Species

KNApSAcK Entry

Organism name Aphomia sociella
Genus Aphomia
Family Pyralidae
Kingdom Animalia

NCBI taxonomy

Entry

Linked NCBI taxonomy name Aphomia sociella
Linked NCBI taxonomy ID 688398
Linked level species

Family

Family in NCBI taxonomy Pyralidae
ID 7135

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Metazoa
ID 33208

Plant class

Plant class
ID

Metabolite list (4)

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 External link 512 Phytone
/ (+)-Phytone
No. 641 No. 38
C00002663 External link 512 2-Phenylethanol
/ Phenethyl alcohol
/ Phenylethyl alcohol
/ beta-Phenethyl alcohol
CHEMBL448500
D010626
2 / 1 / 1 No. 885
C00000550 External link 512 Mellein
/ Ochracin
/ (R)-(-)-Mellein
CHEMBL226090
CHEMBL499303
2 / 2 / 0 No. 1274
C00000358 External link 512 n-Hexanol
CHEMBL14085
C036260
3 / 6 / 3 No. 3722

Human Protein / Gene in interactions

7 ChEMBL Protein in interactions

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

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (9)

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

KEGG DISEASE (4)

KEGG name UniProt
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)