Species

KNApSAcK Entry

Organism name Citrus aurantium ssp.bergamia
Genus Citrus
Family Rutaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Citrus
Linked NCBI taxonomy ID 2706
Linked level genus

Family

Family in NCBI taxonomy Rutaceae
ID 23513

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (2)

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
C00010301 External link 512 Coriandrol
/ (S)-Linalool
/ S-(+)-Linalool
/ (+)-S-Linalool
/ (S)-3,7-Dimethyl-1,6-octadien-3-ol
CHEMBL25306
CHEMBL235672
6 / 8 / 2 No. 958 No. 34
C00003048 External link 512 Linalyl acetate
/ Linaloyl acetate
CHEMBL502773
C074463
1 / 0 / 1 No. 4126 No. 34

Human Protein / Gene in interactions

7 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P22310 UDP-glucuronosyltransferase 1-4 Enzyme C00010301 3 / 0
P10828 Thyroid hormone receptor beta NR1A2 C00010301 3 / 1
P83916 Chromobox protein homolog 1 Unclassified protein C00010301 0 / 0
P04150 Glucocorticoid receptor NR3C1 C00003048 0 / 1
Q9Y4X1 UDP-glucuronosyltransferase 2A1 Enzyme C00010301 0 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme C00010301 0 / 0
P22309 UDP-glucuronosyltransferase 1-1 Enzyme C00010301 5 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (8)

OMIM preferred title UniProt
#601816 Bilirubin, serum level of, quantitative trait locus 1; biliqtl1 P22309
#218800 Crigler-najjar syndrome, type i P22309
P22310
#606785 Crigler-najjar syndrome, type ii P22309
P22310
#143500 Gilbert syndrome P22309
P22310
#237900 Hyperbilirubinemia, transient familial neonatal; hblrtfn P22309
#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 (3)

KEGG name UniProt
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00208 Hyperbilirubinemia P22309 (related)