| Organism name | Corsinia coriandrina | 
|---|---|
| Genus | |
| Family | |
| Kingdom | 
| Linked NCBI taxonomy name | Corsinia coriandra | 
|---|---|
| Linked NCBI taxonomy ID | 63791 | 
| Linked level | species | 
| Family in NCBI taxonomy | Corsiniaceae | 
|---|---|
| ID | 74540 | 
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae | 
|---|---|
| ID | 33090 | 
| Plant class | Embryophyta | 
|---|---|
| ID | 3193 | 
| 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 | 
|---|---|---|---|---|---|---|---|---|
| C00005375   | Quercetin 3-galacturonide | CHEMBL520546 CHEMBL1506682 | 23 / 30 / 21 | No. 2 | No. 15 |   | ||
| C00015321   | 3,4'-Dimethoxybibenzyl / Lunularine dimethyl ether | CHEMBL477915 | No. 96 | No. 26 |   | |||
| C00019227   | Corsifuran A / 5,4'-Dimethoxy-2,3-dihydro-2-arylbenzofuran | No. 179 | No. 15 |   | ||||
| C00019228   | Corsifuran B / 5-Hydroxy-4'-methoxy-2,3-dihydro-2-arylbenzofuran | No. 179 | No. 15 |   | ||||
| C00019229   | Corsifuran C / 5,4'-Dimethoxy-2-arylbenzofuran | No. 210 | No. 15 |   | ||||
| C00002889   | Lunularin / 3,4'-Dihydroxybibenzyl | CHEMBL445252 | C121619 | No. 242 | No. 26 |   | ||
| C00019230   | (E)-3,4'-Dimethoxystilbene / (E)-1-Methoxy-3-[2-(4-methoxyphenyl)ethenyl]-benzene | CHEMBL215583 CHEMBL244727 | No. 344 | No. 13 |   | |||
| C00019231   | (Z)-3,4'-Dimethoxystilbene / (Z)-1-Methoxy-3-[2-(4-methoxyphenyl)ethenyl]-benzene | CHEMBL215583 CHEMBL244727 | No. 344 | No. 13 |   | |||
| C00000212   | Lunularic acid | CHEMBL240495 | C067452 | No. 3522 | No. 26 |   | 
| accession | description | class description | KNApSAcK metabolite in interactions | # of diseases (OMIM / KEGG) | 
|---|---|---|---|---|
| Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00005375 | 0 / 0 | 
| P06746 | DNA polymerase beta | Enzyme | C00005375 | 0 / 0 | 
| P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00005375 | 1 / 1 | 
| Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00005375 | 0 / 0 | 
| P02545 | Prelamin-A/C | Unclassified protein | C00005375 | 11 / 10 | 
| Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00005375 | 1 / 0 | 
| P00352 | Retinal dehydrogenase 1 | Enzyme | C00005375 | 0 / 0 | 
| P39748 | Flap endonuclease 1 | Enzyme | C00005375 | 0 / 0 | 
| P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00005375 | 7 / 3 | 
| Q9Y253 | DNA polymerase eta | Enzyme | C00005375 | 1 / 1 | 
| P09923 | Intestinal-type alkaline phosphatase | Enzyme | C00005375 | 0 / 0 | 
| P05186 | Alkaline phosphatase, tissue-nonspecific isozyme | Enzyme | C00005375 | 3 / 1 | 
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00005375 | 0 / 0 | 
| P10696 | Alkaline phosphatase, placental-like | Enzyme | C00005375 | 0 / 1 | 
| Q9UNA4 | DNA polymerase iota | Enzyme | C00005375 | 0 / 0 | 
| O75164 | Lysine-specific demethylase 4A | Enzyme | C00005375 | 0 / 0 | 
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00005375 | 0 / 0 | 
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00005375 | 4 / 3 | 
| Q9UBT6 | DNA polymerase kappa | Enzyme | C00005375 | 0 / 0 | 
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00005375 | 0 / 0 | 
| Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00005375 | 0 / 0 | 
| O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00005375 | 0 / 0 | 
| Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00005375 | 2 / 1 | 
| OMIM | preferred title | UniProt | 
|---|---|---|
| #219080 | Acth-independent macronodular adrenal hyperplasia; aimah | P63092 | 
| #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 | Q14191 | 
| #181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 | P02545 | 
| #600274 | Frontotemporal dementia; ftd | P10636 | 
| #232300 | Glycogen storage disease ii | P10253 | 
| #610140 | Heart-hand syndrome, slovenian type | P02545 | 
| #176670 | Hutchinson-gilford progeria syndrome; hgps | P02545 | 
| #146300 | Hypophosphatasia, adult | P05186 | 
| #241510 | Hypophosphatasia, childhood | P05186 | 
| #241500 | Hypophosphatasia, infantile | P05186 | 
| #151660 | Lipodystrophy, familial partial, type 2; fpld2 | P02545 | 
| #248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada | P02545 | 
| #174800 | Mccune-albright syndrome; mas | P63092 | 
| #613205 | Muscular dystrophy, congenital, lmna-related | P02545 | 
| #159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b | P02545 | 
| #160900 | Myotonic dystrophy 1; dm1 | Q9NR56 | 
| #166350 | Osseous heteroplasia, progressive; poh | P63092 | 
| #260540 | Parkinson-dementia syndrome | P10636 | 
| #172700 | Pick disease of brain | P10636 | 
| #102200 | Pituitary adenoma, growth hormone-secreting | P63092 | 
| #103580 | Pseudohypoparathyroidism, type ia; php1a | P63092 | 
| #603233 | Pseudohypoparathyroidism, type ib; php1b | P63092 | 
| #612462 | Pseudohypoparathyroidism, type ic; php1c | P63092 | 
| #275210 | Restrictive dermopathy, lethal | P02545 | 
| #601104 | Supranuclear palsy, progressive, 1; psnp1 | P10636 | 
| #277700 | Werner syndrome; wrn | Q14191 | 
| #278750 | Xeroderma pigmentosum, variant type; xpv | Q9Y253 | 
| KEGG | name | UniProt | 
|---|---|---|
| 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) | 
| H00213 | Hypophosphatasia | P05186
                            (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) | 
| H00244 | Pseudohypoparathyroidism | P63092
                            (related) | 
| H00441 | Progressive osseous heteroplasia (POH) | P63092
                            (related) | 
| H00501 | Fibrous dysplasia, polyostotic | P63092
                            (related) | 
| H00296 | Defects in RecQ helicases | Q14191
                            (related) | 
| H00403 | Disorders of nucleotide excision repair | Q9Y253
                            (related) |