Organism name | Eucalyptus sieberi |
---|---|
Genus | Eucalyptus |
Family | Myrtaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Eucalyptus sieberi |
---|---|
Linked NCBI taxonomy ID | 87684 |
Linked level | species |
Family in NCBI taxonomy | Myrtaceae |
---|---|
ID | 3931 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | rosids |
---|---|
ID | 71275 |
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 |
---|---|---|---|---|---|---|---|---|
C00008145
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Pinocembrin 5,7-dimethyl ether
|
CHEMBL107131
CHEMBL1253912 |
9 / 14 / 11 | No. 25 | No. 14 |
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accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P49798 | Regulator of G-protein signaling 4 | Unclassified protein | C00008145 | 2 / 0 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00008145 | 0 / 0 |
P28482 | Mitogen-activated protein kinase 1 | Erk | C00008145 | 0 / 0 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00008145 | 3 / 3 |
Q9UNQ0 | ATP-binding cassette sub-family G member 2 | ATP binding cassette | C00008145 | 2 / 0 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00008145 | 2 / 2 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00008145 | 0 / 1 |
O14746 | Telomerase reverse transcriptase | Enzyme | C00008145 | 5 / 5 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00008145 | 0 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#609135 | Aplastic anemia |
O14746
|
#614490 | Blood group, junior system; jr |
Q9UNQ0
|
#119900 | Digital clubbing, isolated congenital |
P15428
|
#613989 | Dyskeratosis congenita, autosomal dominant, 2; dkca2 |
O14746
|
#259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
#615134 | Melanoma, cutaneous malignant, susceptibility to, 9; cmm9 |
O14746
|
#300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
#300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
#614742 | Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1; pfbmft1 |
O14746
|
#178500 | Pulmonary fibrosis, idiopathic; ipf |
O14746
|
#604906 | Schizophrenia 9; sczd9 |
P49798
|
#181500 | Schizophrenia; sczd |
P49798
|
#138900 | Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 |
Q9UNQ0
|
KEGG | name | UniProt |
---|---|---|
H00764 | Cri du chat syndrome |
O14746
(related)
|
H01132 | Aplastic anemia (AA) |
O14746
(related)
|
H01299 | Idiopathic pulmonary fibrosis |
O14746
(related)
|
H00022 | Bladder cancer |
O14746
(marker)
|
H00024 | Prostate cancer |
O14746
(marker)
|
H00036 | Osteosarcoma |
P08684
(marker)
|
H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(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)
|