| Organism name | Wyethia angustifolia |
|---|---|
| Genus | Wyethia |
| Family | Asteraceae |
| Kingdom | Plantae |
| Linked NCBI taxonomy name | Wyethia angustifolia |
|---|---|
| Linked NCBI taxonomy ID | 230214 |
| Linked level | species |
| Family in NCBI taxonomy | Asteraceae |
|---|---|
| ID | 4210 |
| 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 |
|---|---|---|---|---|---|---|---|---|
|
C00009890
|
5,7,3',4'-Tetrahydroxy-6-prenylisoflavone
|
No. 15 | No. 15 |
|
||||
|
C00008453
|
5,7-Dihydroxy-4'-methoxy-8-C-prenylflavanone
|
CHEMBL556429
|
1 / 2 / 0 | No. 28 | No. 14 |
|
||
|
C00000997
|
6-Prenylnaringenin
|
CHEMBL1537093
|
14 / 16 / 16 | No. 28 | No. 14 |
|
||
|
C00008640
|
3,5,7,4'-Tetrahydroxy-3'-methoxy-8-prenylflavanone
|
No. 276 | No. 14 |
|
||||
|
C00008637
|
7,8-Dihydrooxepinodihydroquercetin
|
No. 276 | No. 14 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P04062 | Glucosylceramidase | Enzyme | C00000997 | 6 / 4 |
| Q13315 | Serine-protein kinase ATM | Atypical serine/threonine protein kinase PIKK subfamily | C00000997 | 1 / 4 |
| Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00000997 | 0 / 0 |
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00000997 | 2 / 0 |
| O75496 | Geminin | Unclassified protein | C00000997 | 0 / 0 |
| P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00000997 | 0 / 0 |
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00000997 | 1 / 2 |
| P28482 | Mitogen-activated protein kinase 1 | Erk | C00000997 | 0 / 0 |
| Q9UNQ0 | ATP-binding cassette sub-family G member 2 | ATP binding cassette | C00008453 | 2 / 0 |
| Q6W5P4 | Neuropeptide S receptor | Neuropeptide receptor | C00000997 | 1 / 0 |
| O75164 | Lysine-specific demethylase 4A | Enzyme | C00000997 | 0 / 0 |
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00000997 | 0 / 0 |
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00000997 | 4 / 3 |
| Q13951 | Core-binding factor subunit beta | Unclassified protein | C00000997 | 0 / 1 |
| Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00000997 | 1 / 4 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #608584 | Asthma-related traits, susceptibility to, 2 |
Q6W5P4
|
| #208900 | Ataxia-telangiectasia; at |
Q13315
|
| #614490 | Blood group, junior system; jr |
Q9UNQ0
|
| #114500 | Colorectal cancer; crc |
P84022
|
| #600274 | Frontotemporal dementia; ftd |
P10636
|
| #608013 | Gaucher disease, perinatal lethal |
P04062
|
| #230800 | Gaucher disease, type i |
P04062
|
| #230900 | Gaucher disease, type ii |
P04062
|
| #231000 | Gaucher disease, type iii |
P04062
|
| #231005 | Gaucher disease, type iiic |
P04062
|
| #605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
| #613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
| #168600 | Parkinson disease, late-onset; pd |
P04062
|
| #260540 | Parkinson-dementia syndrome |
P10636
|
| #172700 | Pick disease of brain |
P10636
|
| #601399 | Platelet disorder, familial, with associated myeloid malignancy |
Q01196
|
| #601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
| #138900 | Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 |
Q9UNQ0
|
| KEGG | name | UniProt |
|---|---|---|
| H00066 | Lewy body dementia (LBD) |
P04062
(related)
|
| H00126 | Gaucher disease |
P04062
(related)
|
| H00426 | Defects in the degradation of ganglioside |
P04062
(related)
|
| H00810 | Progressive myoclonic epilepsy (PME) |
P04062
(related)
|
| H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
| H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
| H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(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)
|
| H00005 | Chronic lymphocytic leukemia (CLL) |
Q13315
(related)
|
| H00064 | Ataxia telangiectasia (AT) |
Q13315
(related)
|
| H00094 | DNA repair defects |
Q13315
(related)
|
| H00848 | Ataxia with ocular apraxia (AOA) |
Q13315
(related)
|