class name | count |
---|---|
asterids | 4 |
Magnoliophyta | 3 |
rosids | 3 |
Liliopsida | 1 |
class name | count |
---|---|
Piperaceae | 2 |
Fabaceae | 1 |
Atherospermataceae | 1 |
Apiaceae | 1 |
Boraginaceae | 1 |
Asteraceae | 1 |
Orchidaceae | 1 |
Violaceae | 1 |
Pedaliaceae | 1 |
Begoniaceae | 1 |
br08003 Category | # of metabolite |
---|
br08003 Category | KEGG ID | KNApSAcK ID |
---|
KNApSAcK ID | name | ChEMBL link | CTD link |
# of proteins in
ChEMBL interaction / related OMIM / related KEGG DISEASE |
# of genes in
CTD interaction / related diseases |
figure |
---|---|---|---|---|---|---|
C00002666
![]() |
Piperonal
|
CHEMBL271663
|
C005454
|
3 / 4 / 4 |
![]() |
|
C00002673
![]() |
Sesamol
|
CHEMBL1517998
|
C025583
|
3 / 8 / 8 | 0 / 1 |
![]() |
C00031034
![]() |
Piperonylic acid
/ 3,4-Methylenedioxybenzoic acid |
CHEMBL573781
|
C005455
|
2 / 0 / 0 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P00352 | Retinal dehydrogenase 1 | Enzyme | C00002666 C00031034 | 0 / 0 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00002666 | 3 / 3 |
P28482 | Mitogen-activated protein kinase 1 | Erk | C00031034 | 0 / 0 |
P37231 | Peroxisome proliferator-activated receptor gamma | NR1C3 | C00002673 | 5 / 3 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00002673 | 0 / 1 |
P10275 | Androgen receptor | NR3C4 | C00002673 | 3 / 4 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00002666 | 1 / 1 |
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#300068 | Androgen insensitivity syndrome; ais |
P10275
|
#312300 | Androgen insensitivity, partial; pais |
P10275
|
%606641 | Body mass index; bmi |
P37231
|
#609338 | Carotid intimal medial thickness 1 |
P37231
|
#137800 | Glioma susceptibility 1; glm1 |
P37231
|
#604367 | Lipodystrophy, familial partial, type 3; fpld3 |
P37231
|
#300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
#300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
#601665 | Obesity |
P37231
|
#313200 | Spinal and bulbar muscular atrophy, x-linked 1; smax1 |
P10275
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
KEGG | name | UniProt |
---|---|---|
H00036 | Osteosarcoma |
P08684
(marker)
|
H00024 | Prostate cancer |
P10275
(related)
|
H00062 | Spinal and bulbar muscular atrophy (SBMA) |
P10275
(related)
|
H00608 | 46,XY disorders of sex development (Disorders in androgen synthesis or action) |
P10275
(related)
|
H00609 | 46,XY disorders of sex development (Other) |
P10275
(related)
|
H00032 | Thyroid cancer |
P37231
(related)
|
H00409 | Type II diabetes mellitus |
P37231
(related)
|
H00420 | Familial partial lipodystrophy (FPL) |
P37231
(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)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q9NUW8
(related)
|