| Organism name | Marchantia berteroana |
|---|---|
| Genus | Marchantia |
| Family | Marchantiaceae |
| Kingdom | Plantae |
| Linked NCBI taxonomy name | Marchantia |
|---|---|
| Linked NCBI taxonomy ID | 3196 |
| Linked level | genus |
| Family in NCBI taxonomy | Marchantiaceae |
|---|---|
| ID | 29585 |
| 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 |
|---|---|---|---|---|---|---|---|---|
|
C00004302
|
Luteolin 3',4'-digalacturonide
|
No. 1 | No. 15 |
|
||||
|
C00004423
|
8-Hydroxyluteolin 8,4'-diglucuronide
|
No. 1 | No. 15 |
|
||||
|
C00004293
|
Luteolin 7,3'-digalacturonide
|
No. 1 | No. 15 |
|
||||
|
C00004269
|
Luteolin 7-galacturonide
|
CHEMBL464224
|
No. 2 | No. 15 |
|
|||
|
C00004246
|
Isoscutellarein 8-glucuronide
|
CHEMBL462705
|
No. 2 | No. 15 |
|
|||
|
C00004420
|
8-Hydroxyluteolin 8-glucuronide
|
CHEMBL512433
|
No. 2 | No. 15 |
|
|||
|
C00004145
|
Apigenin 7-galacturonide
|
CHEMBL254213
CHEMBL1980748 |
No. 2 | No. 15 |
|
|||
|
C00004275
|
Luteolin 3'-galacturonide
|
No. 2 | No. 15 |
|
||||
|
C00008048
|
Aureusidin 6-glucuronide
|
No. 12 | No. 14 |
|
||||
|
C00002889
|
Lunularin
/ 3,4'-Dihydroxybibenzyl |
CHEMBL445252
|
C121619
|
No. 242 | No. 26 |
|
||
|
C00001120
|
D-Galacturonic acid
|
CHEMBL496672
CHEMBL1159524 CHEMBL2068684 |
13 / 14 / 14 | No. 4351 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00001120 | 1 / 0 |
| P02545 | Prelamin-A/C | Unclassified protein | C00001120 | 11 / 10 |
| P02768 | Serum albumin | Secreted protein | C00001120 | 0 / 0 |
| P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00001120 | 0 / 1 |
| Q16665 | Hypoxia-inducible factor 1-alpha | Transcription Factor | C00001120 | 0 / 0 |
| O75496 | Geminin | Unclassified protein | C00001120 | 0 / 0 |
| Q8TCC7 | Solute carrier family 22 member 8 | Antiporter | C00001120 | 0 / 0 |
| P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00001120 | 0 / 0 |
| P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00001120 | 1 / 1 |
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00001120 | 0 / 1 |
| Q9UNA4 | DNA polymerase iota | Enzyme | C00001120 | 0 / 0 |
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00001120 | 0 / 0 |
| Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00001120 | 1 / 1 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
| #212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
| #605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
| #609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
| #608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
| #181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
| #610140 | Heart-hand syndrome, slovenian type |
P02545
|
| #176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
| #151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
| #248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
| #613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
| #159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
| #275210 | Restrictive dermopathy, lethal |
P02545
|
| #607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
| 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)
|
| H00036 | Osteosarcoma |
P08684
(marker)
|
| H01205 | Coumarin resistance |
P11712
(related)
|
| H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
| H00063 | Spinocerebellar ataxia (SCA) |
Q9NUW8
(related)
|