| Organism name | Callicarpa formosana | 
|---|---|
| Genus | Callicarpa | 
| Family | Labiatae | 
| Kingdom | Plantae | 
| Linked NCBI taxonomy name | Callicarpa formosana | 
|---|---|
| Linked NCBI taxonomy ID | 886264 | 
| Linked level | species | 
| Family in NCBI taxonomy | Lamiaceae | 
|---|---|
| ID | 4136 | 
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae | 
|---|---|
| ID | 33090 | 
| Plant class | asterids | 
|---|---|
| ID | 71274 | 
| 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 | 
|---|---|---|---|---|---|---|---|---|
| C00004655   | Quercetin pentamethyl ether / 3,5,7,3',4'-Pentamethoxyflavone | CHEMBL19032 | 16 / 10 / 12 | No. 8 | No. 15 |   | ||
| C00029633   | Ursolic acid / Acetylursolic acid | CHEMBL55086 CHEMBL410525 | 4 / 2 / 2 | No. 177 |   | 
| accession | description | class description | KNApSAcK metabolite in interactions | # of diseases (OMIM / KEGG) | 
|---|---|---|---|---|
| P33527 | Multidrug resistance-associated protein 1 | drugs | C00004655 | 0 / 0 | 
| P06746 | DNA polymerase beta | Enzyme | C00029633 | 0 / 0 | 
| Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00004655 | 0 / 0 | 
| Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00004655 | 1 / 0 | 
| P00352 | Retinal dehydrogenase 1 | Enzyme | C00004655 | 0 / 0 | 
| P17405 | Sphingomyelin phosphodiesterase | Enzyme | C00004655 | 2 / 2 | 
| P39748 | Flap endonuclease 1 | Enzyme | C00004655 | 0 / 0 | 
| P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00004655 | 0 / 0 | 
| Q12791 | Calcium-activated potassium channel subunit alpha-1 | KCNM, KCa1.x | C00004655 | 1 / 1 | 
| P11511 | Cytochrome P450 19A1 | Cytochrome P450 19A1 | C00029633 | 2 / 2 | 
| P28482 | Mitogen-activated protein kinase 1 | Erk | C00004655 | 0 / 0 | 
| Q9UNQ0 | ATP-binding cassette sub-family G member 2 | ATP binding cassette | C00004655 | 2 / 0 | 
| Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00004655 | 0 / 0 | 
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00004655 | 0 / 1 | 
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00029633 | 0 / 0 | 
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00004655 | 0 / 0 | 
| P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00029633 | 0 / 0 | 
| Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00004655 | 1 / 1 | 
| O00255 | Menin | Unclassified protein | C00004655 | 2 / 5 | 
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00004655 | 1 / 2 | 
| OMIM | preferred title | UniProt | 
|---|---|---|
| #613546 | Aromatase deficiency | P11511 | 
| #139300 | Aromatase excess syndrome; aexs | P11511 | 
| #614490 | Blood group, junior system; jr | Q9UNQ0 | 
| #609446 | Generalized epilepsy and paroxysmal dyskinesia; gepd | Q12791 | 
| #605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay | Q03164 | 
| #145000 | Hyperparathyroidism 1; hrpt1 | O00255 | 
| #131100 | Multiple endocrine neoplasia, type i; men1 | O00255 | 
| #160900 | Myotonic dystrophy 1; dm1 | Q9NR56 | 
| #257200 | Niemann-pick disease, type a | P17405 | 
| #607616 | Niemann-pick disease, type b | P17405 | 
| #607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 | Q9NUW8 | 
| #138900 | Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 | Q9UNQ0 | 
| 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) | 
| H00036 | Osteosarcoma | P08684
                            (marker) | 
| H00599 | 46,XX disorders of sex development (Disorders related to androgen excess) | P11511
                            (related) | 
| H00794 | Aromatase excess syndrome | P11511
                            (related) | 
| H00137 | Niemann-Pick disease (NPD) typeA and B | P17405
                            (related) | 
| H00424 | Defects in the degradation of sphingomyelin | P17405
                            (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) | 
| H01258 | Generalized epilepsy and paroxysmal dyskinesia (GEPD) | Q12791
                            (related) | 
| H00063 | Spinocerebellar ataxia (SCA) | Q9NUW8
                            (related) |