PCIDB

Primula denticulata

Species

KNApSAcK Entry

Organism name Primula denticulata
Genus Primula
Family Primulaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Primula denticulata
Linked NCBI taxonomy ID 175055
Linked level species

Family

Family in NCBI taxonomy Primulaceae
ID 4335

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

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
C00003812 External link 512 5-Hydroxy-6,2'-dimethoxyflavone
No. 35 No. 15
C00006918 External link 512 2,2'-Dihydroxychalcone
CHEMBL150755
CHEMBL1700548
14 / 18 / 10 No. 92 No. 13

Human Protein / Gene in interactions

14 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q99700 Ataxin-2 Unclassified protein C00006918 1 / 1
P37840 Alpha-synuclein Unclassified protein C00006918 4 / 2
P11473 Vitamin D3 receptor NR1I1 C00006918 2 / 3
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00006918 2 / 0
O75496 Geminin Unclassified protein C00006918 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00006918 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00006918 7 / 3
Q9Y253 DNA polymerase eta Enzyme C00006918 1 / 1
P83916 Chromobox protein homolog 1 Unclassified protein C00006918 0 / 0
P11021 78 kDa glucose-regulated protein Unclassified protein C00006918 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00006918 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00006918 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00006918 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00006918 1 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (18)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#114500 Colorectal cancer; crc P84022
#127750 Dementia, lewy body; dlb P37840
#137800 Glioma susceptibility 1; glm1 O75874
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#174800 Mccune-albright syndrome; mas P63092
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#166350 Osseous heteroplasia, progressive; poh P63092
#168601 Parkinson disease 1, autosomal dominant; park1 P37840
#605543 Parkinson disease 4, autosomal dominant; park4 P37840
#168600 Parkinson disease, late-onset; pd P37840
#102200 Pituitary adenoma, growth hormone-secreting P63092
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (10)

KEGG name UniProt
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H00057 Parkinson's disease (PD) P37840 (related)
H00066 Lewy body dementia (LBD) P37840 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)