Organism name | Sargassum fallax |
---|---|
Genus | Sargassum |
Family | Sargassaceae |
Kingdom | Chromalveolata |
Linked NCBI taxonomy name | Sargassum fallax |
---|---|
Linked NCBI taxonomy ID | 129343 |
Linked level | species |
Family in NCBI taxonomy | Sargassaceae |
---|---|
ID | 3014 |
Kingdom (Superkingdom) in NCBI taxonomy | Eukaryota |
---|---|
ID | 2759 |
Plant class | |
---|---|
ID |
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 |
---|---|---|---|---|---|---|---|---|
C00048390
![]() |
Fallaquinone
|
No. 661 |
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|||||
C00031302
![]() |
Sargaquinoic acid
|
No. 661 |
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|||||
C00048388
![]() |
Fallachromenoic acid
/ (-)-Fallachromenoic acid |
No. 2359 |
![]() |
|||||
C00031300
![]() |
Sargachromenol
|
CHEMBL1668777
CHEMBL1668778 |
7 / 7 / 10 | No. 2359 |
![]() |
|||
C00048389
![]() |
Fallahydroquinone
|
No. 3586 |
![]() |
|||||
C00031301
![]() |
Sargahydroquinoic acid
|
CHEMBL261063
|
No. 3586 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P10276 | Retinoic acid receptor alpha | NR1B1 | C00031300 | 1 / 2 |
P04150 | Glucocorticoid receptor | NR3C1 | C00031300 | 0 / 1 |
P06401 | Progesterone receptor | NR3C3 | C00031300 | 0 / 1 |
Q96RI1 | Bile acid receptor | NR1H4 | C00031300 | 0 / 0 |
P03372 | Estrogen receptor | NR3A1 | C00031300 | 1 / 1 |
P08235 | Mineralocorticoid receptor | NR3C2 | C00031300 | 2 / 2 |
P10275 | Androgen receptor | NR3C4 | C00031300 | 3 / 4 |
OMIM | preferred title | UniProt |
---|---|---|
#612376 | Acute promyelocytic leukemia; apl |
P10276
|
#300068 | Androgen insensitivity syndrome; ais |
P10275
|
#312300 | Androgen insensitivity, partial; pais |
P10275
|
#615363 | Estrogen resistance; estrr |
P03372
|
#605115 | Hypertension, early-onset, autosomal dominant, with severe exacerbation in pregnancy |
P08235
|
#177735 | Pseudohypoaldosteronism, type i, autosomal dominant; pha1a |
P08235
|
#313200 | Spinal and bulbar muscular atrophy, x-linked 1; smax1 |
P10275
|
KEGG | name | UniProt |
---|---|---|
H00026 | Endometrial Cancer |
P03372
(marker)
P06401 (marker) |
H00599 | 46,XX disorders of sex development (Disorders related to androgen excess) |
P04150
(related)
|
H00243 | Hyperkalemic distal renal tubular acidosis (RTA type 4) |
P08235
(related)
|
H00603 | Hypertension exacerbated in pregnancy |
P08235
(related)
|
H00024 | Prostate cancer |
P10275
(related)
|
H00062 | Spinal and bulbar muscular atrophy (SBMA) |
P10275
(related)
|
H00608 | 46,XY disorders of sex development (Disorders in androgen synthesis or action) |
P10275
(related)
|
H00609 | 46,XY disorders of sex development (Other) |
P10275
(related)
|
H00003 | Acute myeloid leukemia (AML) |
P10276
(related)
P10276 (marker) |
H00516 | Isolated orofacial clefts |
P10276
(related)
|