PCIDB

Orthodon carvoriferum

Species

KNApSAcK Entry

Organism name Orthodon carvoriferum
Genus Orthodon
Family Cyprinidae
Kingdom Animalia

NCBI taxonomy

Entry

Linked NCBI taxonomy name Orthodon
Linked NCBI taxonomy ID 71766
Linked level genus

Family

Family in NCBI taxonomy Cyprinidae
ID 7953

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Metazoa
ID 33208

Plant class

Plant class
ID

Metabolite list (1)

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
C00010891 External link 512 (S)-(+)-Carvone
CHEMBL15676
CHEMBL501949
8 / 9 / 9 No. 1740 No. 35

Human Protein / Gene in interactions

8 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P49798 Regulator of G-protein signaling 4 Unclassified protein C00010891 2 / 0
P10828 Thyroid hormone receptor beta NR1A2 C00010891 3 / 1
P00352 Retinal dehydrogenase 1 Enzyme C00010891 0 / 0
P51449 Nuclear receptor ROR-gamma Nuclear hormone receptor subfamily 1 group F member 3 C00010891 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00010891 0 / 0
O00255 Menin Unclassified protein C00010891 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00010891 1 / 2
Q13148 TAR DNA-binding protein 43 Unclassified protein C00010891 1 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (9)

OMIM preferred title UniProt
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#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 (9)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00058 Amyotrophic lateral sclerosis (ALS) Q13148 (related)