Organism name | Orthosiphon labiatus |
---|---|
Genus | Orthosiphon |
Family | Labiatae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Orthosiphon |
---|---|
Linked NCBI taxonomy ID | 204150 |
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 |
---|---|---|---|---|---|---|---|---|
C00038087
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(+)-trans-Ozic acid
|
CHEMBL498097
CHEMBL1488779 CHEMBL1731589 |
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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 | C00038087 | 0 / 0 |
P06746 | DNA polymerase beta | Enzyme | C00038087 | 0 / 0 |
P39748 | Flap endonuclease 1 | Enzyme | C00038087 | 0 / 0 |
P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00038087 | 7 / 3 |
Q9Y253 | DNA polymerase eta | Enzyme | C00038087 | 1 / 1 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00038087 | 0 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00038087 | 0 / 0 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00038087 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00038087 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00038087 | 4 / 3 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00038087 | 0 / 0 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00038087 | 0 / 0 |
Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00038087 | 2 / 1 |
OMIM | preferred title | UniProt |
---|---|---|
#219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
#114500 | Colorectal cancer; crc |
Q14191
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#174800 | Mccune-albright syndrome; mas |
P63092
|
#166350 | Osseous heteroplasia, progressive; poh |
P63092
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#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
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#277700 | Werner syndrome; wrn |
Q14191
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | name | UniProt |
---|---|---|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|
H00296 | Defects in RecQ helicases |
Q14191
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|