| Organism name | Aphomia sociella |
|---|---|
| Genus | Aphomia |
| Family | Pyralidae |
| Kingdom | Animalia |
| Linked NCBI taxonomy name | Aphomia sociella |
|---|---|
| Linked NCBI taxonomy ID | 688398 |
| Linked level | species |
| Family in NCBI taxonomy | Pyralidae |
|---|---|
| ID | 7135 |
| Kingdom (Superkingdom) in NCBI taxonomy | Metazoa |
|---|---|
| ID | 33208 |
| Plant class | |
|---|---|
| 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 |
KCF-S
cluster |
phytochemical
cluster |
figure |
|---|---|---|---|---|---|---|---|---|
|
C00047334
|
Phytone
/ (+)-Phytone |
No. 641 | No. 38 |
|
||||
|
C00002663
|
2-Phenylethanol
/ Phenethyl alcohol / Phenylethyl alcohol / beta-Phenethyl alcohol |
CHEMBL448500
|
D010626
|
2 / 1 / 1 | No. 885 |
|
||
|
C00000550
|
Mellein
/ Ochracin / (R)-(-)-Mellein |
CHEMBL226090
CHEMBL499303 |
2 / 2 / 0 | No. 1274 |
|
|||
|
C00000358
|
n-Hexanol
|
CHEMBL14085
|
C036260
|
3 / 6 / 3 | No. 3722 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P16473 | Thyrotropin receptor | Glycohormone receptor | C00000358 | 3 / 2 |
| P10828 | Thyroid hormone receptor beta | NR1A2 | C00000358 | 3 / 1 |
| O75496 | Geminin | Unclassified protein | C00002663 | 0 / 0 |
| Q9UGP5 | DNA polymerase lambda | Enzyme | C00000550 | 0 / 0 |
| Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00000358 | 0 / 0 |
| P28340 | DNA polymerase delta catalytic subunit | Transferase | C00000550 | 2 / 0 |
| Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00002663 | 1 / 1 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #612591 | Colorectal cancer, susceptibility to, 10; crcs10 |
P28340
|
| #603373 | Hyperthyroidism, familial gestational |
P16473
|
| #609152 | Hyperthyroidism, nonautoimmune |
P16473
|
| #275200 | Hypothyroidism, congenital, nongoitrous, 1; chng1 |
P16473
|
| #615381 | Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome; mdpl |
P28340
|
| #607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
| #188570 | Thyroid hormone resistance, generalized, autosomal dominant; grth |
P10828
|
| #274300 | Thyroid hormone resistance, generalized, autosomal recessive; grth |
P10828
|
| #145650 | Thyroid hormone resistance, selective pituitary; prth |
P10828
|