Organism name | Gentiana spp. |
---|---|
Genus | Gentiana |
Family | Gentianaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Gentiana |
---|---|
Linked NCBI taxonomy ID | 21496 |
Linked level | genus |
Family in NCBI taxonomy | Gentianaceae |
---|---|
ID | 21472 |
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 |
---|---|---|---|---|---|---|---|---|
C00006205
![]() |
Isoorientin 4'-O-glucoside
|
No. 1 | No. 15 |
![]() |
||||
C00006393
![]() |
Isosaponarin
|
CHEMBL1643081
|
No. 1 | No. 15 |
![]() |
|||
C00014782
![]() |
Delphinidin 3,3'-di-glucoside-5-(6-p-coumarylglucoside)
|
No. 7 | No. 15 |
![]() |
||||
C00014781
![]() |
Delphinidin 3,3'-di-glucoside-5-(6-caffeoylglucoside)
|
No. 7 | No. 15 |
![]() |
||||
C00014820
![]() |
Delphinidin 3-glucoside-5-(6-(E)-p-coumaroylglucoside)
|
No. 7 | No. 15 |
![]() |
||||
C00001055
![]() |
Isoorientin
/ Homoorientin / Lespecapitioside / Luteolin 6-C-beta-D-glucopyranoside / 2-(3,4-Dihydroxyphenyl)-6-beta-D-glucopyranosyl-5,7-dihydroxy-4H-1-benzopyran-4-one |
CHEMBL239559
CHEMBL1302308 |
C057912
|
23 / 14 / 17 | 0 / 1 | No. 22 | No. 15 |
![]() |
C00001058
![]() |
Isoscoparin
/ Isoorientin 3'-methyl ether |
No. 22 | No. 15 |
![]() |
||||
C00014819
![]() |
Delphinidin 3-glucoside-5-(6-caffeoylglucoside)-3'-(6-(E)-p-coumaroylglucoside)
|
No. 62 | No. 15 |
![]() |
||||
C00002648
![]() |
Gentisic acid
/ 2,5-Dihydroxybenzoic acid |
CHEMBL1461
|
C010925
|
15 / 6 / 8 | 2 / 1 | No. 817 | No. 81 |
![]() |
C00001135
![]() |
Gentianose
|
CHEMBL175500
CHEMBL603717 |
No. 1765 |
![]() |
||||
C00001977
![]() |
Gentianine
|
C060402
|
No. 3439 |
![]() |
||||
C00001978
![]() |
Gentiflavine
|
No. 8677 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q9UNA4 | DNA polymerase iota | Enzyme | C00001055 C00002648 | 0 / 0 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00002648 | 0 / 0 |
P09917 | Arachidonate 5-lipoxygenase | Oxidoreductase | C00002648 | 0 / 0 |
P06746 | DNA polymerase beta | Enzyme | C00001055 | 0 / 0 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00001055 | 1 / 1 |
P43166 | Carbonic anhydrase 7 | Lyase | C00002648 | 0 / 0 |
P22894 | Neutrophil collagenase | M10A | C00002648 | 0 / 0 |
P14780 | Matrix metalloproteinase-9 | M10A | C00002648 | 2 / 2 |
Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00001055 | 0 / 0 |
P00918 | Carbonic anhydrase 2 | Lyase | C00002648 | 1 / 2 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00001055 | 1 / 0 |
Q9ULX7 | Carbonic anhydrase 14 | Lyase | C00002648 | 0 / 0 |
O43570 | Carbonic anhydrase 12 | Lyase | C00002648 | 1 / 2 |
P39748 | Flap endonuclease 1 | Enzyme | C00001055 | 0 / 0 |
P00915 | Carbonic anhydrase 1 | Lyase | C00002648 | 0 / 0 |
P03956 | Interstitial collagenase | M10A | C00002648 | 0 / 1 |
Q9Y253 | DNA polymerase eta | Enzyme | C00001055 | 1 / 1 |
Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | C00001055 | 0 / 0 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00001055 | 0 / 0 |
Q16790 | Carbonic anhydrase 9 | Lyase | C00002648 | 0 / 1 |
P08253 | 72 kDa type IV collagenase | M10A | C00002648 | 1 / 3 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00001055 | 0 / 0 |
P18031 | Tyrosine-protein phosphatase non-receptor type 1 | Tyr | C00002648 | 0 / 0 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00001055 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00001055 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00001055 | 4 / 3 |
