Organism name | Balsamorhiza macrophylla |
---|---|
Genus | Balsamorhiza |
Family | Asteraceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Balsamorhiza |
---|---|
Linked NCBI taxonomy ID | 121882 |
Linked level | genus |
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 |
---|---|---|---|---|---|---|---|---|
C00004636
![]() |
Tamarixetin
/ 4'-O-Methylquercetin / 3,3',5,7-Tetrahydroxy-4'-methoxyflavone / 3,5,7-Trihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-1-benzopyran-4-one |
CHEMBL226034
|
5 / 6 / 5 | No. 3 | No. 15 |
![]() |
||
C00004640
![]() |
Quercetin 3,4'-dimethyl ether
/ 5,7,3'-Trihydroxy-3,4'-dimethoxyflavone / 5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-3-methoxy-4H-1-benzopyran-4-one |
CHEMBL309263
|
16 / 8 / 2 | No. 3 | No. 15 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P09917 | Arachidonate 5-lipoxygenase | Oxidoreductase | C00004636 | 0 / 0 |
P04798 | Cytochrome P450 1A1 | Cytochrome P450 1A1 | C00004636 | 0 / 0 |
P04792 | Heat shock protein beta-1 | Unclassified protein | C00004636 | 2 / 1 |
Q16678 | Cytochrome P450 1B1 | Cytochrome P450 1B1 | C00004636 | 4 / 4 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00004636 | 0 / 0 |
O14763 | Tumor necrosis factor receptor superfamily member 10B | Unclassified protein | C00004640 | 1 / 0 |
Q13748 | Tubulin alpha-3C/D chain | Structural | C00004640 | 0 / 0 |
P68366 | Tubulin alpha-4A chain | Structural | C00004640 | 0 / 0 |
Q9H4B7 | Tubulin beta-1 chain | Structural | C00004640 | 1 / 0 |
P04350 | Tubulin beta-4A chain | Structural | C00004640 | 2 / 0 |
Q3ZCM7 | Tubulin beta-8 chain | Structural | C00004640 | 0 / 0 |
P07437 | Tubulin beta chain | Structural | C00004640 | 0 / 0 |
Q71U36 | Tubulin alpha-1A chain | Structural | C00004640 | 1 / 1 |
P68371 | Tubulin beta-4B chain | Structural | C00004640 | 0 / 0 |
Q13509 | Tubulin beta-3 chain | Structural | C00004640 | 2 / 1 |
P68363 | Tubulin alpha-1B chain | Unclassified protein | C00004640 | 0 / 0 |
Q13885 | Tubulin beta-2A chain | Structural | C00004640 | 0 / 0 |
Q6PEY2 | Tubulin alpha-3E chain | Unclassified protein | C00004640 | 0 / 0 |
Q9BQE3 | Tubulin alpha-1C chain | Unclassified protein | C00004640 | 0 / 0 |
Q9BUF5 | Tubulin beta-6 chain | Structural | C00004640 | 0 / 0 |
Q9BVA1 | Tubulin beta-2B chain | Structural | C00004640 | 1 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#606595 | Charcot-marie-tooth disease, axonal, type 2f; cmt2f |
P04792
|
#614039 | Cortical dysplasia, complex, with other brain malformations 1; cdcbm1 |
Q13509
|
#128101 | Dystonia 4, torsion, autosomal dominant; dyt4 |
P04350
|
#600638 | Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement; cfeom3a |
Q13509
|
#137750 | Glaucoma 1, open angle, a; glc1a |
Q16678
|
#231300 | Glaucoma 3, primary congenital, a; glc3a |
Q16678
|
#137760 | Glaucoma, primary open angle; poag |
Q16678
|
#612438 | Leukodystrophy, hypomyelinating, 6; hld6 |
P04350
|
#611603 | Lissencephaly 3; lis3 |
Q71U36
|
#613112 | Macrothrombocytopenia, autosomal dominant, tubb1-related |
Q9H4B7
|
#608634 | Neuronopathy, distal hereditary motor, type iib; hmn2b |
P04792
|
#604229 | Peters anomaly |
Q16678
|
#610031 | Polymicrogyria, symmetric or asymmetric; pmgysa |
Q9BVA1
|
#275355 | Squamous cell carcinoma, head and neck; hnscc |
O14763
|
KEGG | name | UniProt |
---|---|---|
H00856 | Distal hereditary motor neuropathies (dHMN) |
P04792
(related)
|
H00838 | Congenital fibrosis of the extraocular muscles (CFEOM) |
Q13509
(related)
|
H00612 | Primary open angle glaucoma |
Q16678
(related)
|
H01075 | Peters anomaly |
Q16678
(related)
|
H01159 | Anterior segment dysgenesis (ASD) |
Q16678
(related)
|
H01203 | Primary congenital glaucoma (PCG) |
Q16678
(related)
|
H00268 | Lissencephaly (LIS) |
Q71U36
(related)
|