamin D3 receptor | NR1I1 | C00006941 C00008026 | 2 / 3 | 
| O00255 | Menin | Unclassified protein | C00006941 C00008026 | 2 / 5 | 
| Q9UBT6 | DNA polymerase kappa | Enzyme | C00006941 C00008026 | 0 / 0 | 
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00006941 C00008026 | 0 / 0 | 
| P11021 | 78 kDa glucose-regulated protein | Unclassified protein | C00006941 C00008026 | 0 / 0 | 
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00006941 C00008026 | 1 / 2 | 
| P12931 | Proto-oncogene tyrosine-protein kinase Src | Src | C00006941 | 0 / 0 | 
| P24941 | Cyclin-dependent kinase 2 | Cdc2 | C00006941 | 0 / 0 | 
| Q9HBX9 | Relaxin receptor 1 | Relaxin receptor | C00008026 | 0 / 0 | 
| Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00008026 | 1 / 0 | 
| P00533 | Epidermal growth factor receptor | TK tyrosine-protein kinase EGFR subfamily | C00006941 | 1 / 8 | 
| Q07820 | Induced myeloid leukemia cell differentiation protein Mcl-1 | Other cytosolic protein | C00008026 | 0 / 0 | 
| P47901 | Vasopressin V1b receptor | Vasopressin and oxytocin receptor | C00008026 | 0 / 0 | 
| P39748 | Flap endonuclease 1 | Enzyme | C00008026 | 0 / 0 | 
| Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00008026 | 0 / 0 | 
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00008026 | 2 / 0 | 
| P38398 | Breast cancer type 1 susceptibility protein | Enzyme | C00008026 | 4 / 2 | 
| P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00008026 | 0 / 0 | 
| P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00008026 | 7 / 3 | 
| Q9Y253 | DNA polymerase eta | Enzyme | C00008026 | 1 / 1 | 
| P09923 | Intestinal-type alkaline phosphatase | Enzyme | C00008026 | 0 / 0 | 
| P05186 | Alkaline phosphatase, tissue-nonspecific isozyme | Enzyme | C00008026 | 3 / 1 | 
| P11308 | Transcriptional regulator ERG | Unclassified protein | C00008026 | 1 / 2 | 
| Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00008026 | 0 / 0 | 
| Q9HC16 | DNA dC->dU-editing enzyme APOBEC-3G | Enzyme | C00008026 | 0 / 0 | 
| P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00008026 | 1 / 1 | 
| P10828 | Thyroid hormone receptor beta | NR1A2 | C00008026 | 3 / 1 | 
| P35968 | Vascular endothelial growth factor receptor 2 | Vegfr | C00006941 | 1 / 0 | 
| P08581 | Hepatocyte growth factor receptor | TK tyrosine-protein kinase MET subfamily | C00006941 | 2 / 3 | 
| P10696 | Alkaline phosphatase, placental-like | Enzyme | C00008026 | 0 / 1 | 
| P08253 | 72 kDa type IV collagenase | M10A | C00008026 | 1 / 3 | 
| O15118 | Niemann-Pick C1 protein | Unclassified protein | C00008026 | 1 / 1 | 
| Q8WXD0 | Relaxin receptor 2 | Relaxin receptor | C00008026 | 1 / 1 | 
| Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00008026 | 0 / 0 | 
| P11362 | Fibroblast growth factor receptor 1 | Fgfr | C00006941 | 4 / 5 | 
| Q9UNA4 | DNA polymerase iota | Enzyme | C00008026 | 0 / 0 | 
| P04062 | Glucosylceramidase | Enzyme | C00006941 | 6 / 4 | 
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00008026 | 4 / 3 | 
| P10721 | Mast/stem cell growth factor receptor Kit | Pdgfr | C00006941 | 4 / 3 | 
| P21802 | Fibroblast growth factor receptor 2 | TK tyrosine-protein kinase TLK subfamily | C00006941 | 9 / 3 | 
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00008026 | 0 / 0 | 
| P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00008026 | 0 / 0 | 
| Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00008026 | 0 / 0 | 
| Q8IUX4 | DNA dC->dU-editing enzyme APOBEC-3F | Enzyme | C00008026 | 0 / 0 | 
| O00487 | 26S proteasome non-ATPase regulatory subunit 14 | Enzyme | C00008026 | 0 / 0 | 
| Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00008026 | 0 / 0 | 
| Q13951 | Core-binding factor subunit beta | Unclassified protein | C00008026 | 0 / 1 | 
| Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00008026 | 1 / 4 | 
| P23219 | Prostaglandin G/H synthase 1 | Oxidoreductase | C00006941 | 0 / 0 | 
| P35354 | Prostaglandin G/H synthase 2 | Oxidoreductase | C00006941 | 0 / 3 | 
| O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00008026 | 0 / 0 | 
