class name | count |
---|---|
rosids | 4 |
asterids | 3 |
Spermatophyta | 2 |
eudicotyledons | 1 |
class name | count |
---|---|
Solanaceae | 2 |
Alariaceae | 1 |
Brassicaceae | 1 |
Pinaceae | 1 |
Fabaceae | 1 |
Amaranthaceae | 1 |
Begoniaceae | 1 |
Cucurbitaceae | 1 |
Chalinidae | 1 |
Asteraceae | 1 |
Ephedraceae | 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 |
---|---|---|---|---|---|---|
C00000113
![]() |
Indole-3-carboxylic acid
|
CHEMBL387527
|
C012382
|
1 / 3 / 4 |
![]() |
|
C00001540
![]() |
6-Hydroxykynurenic acid
|
![]() |
||||
C00026494
![]() |
Transtorine
|
CHEMBL299155
|
23 / 12 / 17 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00026494 | 1 / 0 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00026494 | 0 / 0 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00026494 | 1 / 1 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00026494 | 0 / 1 |
Q9HC97 | G-protein coupled receptor 35 | Kynurenic acid receptor | C00026494 | 0 / 0 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00026494 | 0 / 0 |
O75496 | Geminin | Unclassified protein | C00026494 | 0 / 0 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00026494 | 1 / 2 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00026494 | 0 / 0 |
P06280 | Alpha-galactosidase A | Enzyme | C00026494 | 1 / 1 |
P08138 | Tumor necrosis factor receptor superfamily member 16 | Membrane receptor | C00026494 | 0 / 0 |
P28482 | Mitogen-activated protein kinase 1 | Erk | C00026494 | 0 / 0 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00026494 | 0 / 0 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00026494 | 3 / 3 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00026494 | 2 / 2 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00026494 | 1 / 1 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00026494 | 0 / 1 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00026494 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00026494 | 0 / 0 |
P10275 | Androgen receptor | NR3C4 | C00000113 | 3 / 4 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00026494 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00026494 | 0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00026494 | 0 / 0 |
O00255 | Menin | Unclassified protein | C00026494 | 2 / 5 |
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#300068 | Androgen insensitivity syndrome; ais |
P10275
|
#312300 | Androgen insensitivity, partial; pais |
P10275
|
#119900 | Digital clubbing, isolated congenital |
P15428
|
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#301500 | Fabry disease |
P06280
|
#232300 | Glycogen storage disease ii |
P10253
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
#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
|
#313200 | Spinal and bulbar muscular atrophy, x-linked 1; smax1 |
P10275
|
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)
|
H00125 | Fabry disease |
P06280
(related)
|
H00036 | Osteosarcoma |
P08684
(marker)
|
H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
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)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(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)
|
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)
|