P08254 | Stromelysin-1 | M10A | C00002648 | 1 / 0 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00001055 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00001055 | 0 / 0 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00001055 | 1 / 1 |
O00255 | Menin | Unclassified protein | C00001055 | 2 / 5 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00001055 | 1 / 2 |
Q13951 | Core-binding factor subunit beta | Unclassified protein | C00001055 | 0 / 1 |
Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00001055 | 1 / 4 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00001055 | 0 / 0 |
Q9H0H5 | Rac GTPase-activating protein 1 | Unclassified protein | C00001055 | 0 / 0 |
Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00001055 | 2 / 1 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
2539 | G6PD, G6PD1 | glucose-6-phosphate dehydrogenase (EC:1.1.1.49) |
C00002648
|
6817 | SULT1A1, HAST1/HAST2, P-PST, PST, ST1A1, ST1A3, STP, STP1, TSPST1 | sulfotransferase family, cytosolic, 1A, phenol-preferring, member 1 (EC:2.8.2.1) |
C00002648
|
OMIM | preferred title | UniProt |
---|---|---|
#114500 | Colorectal cancer; crc |
Q14191
|
#614466 | Coronary heart disease, susceptibility to, 6; chds6 |
P08254
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#232300 | Glycogen storage disease ii |
P10253
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#143860 | Hyperchlorhidrosis, isolated |
O43570
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#603932 | Intervertebral disc disease; idd |
P14780
|
#613073 | Metaphyseal anadysplasia 2; mandp2 |
P14780
|
#259600 | Multicentric osteolysis, nodulosis, and arthropathy; mona |
P08253
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#259730 | Osteopetrosis, autosomal recessive 3; optb3 |
P00918
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#601399 | Platelet disorder, familial, with associated myeloid malignancy |
Q01196
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#277700 | Werner syndrome; wrn |
Q14191
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | name | UniProt |
---|---|---|
H00033 | Adrenal carcinoma |
O00255
(related)
|
H00034 | Carcinoid |
O00255
(related)
|
H00045 | Malignant islet cell carcinoma |
O00255
(related)
|
H00246 | Primary hyperparathyroidism |
O00255
(related)
|
H01102 | Pituitary adenomas |
O00255
(related)
|
H01302 | Hyperchlorhidrosis isolated (HCHLH) |
O43570
(related)
|
H00021 | Renal cell carcinoma |
O43570
(marker)
Q16790 (marker) |
H00241 | Combined proximal and distal renal tubular acidosis (RTA type 3) |
P00918
(related)
|
H00436 | Osteopetrosis |
P00918
(related)
|
H00028 | Choriocarcinoma |
P03956
(related)
P08253 (related) |
H00025 | Penile cancer |
P08253
(related)
P14780 (related) |
H00472 | Torg-Winchester syndrome |
P08253
(related)
|
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)
|
H00479 | Metaphyseal dysplasias |
P14780
(related)
|
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q01196
(related)
Q01196 (marker) Q03164 (related) Q03164 (marker) |
H00003 | Acute myeloid leukemia (AML) |
Q01196
(related)
Q01196 (marker) Q13951 (marker) |
H00004 | Chronic myeloid leukemia (CML) |
Q01196
(related)
|
H00978 | Thrombocytopenia (THC) |
Q01196
(related)
|
H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) |
Q03164
(related)
|
H00296 | Defects in RecQ helicases |
Q14191
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q9NUW8
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|