| Q9H0H5 | Rac GTPase-activating protein 1 | Unclassified protein | C00008026 | 0 / 0 | 
| Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00008026 | 2 / 1 | 
| gene | gene name | gene description | KNApSAcK metabolite in interactions | 
|---|---|---|---|
| 207 | AKT1, AKT, CWS6, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA | v-akt murine thymoma viral oncogene homolog 1 (EC:2.7.11.1) | C00006941 | 
| 1734 | DIO2, 5DII, D2, DIOII, SelY, TXDI2 | deiodinase, iodothyronine, type II (EC:1.97.1.10) | C00006941 | 
| 4318 | MMP9, CLG4B, GELB, MANDP2, MMP-9 | matrix metallopeptidase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase) (EC:3.4.24.35) | C00006941 | 
| 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 | C00006941 | 
| 5970 | RELA, NFKB3, p65 | v-rel avian reticuloendotheliosis viral oncogene homolog A | C00006941 | 
| 23411 | SIRT1, SIR2L1 | sirtuin 1 | C00006941 | 
| 7124 | TNF, DIF, TNF-alpha, TNFA, TNFSF2 | tumor necrosis factor | C00006941 | 
| 7422 | VEGFA, MVCD1, VEGF, VPF | vascular endothelial growth factor A | C00006941 | 
| OMIM | preferred title | UniProt | 
|---|---|---|
| #219080 | Acth-independent macronodular adrenal hyperplasia; aimah | P63092 | 
| #207410 | Antley-bixler syndrome without genital anomalies or disordered steroidogenesis; abs2 | P21802 | 
| #101200 | Apert syndrome | P21802 | 
| #123790 | Beare-stevenson cutis gyrata syndrome; bstvs | P21802 | 
| #614592 | Bent bone dysplasia syndrome; bbds | P21802 | 
| #114480 | Breast cancer | P38398 | 
| #604370 | Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 | P38398 | 
| #114500 | Colorectal cancer; crc | P84022 Q14191 | 
| #123500 | Crouzon syndrome | P21802 | 
| #219050 | Cryptorchidism, unilateral or bilateral | Q8WXD0 | 
| #612219 | Ewing sarcoma; es | P11308 | 
| #600274 | Frontotemporal dementia; ftd | P10636 | 
| #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 | 
| #232300 | Glycogen storage disease ii | P10253 | 
| #605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay | Q03164 | 
| #602089 | Hemangioma, capillary infantile | P35968 | 
| #114550 | Hepatocellular carcinoma | P08581 | 
| #145000 | Hyperparathyroidism 1; hrpt1 | O00255 | 
| #147950 | Hypogonadotropic hypogonadism 2 with or without anosmia; hh2 | P11362 | 
| #146300 | Hypophosphatasia, adult | P05186 | 
| #241510 | Hypophosphatasia, childhood | P05186 | 
| #241500 | Hypophosphatasia, infantile | P05186 | 
| #123150 | Jackson-weiss syndrome; jws | P21802 | 
| #149730 | Lacrimoauriculodentodigital syndrome; ladd | P21802 | 
| #601626 | Leukemia, acute myeloid; aml | P10721 | 
| #613795 | Loeys-dietz syndrome, type 3; lds3 | P84022 | 
| #211980 | Lung cancer | P00533 | 
| #174800 | Mccune-albright syndrome; mas | P63092 | 
| #259600 | Multicentric osteolysis, nodulosis, and arthropathy; mona | P08253 | 
| #131100 | Multiple endocrine neoplasia, type i; men1 | O00255 | 
| #607948 | Mycobacterium tuberculosis, susceptibility to | P11473 | 
| #160900 | Myotonic dystrophy 1; dm1 | Q9NR56 | 
| #257220 | Niemann-pick disease, type c1; npc1 | O15118 | 
| #166350 | Osseous heteroplasia, progressive; poh | P63092 | 
| #166250 | Osteoglophonic dysplasia; ogd | P11362 | 
| #167000 | Ovarian cancer | P38398 | 
| #614320 | Pancreatic cancer, susceptibility to, 4; pnca4 | P38398 | 
| #168600 | Parkinson disease, late-onset; pd | P04062 | 
| #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 | 
| #601399 | Platelet disorder, familial, with associated myeloid malignancy | Q01196 | 
| #103580 | Pseudohypoparathyroidism, type ia; php1a | P63092 | 
| #603233 | Pseudohypoparathyroidism, type ib; php1b | P63092 | 
| #612462 | Pseudohypoparathyroidism, type ic; php1c | P63092 | 
| #605074 | Renal cell carcinoma, papillary, 1; rccp1 | P08581 | 
| #609579 | Scaphocephaly, maxillary retrusion, and mental retardation | P21802 | 
| #601104 | Supranuclear palsy, progressive, 1; psnp1 | P10636 | 
| #273300 | Testicular germ cell tumor; tgct | P10721 | 
| #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 | 
