Organism name | Gymnopetalum integrifolium |
---|---|
Genus | Gymnopetalum |
Family | Cucurbitaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Gymnopetalum integrifolium |
---|---|
Linked NCBI taxonomy ID | 386178 |
Linked level | species |
Family in NCBI taxonomy | Cucurbitaceae |
---|---|
ID | 3650 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | rosids |
---|---|
ID | 71275 |
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 |
---|---|---|---|---|---|---|---|---|
C00032785
![]() |
Bryoamaride
/ Cucurbitacin l 2-O-beta-D-glucopyranoside |
CHEMBL449483
|
1 / 4 / 2 | No. 315 |
![]() |
|||
C00032622
![]() |
25-O-Acetylbryoamaride
|
No. 315 |
![]() |
|||||
C00032710
![]() |
Aoibaclyin
/ Khekadaengoside G / (-)-Khekadaengoside G |
No. 315 |
![]() |
|||||
C00019308
![]() |
Doursterol
/ Daucosterin / 3-O-beta-D-Glucopyranosyl sitosterol / beta-Sitosterol 3-O-beta-D-glucopyranoside |
CHEMBL197711
CHEMBL506678 CHEMBL2304043 |
C011015
|
5 / 4 / 2 | 0 / 3 | No. 520 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P18031 | Tyrosine-protein phosphatase non-receptor type 1 | Tyr | C00019308 | 0 / 0 |
P06746 | DNA polymerase beta | Enzyme | C00019308 | 0 / 0 |
P08047 | Transcription factor Sp1 | Unclassified protein | C00019308 | 0 / 0 |
P49841 | Glycogen synthase kinase-3 beta | Gsk | C00019308 | 0 / 0 |
P00734 | Prothrombin | S1A | C00019308 | 4 / 2 |
P14679 | Tyrosinase | Oxidoreductase | C00032785 | 4 / 2 |
OMIM | preferred title | UniProt |
---|---|---|
#103470 | Albinism, ocular, with sensorineural deafness |
P14679
|
#203100 | Albinism, oculocutaneous, type ia; oca1a |
P14679
|
#606952 | Albinism, oculocutaneous, type ib; oca1b |
P14679
|
#614390 | Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 |
P00734
|
#613679 | Prothrombin deficiency, congenital |
P00734
|
#601800 | Skin/hair/eye pigmentation, variation in, 3; shep3 |
P14679
|
#601367 | Stroke, ischemic |
P00734
|
#188050 | Thrombophilia due to thrombin defect; thph1 |
P00734
|