class name | count |
---|
class name | count |
---|---|
Aplysiidae | 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 |
---|---|---|---|---|---|---|
C00034591
![]() |
Malevamide D
|
CHEMBL453182
|
![]() |
|||
C00044726
![]() |
Dolastatin 10
/ (-)-Dolastatin 10 |
CHEMBL106850
CHEMBL322390 CHEMBL108116 CHEMBL104543 CHEMBL432610 CHEMBL325114 CHEMBL321425 CHEMBL319657 CHEMBL321271 CHEMBL321910 CHEMBL321911 CHEMBL320475 CHEMBL431233 CHEMBL1713020 CHEMBL1980788 CHEMBL2111674 CHEMBL2111675 CHEMBL2111676 CHEMBL2111677 CHEMBL2111678 |
C064570
|
6 / 11 / 6 |
![]() |
|
C00046443
![]() |
Symplostatin 1
|
CHEMBL501233
CHEMBL1224776 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q99700 | Ataxin-2 | Unclassified protein | C00044726 | 1 / 1 |
O75496 | Geminin | Unclassified protein | C00044726 | 0 / 0 |
P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00044726 | 7 / 3 |
P51843 | Nuclear receptor subfamily 0 group B member 1 | Nuclear hormone receptor subfamily 0 group B member 1 | C00044726 | 2 / 2 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00044726 | 0 / 0 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00044726 | 1 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#300018 | 46,xy sex reversal 2; srxy2 |
P51843
|
#219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
#300200 | Adrenal hypoplasia, congenital; ahc |
P51843
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#174800 | Mccune-albright syndrome; mas |
P63092
|
#166350 | Osseous heteroplasia, progressive; poh |
P63092
|
#102200 | Pituitary adenoma, growth hormone-secreting |
P63092
|
#103580 | Pseudohypoparathyroidism, type ia; php1a |
P63092
|
#603233 | Pseudohypoparathyroidism, type ib; php1b |
P63092
|
#612462 | Pseudohypoparathyroidism, type ic; php1c |
P63092
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
KEGG | name | UniProt |
---|---|---|
H00552 | Glycerol kinase deficiency (GKD) |
P51843
(related)
|
H00607 | 46,XY disorders of sex development (Disorders of gonadal development) |
P51843
(related)
|
H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|