| Organism name | Diospyros lycioides |
|---|---|
| Genus | Diospyros |
| Family | Ebenaceae |
| Kingdom | Plantae |
| Linked NCBI taxonomy name | Royena lycioides |
|---|---|
| Linked NCBI taxonomy ID | 268841 |
| Linked level | species |
| Family in NCBI taxonomy | Ebenaceae |
|---|---|
| ID | 19955 |
| 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 |
|---|---|---|---|---|---|---|---|---|
|
C00043693
|
Mamegakinone
|
No. 312 |
|
|||||
|
C00043720
|
Methylnaphthazarin
|
CHEMBL11475
|
20 / 15 / 15 | No. 1047 | No. 80 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00043720 | 0 / 0 |
| P06746 | DNA polymerase beta | Enzyme | C00043720 | 0 / 0 |
| P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00043720 | 1 / 1 |
| O75604 | Ubiquitin carboxyl-terminal hydrolase 2 | Enzyme | C00043720 | 0 / 0 |
| P10828 | Thyroid hormone receptor beta | NR1A2 | C00043720 | 3 / 1 |
| P54132 | Bloom syndrome protein | Enzyme | C00043720 | 1 / 2 |
| Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00043720 | 1 / 0 |
| P00352 | Retinal dehydrogenase 1 | Enzyme | C00043720 | 0 / 0 |
| Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00043720 | 0 / 0 |
| P51151 | Ras-related protein Rab-9A | Unclassified protein | C00043720 | 0 / 0 |
| Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | C00043720 | 0 / 0 |
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00043720 | 1 / 2 |
| P28482 | Mitogen-activated protein kinase 1 | Erk | C00043720 | 0 / 0 |
| O15118 | Niemann-Pick C1 protein | Unclassified protein | C00043720 | 1 / 1 |
| Q6W5P4 | Neuropeptide S receptor | Neuropeptide receptor | C00043720 | 1 / 0 |
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00043720 | 0 / 0 |
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00043720 | 4 / 3 |
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00043720 | 0 / 0 |
| P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00043720 | 0 / 0 |
| O00255 | Menin | Unclassified protein | C00043720 | 2 / 5 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #608584 | Asthma-related traits, susceptibility to, 2 |
Q6W5P4
|
| #210900 | Bloom syndrome; blm |
P54132
|
| #600274 | Frontotemporal dementia; ftd |
P10636
|
| #232300 | Glycogen storage disease ii |
P10253
|
| #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
|
| #257220 | Niemann-pick disease, type c1; npc1 |
O15118
|
| #260540 | Parkinson-dementia syndrome |
P10636
|
| #172700 | Pick disease of brain |
P10636
|
| #601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
| #188570 | Thyroid hormone resistance, generalized, autosomal dominant; grth |
P10828
|
| #274300 | Thyroid hormone resistance, generalized, autosomal recessive; grth |
P10828
|
| #145650 | Thyroid hormone resistance, selective pituitary; prth |
P10828
|
| 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)
|
| H00136 | Niemann-Pick disease type C (NPC) |
O15118
(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)
|
| H00249 | Thyroid hormone resistance syndrome |
P10828
(related)
|
| H00094 | DNA repair defects |
P54132
(related)
|
| H00296 | Defects in RecQ helicases |
P54132
(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)
|