class name | count |
---|---|
rosids | 21 |
Embryophyta | 1 |
class name | count |
---|---|
Rutaceae | 21 |
Pelliaceae | 1 |
br08003 Category | # of metabolite |
---|---|
Quinoline alkaloids | 3 |
br08003 Category | KEGG ID | KNApSAcK ID |
---|---|---|
Quinoline alkaloids | C10647 | C00002140 |
Quinoline alkaloids | C10705 | C00002179 |
Quinoline alkaloids | C10711 | C00002181 |
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 |
---|---|---|---|---|---|---|
C00002140
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Balfourodine
|
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||||
C00002179
![]() |
Lemobiline
|
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||||
C00002181
![]() |
Lunacrine
|
CHEMBL2003059
|
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|||
C00025428
![]() |
N-Methylhaplofoline
/ N-Methylkhaplofoline |
CHEMBL24988
|
2 / 13 / 12 |
![]() |
||
C00025442
![]() |
Ravesilone
|
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||||
C00026351
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Ribalinine
/ (-)-Ribalinine / (S)-(-)-Ribalinine |
CHEMBL279711
|
![]() |
|||
C00026352
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Isoplatydesmine
/ 6-Deoxyribaline / (+)-Isoplatydesmine |
CHEMBL21394
|
![]() |
|||
C00026362
![]() |
(+)-Ribaliprenylene
|
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||||
C00026469
![]() |
Oligophyline
|
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||||
C00026497
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Zanthodioline
|
![]() |
||||
C00043796
![]() |
Orixalone D
/ (+)-Orixalone D |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P02545 | Prelamin-A/C | Unclassified protein | C00025428 | 11 / 10 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00025428 | 2 / 2 |
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
|
#119900 | Digital clubbing, isolated congenital |
P15428
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
#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
|
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)
|
H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(related)
|