class name | count |
---|---|
rosids | 8 |
class name | count |
---|---|
Rutaceae | 7 |
Moraceae | 1 |
br08003 Category | # of metabolite |
---|---|
Furanocoumarins | 1 |
br08003 Category | KEGG ID | KNApSAcK ID |
---|---|---|
Furanocoumarins | C09165 | C00002456 |
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 |
---|---|---|---|---|---|---|
C00002456
![]() |
Chalepensin
|
CHEMBL1333931
|
C020740
|
7 / 8 / 6 |
![]() |
|
C00019781
![]() |
Anisocoumarin A
|
![]() |
||||
C00037165
![]() |
Furopinnarin
|
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P04062 | Glucosylceramidase | Enzyme | C00002456 | 6 / 4 |
P42858 | Huntingtin | Unclassified protein | C00002456 | 1 / 1 |
O75496 | Geminin | Unclassified protein | C00002456 | 0 / 0 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00002456 | 0 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00002456 | 0 / 0 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00002456 | 0 / 0 |
Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00002456 | 1 / 1 |
OMIM | preferred title | UniProt |
---|---|---|
#612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
#608013 | Gaucher disease, perinatal lethal |
P04062
|
#230800 | Gaucher disease, type i |
P04062
|
#230900 | Gaucher disease, type ii |
P04062
|
#231000 | Gaucher disease, type iii |
P04062
|
#231005 | Gaucher disease, type iiic |
P04062
|
#143100 | Huntington disease; hd |
P42858
|
#168600 | Parkinson disease, late-onset; pd |
P04062
|
KEGG | name | UniProt |
---|---|---|
H00066 | Lewy body dementia (LBD) |
P04062
(related)
|
H00126 | Gaucher disease |
P04062
(related)
|
H00426 | Defects in the degradation of ganglioside |
P04062
(related)
|
H00810 | Progressive myoclonic epilepsy (PME) |
P04062
(related)
|
H00059 | Huntington's disease (HD) |
P42858
(related)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
Q13148
(related)
|