| class name | count |
|---|---|
| rosids | 1 |
| class name | count |
|---|---|
| Brassicaceae | 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 |
|---|---|---|---|---|---|---|
|
C00007414
|
2-Ethylhexanoic acid
|
CHEMBL1162485
CHEMBL1162486 CHEMBL1162487 |
C040668
|
4 / 4 / 6 | 1 / 6 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P00918 | Carbonic anhydrase 2 | Lyase | C00007414 | 1 / 2 |
| P00915 | Carbonic anhydrase 1 | Lyase | C00007414 | 0 / 0 |
| P28482 | Mitogen-activated protein kinase 1 | Erk | C00007414 | 0 / 0 |
| P10275 | Androgen receptor | NR3C4 | C00007414 | 3 / 4 |
| gene | gene name | gene description | KNApSAcK metabolite in interactions |
|---|---|---|---|
| 5465 | PPARA, NR1C1, PPAR, PPARalpha, hPPAR | peroxisome proliferator-activated receptor alpha |
C00007414
|
| OMIM | preferred title | UniProt |
|---|---|---|
| #300068 | Androgen insensitivity syndrome; ais |
P10275
|
| #312300 | Androgen insensitivity, partial; pais |
P10275
|
| #259730 | Osteopetrosis, autosomal recessive 3; optb3 |
P00918
|
| #313200 | Spinal and bulbar muscular atrophy, x-linked 1; smax1 |
P10275
|
| KEGG | name | UniProt |
|---|---|---|
| H00241 | Combined proximal and distal renal tubular acidosis (RTA type 3) |
P00918
(related)
|
| H00436 | Osteopetrosis |
P00918
(related)
|
| 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)
|
| MESH or OMIM | name |
KNApSAcK
metabolite |
|---|---|---|
| D000014 | Abnormalities, Drug-Induced |
C00007414
|
| D000015 | Abnormalities, Multiple |
C00007414
|
| D004677 | Encephalocele |
C00007414
|
| D005317 | Fetal Growth Retardation |
C00007414
|
| D010490 | Pericardial Effusion |
C00007414
|
| D049188 | Prenatal Injuries |
C00007414
|