class name | count |
---|---|
asterids | 13 |
rosids | 4 |
class name | count |
---|---|
Apiaceae | 13 |
Rutaceae | 4 |
br08003 Category | # of metabolite |
---|---|
Furanocoumarins | 1 |
br08003 Category | KEGG ID | KNApSAcK ID |
---|---|---|
Furanocoumarins | C09282 | C00002490 |
Furanocoumarins | C09282 | C00031473 |
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 |
---|---|---|---|---|---|---|
C00002490
![]() |
Oxypeucedanin
|
CHEMBL510120
CHEMBL1510267 CHEMBL1609439 |
C031535
|
8 / 14 / 11 |
![]() |
|
C00031473
![]() |
(S)-(-)-Oxypeucedanin
|
CHEMBL510120
CHEMBL1510267 CHEMBL1609439 |
8 / 14 / 11 |
![]() |
||
C00037261
![]() |
Heraclenin
|
CHEMBL346814
CHEMBL500034 |
C047845
|
2 / 0 / 0 |
![]() |
|
C00043800
![]() |
Oxyimperatorin
|
CHEMBL346814
CHEMBL500034 |
2 / 0 / 0 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P56817 | Beta-secretase 1 | A1A | C00002490 C00031473 C00037261 C00043800 | 0 / 0 |
O75496 | Geminin | Unclassified protein | C00002490 C00031473 | 0 / 0 |
P10828 | Thyroid hormone receptor beta | NR1A2 | C00002490 C00031473 | 3 / 1 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00002490 C00031473 | 0 / 0 |
P02545 | Prelamin-A/C | Unclassified protein | C00002490 C00031473 | 11 / 10 |
P06746 | DNA polymerase beta | Enzyme | C00002490 C00031473 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00002490 C00031473 | 0 / 0 |
P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00037261 C00043800 | 0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00002490 C00031473 | 0 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#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
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
#248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
#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 |
---|---|---|
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)
|
H00249 | Thyroid hormone resistance syndrome |
P10828
(related)
|