| Organism name | Strophioblachia fimbricalyx Boerl | 
|---|---|
| Genus | Strophioblachia | 
| Family | Euphorbiaceae | 
| Kingdom | Plantae | 
| Linked NCBI taxonomy name | Strophioblachia | 
|---|---|
| Linked NCBI taxonomy ID | 179701 | 
| Linked level | genus | 
| Family in NCBI taxonomy | Euphorbiaceae | 
|---|---|
| ID | 3977 | 
| 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 | 
|---|---|---|---|---|---|---|---|---|
| C00006268   | Spinosin | C055669 | No. 1 | No. 15 |   | |||
| C00001017   | Cosmosiin / Apigenin 7-glucoside / (-)-Apigenin 7-glucoside / Apigenin 7-O-beta-D-glucopyranoside | CHEMBL487995 CHEMBL487017 CHEMBL1591566 CHEMBL2165585 | C057792 | 5 / 6 / 1 | No. 2 | No. 15 |   | |
| C00001059   | Isovitexin / Saponaretin / Homovitexin / 6-C-beta-D-Glucopyranosylapigenin / 6-beta-D-Glucopyranosyl-4',5,7-trihydroxyflavone / 6-beta-D-Glucopyranosyl-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one | CHEMBL465360 CHEMBL1601394 | C049772 | 28 / 20 / 19 | No. 22 | No. 15 |   | |
| C00029499   | 3-Hydroxy-5,6-epoxy-beta-ionol 9-O-beta-D-glucopyranoside | CHEMBL1814430 | No. 153 |   | ||||
| C00029682   | Ampelopsisionoside | CHEMBL1311580 | 10 / 5 / 4 | No. 153 |   | |||
| C00029857   | Bridelionoside B | CHEMBL1643085 | No. 153 |   | 
| accession | description | class description | KNApSAcK metabolite in interactions | # of diseases (OMIM / KEGG) | 
|---|---|---|---|---|
| Q9UBT6 | DNA polymerase kappa | Enzyme | C00001017 C00001059 C00029682 | 0 / 0 | 
| P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00001059 C00029682 | 1 / 1 | 
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00001059 C00029682 | 0 / 0 | 
| P06746 | DNA polymerase beta | Enzyme | C00001059 C00029682 | 0 / 0 | 
| Q9UNA4 | DNA polymerase iota | Enzyme | C00001059 C00029682 | 0 / 0 | 
| Q9Y253 | DNA polymerase eta | Enzyme | C00001059 C00029682 | 1 / 1 | 
| Q9UNQ0 | ATP-binding cassette sub-family G member 2 | ATP binding cassette | C00001017 | 2 / 0 | 
| P17405 | Sphingomyelin phosphodiesterase | Enzyme | C00001059 | 2 / 2 | 
| P39748 | Flap endonuclease 1 | Enzyme | C00001059 | 0 / 0 | 
| O75496 | Geminin | Unclassified protein | C00029682 | 0 / 0 | 
| P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00001059 | 7 / 3 | 
| Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00001059 | 1 / 0 | 
| P09923 | Intestinal-type alkaline phosphatase | Enzyme | C00029682 | 0 / 0 | 
| P05186 | Alkaline phosphatase, tissue-nonspecific isozyme | Enzyme | C00029682 | 3 / 1 | 
| Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | C00001059 | 0 / 0 | 
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00001017 | 0 / 0 | 
| O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00001017 | 0 / 0 | 
| P10696 | Alkaline phosphatase, placental-like | Enzyme | C00029682 | 0 / 1 | 
| P00352 | Retinal dehydrogenase 1 | Enzyme | C00001059 | 0 / 0 | 
| Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00001059 | 0 / 0 | 
| P30989 | Neurotensin receptor type 1 | Neurotensin receptor | C00001059 | 0 / 0 | 
| Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00001059 | 0 / 0 | 
| O75164 | Lysine-specific demethylase 4A | Enzyme | C00001059 | 0 / 0 | 
| Q16637 | Survival motor neuron protein | Unclassified protein | C00001017 | 4 / 1 | 
| Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00001059 | 0 / 0 | 
| Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00001059 | 0 / 0 | 
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00001059 | 0 / 0 | 
| P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00001059 | 0 / 0 | 
| Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00001059 | 1 / 1 | 
| O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00001059 | 1 / 0 | 
| O00255 | Menin | Unclassified protein | C00001059 | 2 / 5 | 
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00001059 | 1 / 2 | 
| Q13951 | Core-binding factor subunit beta | Unclassified protein | C00001059 | 0 / 1 | 
| Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00001059 | 1 / 4 | 
| O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00001059 | 0 / 0 | 
| Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00001059 | 2 / 1 | 
| OMIM | preferred title | UniProt | 
|---|---|---|
| #219080 | Acth-independent macronodular adrenal hyperplasia; aimah | P63092 | 
| #614490 | Blood group, junior system; jr | Q9UNQ0 | 
| #114500 | Colorectal cancer; crc | Q14191 | 
| #137800 | Glioma susceptibility 1; glm1 | O75874 | 
| #232300 | Glycogen storage disease ii | P10253 | 
| #605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay | Q03164 | 
| #145000 | Hyperparathyroidism 1; hrpt1 | O00255 | 
| #146300 | Hypophosphatasia, adult | P05186 | 
| #241510 | Hypophosphatasia, childhood | P05186 | 
| #241500 | Hypophosphatasia, infantile | P05186 | 
| #174800 | Mccune-albright syndrome; mas | P63092 | 
| #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 | 
| #166350 | Osseous heteroplasia, progressive; poh | P63092 | 
| #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 | 
| #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 | 
| #607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 | Q9NUW8 | 
| #138900 | Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 | Q9UNQ0 | 
| #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) | 
| H00213 | Hypophosphatasia | P05186
                            (related) | 
| H00069 | Glycogen storage diseases (GSD) | P10253
                            (related) | 
| H00023 | Testicular cancer | P10696
                            (marker) | 
| H00137 | Niemann-Pick disease (NPD) typeA and B | P17405
                            (related) | 
| H00424 | Defects in the degradation of sphingomyelin | P17405
                            (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) | 
| 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) | 
| H00455 | Spinal muscular atrophy (SMA) | Q16637
                            (related) | 
| H00063 | Spinocerebellar ataxia (SCA) | Q9NUW8
                            (related) | 
| H00403 | Disorders of nucleotide excision repair | Q9Y253
                            (related) |