Species

KNApSAcK Entry

Organism name Coscinium fenestratum (Gaertn.)Colebr.
Genus Coscinium
Family Menispermaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Coscinium fenestratum
Linked NCBI taxonomy ID 483232
Linked level species

Family

Family in NCBI taxonomy Menispermaceae
ID 3455

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class eudicotyledons
ID 71240

Metabolite list (3)

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
C00026154 External link 512 Thalifendine
CHEMBL1187148
C477156
No. 155 No. 4
C00026111 External link 512 Berberrubine
/ 9-Berberoline
CHEMBL203135
CHEMBL2160119
5 / 10 / 6 No. 155 No. 4
C00025998 External link 512 Oxypalmatine
No. 439

Human Protein / Gene in interactions

5 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q99700 Ataxin-2 Unclassified protein C00026111 1 / 1
Q09428 ATP-binding cassette sub-family C member 8 K C00026111 5 / 3
Q14654 ATP-sensitive inward rectifier potassium channel 11 K C00026111 3 / 4
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00026111 0 / 0
Q14191 Werner syndrome ATP-dependent helicase Enzyme C00026111 2 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (10)

OMIM preferred title UniProt
#114500 Colorectal cancer; crc Q14191
#606176 Diabetes mellitus, permanent neonatal; pndm Q09428
Q14654
#610374 Diabetes mellitus, transient neonatal, 2 Q09428
#610582 Diabetes mellitus, transient neonatal, 3 Q14654
#256450 Hyperinsulinemic hypoglycemia, familial, 1; hhf1 Q09428
#601820 Hyperinsulinemic hypoglycemia, familial, 2; hhf2 Q14654
#602485 Hyperinsulinemic hypoglycemia, familial, 3; hhf3 Q09428
#240800 Hypoglycemia, leucine-induced; lih Q09428
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#277700 Werner syndrome; wrn Q14191

KEGG DISEASE (6)

KEGG name UniProt
H00512 Permanent neonatal diabetes mellitus (PNDM) Q09428 (related)
Q14654 (related)
H00513 Transient neonatal diabetes mellitus (TNDM) Q09428 (related)
Q14654 (related)
H01267 Familial hyperinsulinemic hypoglycemia (HHF) Q09428 (related)
Q14654 (related)
H00296 Defects in RecQ helicases Q14191 (related)
H00409 Type II diabetes mellitus Q14654 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)