| Organism name | Annona reticulata |
|---|---|
| Genus | Annona |
| Family | Annonaceae |
| Kingdom | Plantae |
| Linked NCBI taxonomy name | Annona reticulata |
|---|---|
| Linked NCBI taxonomy ID | 301862 |
| Linked level | species |
| Family in NCBI taxonomy | Annonaceae |
|---|---|
| ID | 22140 |
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
| Plant class | Magnoliophyta |
|---|---|
| ID | 3398 |
| Species | Activity |
|---|---|
| Annona reticulata L. | Anthelmintic |
| Annona reticulata L. | Anticancer |
| Annona reticulata L. | Antiinflammatory |
| Annona reticulata L. | Antineoplastic |
| Annona reticulata L. | Antitumor |
| Annona reticulata L. | Astringent |
| Annona reticulata L. | Cytotoxic |
| Annona reticulata L. | Insecticide |
| Annona reticulata L. | Pediculicide |
| Annona reticulata L. | Poison |
| Annona reticulata L. | Purgative |
| Annona reticulata L. | Tonic |
| Annona reticulata L. | Vermifuge |
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| Q14761 | Protein tyrosine phosphatase receptor type C-associated protein | Enzyme | C00001807 C00001861 C00001878 | 0 / 0 |
| P00352 | Retinal dehydrogenase 1 | Enzyme | C00001861 | 0 / 0 |
| P24941 | Cyclin-dependent kinase 2 | Cdc2 | C00025827 | 0 / 0 |
| P30926 | Neuronal acetylcholine receptor subunit beta-4 | CHRN beta | C00001878 | 0 / 0 |
| P32297 | Neuronal acetylcholine receptor subunit alpha-3 | CHRN alpha | C00001878 | 1 / 0 |
| P17787 | Neuronal acetylcholine receptor subunit beta-2 | CHRN beta | C00001878 | 1 / 1 |
| P43681 | Neuronal acetylcholine receptor subunit alpha-4 | CHRN alpha | C00001878 | 1 / 1 |
| Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00001861 | 1 / 0 |
| Q9BQF6 | Sentrin-specific protease 7 | Enzyme | C00001861 | 0 / 0 |
| Q9GZR1 | Sentrin-specific protease 6 | Enzyme | C00001861 | 0 / 0 |
| Q96LD8 | Sentrin-specific protease 8 | Enzyme | C00001861 | 0 / 0 |
| P42574 | Caspase-3 | C14 | C00001861 | 0 / 0 |
| O75496 | Geminin | Unclassified protein | C00001861 | 0 / 0 |
| P00734 | Prothrombin | S1A | C00025319 | 4 / 2 |
| Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00001861 | 3 / 3 |
| Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00001861 | 0 / 0 |
| P22303 | Acetylcholinesterase | Hydrolase | C00025231 | 1 / 0 |
| P35372 | Mu-type opioid receptor | Opioid receptor | C00001910 | 0 / 0 |
| Q9UNA4 | DNA polymerase iota | Enzyme | C00001861 | 0 / 0 |
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00001861 | 4 / 3 |
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00001861 | 0 / 0 |
| P43351 | DNA repair protein RAD52 homolog | Unclassified protein | C00001861 | 0 / 0 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
| #600513 | Epilepsy, nocturnal frontal lobe, 1; enfl1 |
P43681
|
| #605375 | Epilepsy, nocturnal frontal lobe, 3; enfl3 |
P17787
|
| #600274 | Frontotemporal dementia; ftd |
P10636
|
| #300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
| #300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
| #160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
| #260540 | Parkinson-dementia syndrome |
P10636
|
| #172700 | Pick disease of brain |
P10636
|
| #614390 | Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 |
P00734
|
| #613679 | Prothrombin deficiency, congenital |
P00734
|
| #612052 | Smoking as a quantitative trait locus 3; sqtl3 |
P32297
|
| #601367 | Stroke, ischemic |
P00734
|
| #601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
| #188050 | Thrombophilia due to thrombin defect; thph1 |
P00734
|
| #112100 | Yt blood group antigen |
P22303
|
| KEGG | name | UniProt |
|---|---|---|
| H00223 | Inherited thrombophilia |
P00734
(related)
|
| H01254 | Congenital prothrombin deficiency |
P00734
(related)
|
| H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
| H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
| H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
| H00807 | Autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) |
P17787
(related)
P43681 (related) |
| H00480 | Non-syndromic X-linked mental retardation |
Q99714
(related)
|
| H00658 | Syndromic X-linked mental retardation |
Q99714
(related)
|
| H00925 | 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency |
Q99714
(related)
|