Organism name | Juniperus lucayana |
---|---|
Genus | Juniperus |
Family | Cupressaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Juniperus barbadensis var. lucayana |
---|---|
Linked NCBI taxonomy ID | 487037 |
Linked level | varietas |
Family in NCBI taxonomy | Cupressaceae |
---|---|
ID | 3367 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | Spermatophyta |
---|---|
ID | 58024 |
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 |
---|---|---|---|---|---|---|---|---|
C00007234
![]() |
Katuranin
/ (+)-Aromadendrin / (+)-Dihydrokaempferol / (2R,3R)-2,3-Dihydro-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one |
CHEMBL9323
CHEMBL1933859 |
C080220
|
4 / 3 / 3 | No. 42 | No. 14 |
![]() |
|
C00034371
![]() |
15-Hydroxyallocedrol
|
No. 161 | No. 38 |
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||||
C00003112
![]() |
Cedrol
/ (+)-Cedrol / alpha-Cedrol |
CHEMBL1592444
CHEMBL1974890 |
C078669
|
5 / 14 / 11 | No. 161 | No. 38 |
![]() |
|
C00021966
![]() |
Allocedrol
/ allo-Cedrol |
No. 161 | No. 38 |
![]() |
||||
C00029679
![]() |
alpha-Bisabolol
|
CHEMBL519167
CHEMBL491186 CHEMBL477832 CHEMBL1096927 CHEMBL1171719 CHEMBL1561544 CHEMBL2104360 |
C004497
|
8 / 4 / 13 | No. 541 | No. 38 |
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|
C00034367
![]() |
12-Hydroxywiddrol
/ (+)-12-Hydroxywiddrol |
No. 3284 |
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|||||
C00021963
![]() |
Widdrol
|
C078670
|
No. 3284 |
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||||
C00034391
![]() |
3-Hydroxypseudowiddran-6(7)-en-4-ol
/ (+)-3-Hydroxypseudowiddran-6(7)-en-4-ol |
No. 3284 |
![]() |
|||||
C00034455
![]() |
beta-Chamigrenic acid
|
No. 3683 |
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accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P28482 | Mitogen-activated protein kinase 1 | Erk | C00003112 C00029679 | 0 / 0 |
P16050 | Arachidonate 15-lipoxygenase | Enzyme | C00003112 C00029679 | 0 / 0 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00007234 | 0 / 0 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00003112 | 0 / 0 |
P36888 | Receptor-type tyrosine-protein kinase FLT3 | Pdgfr | C00007234 | 1 / 1 |
O75496 | Geminin | Unclassified protein | C00007234 | 0 / 0 |
P40763 | Signal transducer and activator of transcription 3 | Transcription Factor | C00029679 | 1 / 2 |
P10828 | Thyroid hormone receptor beta | NR1A2 | C00003112 | 3 / 1 |
O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00029679 | 0 / 0 |
P11511 | Cytochrome P450 19A1 | Cytochrome P450 19A1 | C00007234 | 2 / 2 |
P35354 | Prostaglandin G/H synthase 2 | Oxidoreductase | C00029679 | 0 / 3 |
P02545 | Prelamin-A/C | Unclassified protein | C00003112 | 11 / 10 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00029679 | 0 / 1 |
O00255 | Menin | Unclassified protein | C00029679 | 2 / 5 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00029679 | 1 / 2 |
OMIM | preferred title | UniProt |
---|---|---|
#613546 | Aromatase deficiency |
P11511
|
#139300 | Aromatase excess syndrome; aexs |
P11511
|
#115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
#212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
#605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#147060 | Hyper-ige recurrent infection syndrome, autosomal dominant |
P40763
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#601626 | Leukemia, acute myeloid; aml |
P36888
|
#151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
#248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
#613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
#159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#188570 | Thyroid hormone resistance, generalized, autosomal dominant; grth |
P10828
|
#274300 | Thyroid hormone resistance, generalized, autosomal recessive; grth |
P10828
|
#145650 | Thyroid hormone resistance, selective pituitary; prth |
P10828
|
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)
|
H00264 | Charcot-Marie-Tooth disease (CMT) |
P02545
(related)
|
H00294 | Dilated cardiomyopathy (DCM) |
P02545
(related)
|
H00420 | Familial partial lipodystrophy (FPL) |
P02545
(related)
|
H00563 | Emery-Dreifuss muscular dystrophy |
P02545
(related)
|
H00590 | Congenital muscular dystrophies (CMD/MDC) |
P02545
(related)
|
H00593 | Limb-girdle muscular dystrophy (LGMD) |
P02545
(related)
|
H00601 | Hutchinson-Gilford progeria syndrome |
P02545
(related)
|
H00663 | Restrictive dermopathy |
P02545
(related)
|
H00665 | Mandibuloacral dysplasia |
P02545
(related)
|
H01216 | Left ventricular noncompaction (LVNC) |
P02545
(related)
|
H00036 | Osteosarcoma |
P08684
(marker)
|
H00249 | Thyroid hormone resistance syndrome |
P10828
(related)
|
H00599 | 46,XX disorders of sex development (Disorders related to androgen excess) |
P11511
(related)
|
H00794 | Aromatase excess syndrome |
P11511
(related)
|
H00017 | Esophageal cancer |
P35354
(related)
|
H00025 | Penile cancer |
P35354
(related)
|
H00046 | Cholangiocarcinoma |
P35354
(related)
|
H00003 | Acute myeloid leukemia (AML) |
P36888
(related)
|
H00016 | Oral cancer |
P40763
(related)
|
H00107 | Other well-defined immunodeficiency syndromes |
P40763
(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)
|