Organism name | Cerastium arvense |
---|---|
Genus | Cerastium |
Family | Caryophyllaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Cerastium arvense |
---|---|
Linked NCBI taxonomy ID | 271558 |
Linked level | species |
Family in NCBI taxonomy | Caryophyllaceae |
---|---|
ID | 3568 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | eudicotyledons |
---|---|
ID | 71240 |
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 |
---|---|---|---|---|---|---|---|---|
C00006388
![]() |
Cerarvensin 7-O-glucoside
|
No. 1 | No. 15 |
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||||
C00006386
![]() |
Isomollupentin 2''-O-glucoside
|
No. 1 | No. 15 |
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||||
C00006166
![]() |
6-C-beta-D-Xylopyranosyl-8-C-alpha-L-arabinopyranosylapigenin
|
No. 1 | No. 15 |
![]() |
||||
C00006183
![]() |
Isocorymboside
|
CHEMBL1537012
|
7 / 2 / 2 | No. 1 | No. 15 |
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||
C00006235
![]() |
6-C-Glucopyranosyl-8-C-galactopyranosylapigenin
|
CHEMBL1442950
|
6 / 14 / 8 | No. 1 | No. 15 |
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||
C00006378
![]() |
Isovitexin 2''-O-xyloside
|
No. 1 | No. 15 |
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||||
C00006385
![]() |
Isomollupentin 4'-O-glucoside
|
No. 1 | No. 15 |
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||||
C00006384
![]() |
Isomollupentin 7-O-glucoside
|
No. 1 | No. 15 |
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||||
C00006306
![]() |
Isomollupentin 7-O-glucoside-2''-O-arabinoside
|
No. 5 | No. 15 |
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||||
C00006305
![]() |
Isomollupentin 7-O-glucoside-2''-O-xyloside
|
No. 5 | No. 15 |
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||||
C00006322
![]() |
Isovitexin 7,2''-di-O-glucoside
|
No. 5 | No. 15 |
![]() |
||||
C00006332
![]() |
Isovitexin 4'-O-glucoside 2''-O-(E)-ferulate
|
No. 7 | No. 15 |
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||||
C00006331
![]() |
Isoorientin 4'-O-glucoside 2''-O-(E)-ferulate
|
No. 7 | No. 15 |
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||||
C00006079
![]() |
Isomollupentin
/ 6-C-Arabinosylapigenin / 6-alpha-L-Arabinopyranosyl-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one |
No. 22 | No. 15 |
![]() |
||||
C00006078
![]() |
Cerarvensin
/ 5,7-Dihydroxy-2-(4-hydroxyphenyl)-6-beta-D-xylopyranosyl-4H-1-benzopyran-4-one |
No. 22 | No. 15 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00006183 C00006235 | 1 / 1 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00006183 C00006235 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00006183 | 1 / 1 |
P39748 | Flap endonuclease 1 | Enzyme | C00006183 | 0 / 0 |
P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00006235 | 7 / 3 |
P06746 | DNA polymerase beta | Enzyme | C00006183 | 0 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00006183 | 0 / 0 |
P04062 | Glucosylceramidase | Enzyme | C00006235 | 6 / 4 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00006183 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00006235 | 0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00006235 | 0 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
#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
|
#232300 | Glycogen storage disease ii |
P10253
|
#174800 | Mccune-albright syndrome; mas |
P63092
|
#166350 | Osseous heteroplasia, progressive; poh |
P63092
|
#168600 | Parkinson disease, late-onset; pd |
P04062
|
#102200 | Pituitary adenoma, growth hormone-secreting |
P63092
|
#103580 | Pseudohypoparathyroidism, type ia; php1a |
P63092
|
#603233 | Pseudohypoparathyroidism, type ib; php1b |
P63092
|
#612462 | Pseudohypoparathyroidism, type ic; php1c |
P63092
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
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)
|
H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|