Organism name | Salvia compressa |
---|---|
Genus | Salvia |
Family | Labiatae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Salvia |
---|---|
Linked NCBI taxonomy ID | 21880 |
Linked level | genus |
Family in NCBI taxonomy | Lamiaceae |
---|---|
ID | 4136 |
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 |
---|---|---|---|---|---|---|---|---|
C00004632
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Quercetin 3-methyl ether
/ Quercetin 3-O-methyl ether |
CHEMBL163316
|
32 / 21 / 21 | No. 3 | No. 15 |
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accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00004632 | 0 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00004632 | 1 / 1 |
P06746 | DNA polymerase beta | Enzyme | C00004632 | 0 / 0 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00004632 | 1 / 1 |
P07550 | Beta-2 adrenergic receptor | Adrenergic receptor | C00004632 | 0 / 1 |
P04792 | Heat shock protein beta-1 | Unclassified protein | C00004632 | 2 / 1 |
P54132 | Bloom syndrome protein | Enzyme | C00004632 | 1 / 2 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00004632 | 1 / 0 |
P39748 | Flap endonuclease 1 | Enzyme | C00004632 | 0 / 0 |
P42858 | Huntingtin | Unclassified protein | C00004632 | 1 / 1 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00004632 | 2 / 0 |
O75496 | Geminin | Unclassified protein | C00004632 | 0 / 0 |
P15121 | Aldose reductase | Enzyme | C00004632 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00004632 | 1 / 1 |
Q9HC16 | DNA dC->dU-editing enzyme APOBEC-3G | Enzyme | C00004632 | 0 / 0 |
P11021 | 78 kDa glucose-regulated protein | Unclassified protein | C00004632 | 0 / 0 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00004632 | 3 / 3 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00004632 | 0 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00004632 | 0 / 0 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00004632 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00004632 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00004632 | 4 / 3 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00004632 | 0 / 0 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00004632 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00004632 | 0 / 0 |
P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00004632 | 0 / 0 |
Q8IUX4 | DNA dC->dU-editing enzyme APOBEC-3F | Enzyme | C00004632 | 0 / 0 |
O00255 | Menin | Unclassified protein | C00004632 | 2 / 5 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00004632 | 1 / 2 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00004632 | 0 / 0 |
Q9H0H5 | Rac GTPase-activating protein 1 | Unclassified protein | C00004632 | 0 / 0 |
Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00004632 | 2 / 1 |
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#210900 | Bloom syndrome; blm |
P54132
|
#606595 | Charcot-marie-tooth disease, axonal, type 2f; cmt2f |
P04792
|
#114500 | Colorectal cancer; crc |
P84022
Q14191 |
#600274 | Frontotemporal dementia; ftd |
P10636
|
#232300 | Glycogen storage disease ii |
P10253
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#143100 | Huntington disease; hd |
P42858
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
#300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#608634 | Neuronopathy, distal hereditary motor, type iib; hmn2b |
P04792
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#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)
|
H00856 | Distal hereditary motor neuropathies (dHMN) |
P04792
(related)
|
H00079 | Asthma |
P07550
(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)
|
H00059 | Huntington's disease (HD) |
P42858
(related)
|
H00094 | DNA repair defects |
P54132
(related)
|
H00296 | Defects in RecQ helicases |
P54132
(related)
Q14191 (related) |
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q03164
(related)
Q03164 (marker) |
H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) |
Q03164
(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)
|