class name | count |
---|---|
rosids | 10 |
asterids | 2 |
Euphyllophyta | 1 |
class name | count |
---|---|
Rutaceae | 8 |
Solanaceae | 2 |
Brassicaceae | 2 |
Salviniaceae | 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 |
---|---|---|---|---|---|---|
C00007546
![]() |
Methylbenzoate
|
CHEMBL16435
|
4 / 6 / 6 |
![]() |
||
C00034054
![]() |
Methyl benzoate
|
CHEMBL16435
|
C044605
|
4 / 6 / 6 |
![]() |
|
C00034600
![]() |
Methyl anthranilate
|
CHEMBL1493986
|
C038892
|
3 / 3 / 3 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00007546 C00034054 C00034600 | 0 / 0 |
P16473 | Thyrotropin receptor | Glycohormone receptor | C00007546 C00034054 | 3 / 2 |
P10145 | Interleukin-8 | Secreted protein | C00007546 C00034054 | 0 / 0 |
P10275 | Androgen receptor | NR3C4 | C00007546 C00034054 | 3 / 4 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00034600 | 0 / 0 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00034600 | 3 / 3 |
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#300068 | Androgen insensitivity syndrome; ais |
P10275
|
#312300 | Androgen insensitivity, partial; pais |
P10275
|
#603373 | Hyperthyroidism, familial gestational |
P16473
|
#609152 | Hyperthyroidism, nonautoimmune |
P16473
|
#275200 | Hypothyroidism, congenital, nongoitrous, 1; chng1 |
P16473
|
#300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
#300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
#313200 | Spinal and bulbar muscular atrophy, x-linked 1; smax1 |
P10275
|
KEGG | name | UniProt |
---|---|---|
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)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P16473
(related)
|
H01269 | Congenital hyperthyroidism |
P16473
(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)
|