| #277700 | Werner syndrome; wrn | Q14191 | 
| #278750 | Xeroderma pigmentosum, variant type; xpv | Q9Y253 | 
| KEGG | name | UniProt | 
|---|---|---|
| H00033 | Adrenal carcinoma | O00255
                            (related) | 
| H00034 | Carcinoid | O00255
                            (related) | 
| H00045 | Malignant islet cell carcinoma | O00255
                            (related) | 
| H00246 | Primary hyperparathyroidism | O00255
                            (related) | 
| H01102 | Pituitary adenomas | O00255
                            (related) | 
| H00136 | Niemann-Pick disease type C (NPC) | O15118
                            (related) | 
| H00016 | Oral cancer | P00533
                            (related) P00533 (marker) | 
| H00017 | Esophageal cancer | P00533
                            (related) P35354 (related) | 
| H00018 | Gastric cancer | P00533
                            (related) P08581 (related) P21802 (related) | 
| H00022 | Bladder cancer | P00533
                            (related) | 
| H00028 | Choriocarcinoma | P00533
                            (related) P08253 (related) | 
| H00030 | Cervical cancer | P00533
                            (related) | 
| H00042 | Glioma | P00533
                            (related) P00533 (marker) | 
| H00055 | Laryngeal cancer | P00533
                            (related) P00533 (marker) | 
| H00066 | Lewy body dementia (LBD) | P04062
                            (related) | 
| H00126 | Gaucher disease | P04062
                            (related) | 
| H00426 | Defects in the degradation of ganglioside | P04062
                            (related) | 
| H00810 | Progressive myoclonic epilepsy (PME) | P04062
                            (related) | 
| H00213 | Hypophosphatasia | P05186
                            (related) | 
| H00025 | Penile cancer | P08253
                            (related) P35354 (related) | 
| H00472 | Torg-Winchester syndrome | P08253
                            (related) | 
| H00021 | Renal cell carcinoma | P08581
                            (related) | 
| H00046 | Cholangiocarcinoma | P08581
                            (related) P35354 (related) | 
| H00069 | Glycogen storage diseases (GSD) | P10253
                            (related) | 
| H00058 | Amyotrophic lateral sclerosis (ALS) | P10636
                            (related) | 
| H00077 | Progressive supranuclear palsy (PSP) | P10636
                            (related) | 
| H00078 | Frontotemporal lobar degeneration (FTLD) | P10636
                            (related) | 
| H00023 | Testicular cancer | P10696
                            (marker) P10721 (marker) | 
| H00003 | Acute myeloid leukemia (AML) | P10721
                            (related) P10721 (marker) Q01196 (related) Q01196 (marker) Q13951 (marker) | 
| H00170 | Piebaldism | P10721
                            (related) | 
| H00249 | Thyroid hormone resistance syndrome | P10828
                            (related) | 
| H00024 | Prostate cancer | P11308
                            (related) | 
| H00035 | Ewing's sarcoma | P11308
                            (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) | 
| H00642 | Lacrimo-auriculo-dento-digital syndrome (LADD) | P21802
                            (related) | 
| H00027 | Ovarian cancer | P38398
                            (related) | 
| H00031 | Breast cancer | P38398
                            (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) | 
| H00004 | Chronic myeloid leukemia (CML) | Q01196
                            (related) | 
| H00978 | Thrombocytopenia (THC) | Q01196
                            (related) | 
| H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) | Q03164
                            (related) | 
| H00296 | Defects in RecQ helicases | Q14191
                            (related) | 
| H00609 | 46,XY disorders of sex development (Other) | Q8WXD0
                            (related) | 
| H00403 | Disorders of nucleotide excision repair | Q9Y253
                            (related) |