Organism name | Primula officinalis |
---|---|
Genus | Primula |
Family | Primulaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Primula |
---|---|
Linked NCBI taxonomy ID | 49647 |
Linked level | genus |
Family in NCBI taxonomy | Primulaceae |
---|---|
ID | 4335 |
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 |
---|---|---|---|---|---|---|---|---|
C00005538
![]() |
Isorhamnetin 3-robinobioside
/ Isorhamnetin 3-O-robinobioside |
CHEMBL84174
CHEMBL258394 CHEMBL1711509 CHEMBL2165403 |
7 / 1 / 2 | No. 1 | No. 15 |
![]() |
||
C00005160
![]() |
Kaempferol 3-robinobioside
|
CHEMBL431610
CHEMBL79790 CHEMBL255020 CHEMBL501550 CHEMBL498879 CHEMBL1419228 CHEMBL1875691 |
22 / 10 / 12 | No. 1 | No. 15 |
![]() |
||
C00005401
![]() |
Quercetin 3-robinoside
/ Quercetin 3-O-robinoside / Quercetin 3-O-robinobioside / Quercetin 3-O-rhamnosyl-(1->6)-galactoside |
CHEMBL32579
CHEMBL310754 CHEMBL182108 CHEMBL226335 CHEMBL502782 CHEMBL1436093 CHEMBL1532989 |
25 / 18 / 16 | No. 1 | No. 15 |
![]() |
||
C00005411
![]() |
Quercetin 3-gentiobioside
|
CHEMBL1097317
|
C088177
|
No. 1 | No. 15 |
![]() |
||
C00005715
![]() |
Limocitrin 3-glucoside
/ Limocitrin 3-O-beta-glucopyranoside / Limocitrin 3-O-beta-D-glucopyranoside |
No. 2 | No. 15 |
![]() |
||||
C00005783
![]() |
Limocitrol 3-glucoside
|
No. 2 | No. 15 |
![]() |
||||
C00004792
![]() |
Limocitrol
|
No. 3 | No. 15 |
![]() |
||||
C00005444
![]() |
Quercetin 3-(2Gal-rhamnosyl-robinobioside)
|
CHEMBL444468
|
No. 5 | No. 15 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P06746 | DNA polymerase beta | Enzyme | C00005160 C00005401 | 0 / 0 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00005160 C00005401 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00005160 C00005401 | 0 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00005160 C00005538 | 0 / 0 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00005401 C00005538 | 0 / 1 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00005160 C00005401 | 1 / 1 |
P03372 | Estrogen receptor | NR3A1 | C00005401 C00005538 | 1 / 1 |
P47989 | Xanthine dehydrogenase/oxidase | Oxidoreductase | C00005160 C00005401 | 1 / 1 |
O75496 | Geminin | Unclassified protein | C00005160 C00005538 | 0 / 0 |
P07237 | Protein disulfide-isomerase | Enzyme | C00005160 C00005538 | 0 / 0 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00005160 C00005401 | 1 / 0 |
P14679 | Tyrosinase | Oxidoreductase | C00005401 | 4 / 2 |
P11473 | Vitamin D3 receptor | NR1I1 | C00005160 | 2 / 3 |
P39748 | Flap endonuclease 1 | Enzyme | C00005160 | 0 / 0 |
P18825 | Alpha-2C adrenergic receptor | Adrenergic receptor | C00005401 | 0 / 0 |
P08913 | Alpha-2A adrenergic receptor | Adrenergic receptor | C00005401 | 0 / 0 |
P27487 | Dipeptidyl peptidase 4 | S9B | C00005401 | 0 / 1 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00005538 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00005160 | 1 / 1 |
Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | C00005160 | 0 / 0 |
O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00005401 | 0 / 0 |
P11388 | DNA topoisomerase 2-alpha | Isomerase | C00005401 | 0 / 0 |
P06276 | Cholinesterase | Hydrolase | C00005401 | 0 / 0 |
P28482 | Mitogen-activated protein kinase 1 | Erk | C00005401 | 0 / 0 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00005401 | 3 / 3 |
Q9UNQ0 | ATP-binding cassette sub-family G member 2 | ATP binding cassette | C00005401 | 2 / 0 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00005538 | 0 / 0 |
Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00005160 | 0 / 0 |
P22303 | Acetylcholinesterase | Hydrolase | C00005401 | 1 / 0 |
P33527 | Multidrug resistance-associated protein 1 | drugs | C00005401 | 0 / 0 |
P35354 | Prostaglandin G/H synthase 2 | Oxidoreductase | C00005401 | 0 / 3 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00005160 | 0 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00005160 | 1 / 1 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00005401 | 4 / 3 |
P48147 | Prolyl endopeptidase | S9A | C00005401 | 0 / 0 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00005160 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00005401 | 0 / 0 |
P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00005160 | 0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00005401 | 0 / 0 |
Q13951 | Core-binding factor subunit beta | Unclassified protein | C00005160 | 0 / 1 |
Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00005160 | 1 / 4 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00005160 | 0 / 0 |
Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00005160 | 2 / 1 |
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#103470 | Albinism, ocular, with sensorineural deafness |
P14679
|
#203100 | Albinism, oculocutaneous, type ia; oca1a |
P14679
|
#606952 | Albinism, oculocutaneous, type ib; oca1b |
P14679
|
#614490 | Blood group, junior system; jr |
Q9UNQ0
|
#114500 | Colorectal cancer; crc |
Q14191
|
#615363 | Estrogen resistance; estrr |
P03372
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#232300 | Glycogen storage disease ii |
P10253
|
#300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
#300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
#607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#601399 | Platelet disorder, familial, with associated myeloid malignancy |
Q01196
|
#601800 | Skin/hair/eye pigmentation, variation in, 3; shep3 |
P14679
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#138900 | Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 |
Q9UNQ0
|
#277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
#277700 | Werner syndrome; wrn |
Q14191
|
#278300 | Xanthinuria, type i |
P47989
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
#112100 | Yt blood group antigen |
P22303
|
KEGG | name | UniProt |
---|---|---|
H00026 | Endometrial Cancer |
P03372
(marker)
|
H00036 | Osteosarcoma |
P08684
(marker)
|
H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00342 | Tuberculosis |
P11473
(related)
|
H00784 | Localized autosomal recessive hypotrichosis |
P11473
(related)
|
H01143 | Vitamin D-dependent rickets |
P11473
(related)
|
H00168 | Oculocutaneous albinism (OCA) |
P14679
(related)
|
H00038 | Malignant melanoma |
P14679
(marker)
|
H00032 | Thyroid cancer |
P27487
(marker)
|
H00017 | Esophageal cancer |
P35354
(related)
|
H00025 | Penile cancer |
P35354
(related)
|
H00046 | Cholangiocarcinoma |
P35354
(related)
|
H00192 | Xanthinuria |
P47989
(related)
|
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q01196
(related)
Q01196 (marker) |
H00003 | Acute myeloid leukemia (AML) |
Q01196
(related)
Q01196 (marker) Q13951 (marker) |
H00004 | Chronic myeloid leukemia (CML) |
Q01196
(related)
|
H00978 | Thrombocytopenia (THC) |
Q01196
(related)
|
H00296 | Defects in RecQ helicases |
Q14191
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|
H00480 | Non-syndromic X-linked mental retardation |
Q99714
(related)
|
H00658 | Syndromic X-linked mental retardation |
Q99714
(related)
|
H00925 | 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency |
Q99714
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|