PCIDB

Pelea madagascariensis

Species

KNApSAcK Entry

Organism name Pelea madagascariensis
Genus Pelea
Family Rutaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Pelea
Linked NCBI taxonomy ID 59551
Linked level genus

Family

Family in NCBI taxonomy Bovidae
ID 9895

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
C00002636 External link 512 Anisaldehyde
/ p-Anisaldehyde
CHEMBL161598
C024896
11 / 18 / 13 1 / 0 No. 1003

Human Protein / Gene in interactions

11 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10828 Thyroid hormone receptor beta NR1A2 C00002636 3 / 1
P51649 Succinate-semialdehyde dehydrogenase, mitochondrial Oxidoreductase C00002636 1 / 1
P00352 Retinal dehydrogenase 1 Enzyme C00002636 0 / 0
P11509 Cytochrome P450 2A6 Cytochrome P450 2A6 C00002636 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00002636 0 / 0
P14679 Tyrosinase Oxidoreductase C00002636 4 / 2
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00002636 5 / 3
P80404 4-aminobutyrate aminotransferase, mitochondrial Transferase C00002636 1 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00002636 0 / 0
P03372 Estrogen receptor NR3A1 C00002636 1 / 1
P10275 Androgen receptor NR3C4 C00002636 3 / 4

1 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
8989 TRPA1, ANKTM1, FEPS transient receptor potential cation channel, subfamily A, member 1 C00002636

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (18)

OMIM preferred title UniProt
#103470 Albinism, ocular, with sensorineural deafness P14679
#203100 Albinism, oculocutaneous, type ia; oca1a P14679
#606952 Albinism, oculocutaneous, type ib; oca1b P14679
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
%606641 Body mass index; bmi P37231
#609338 Carotid intimal medial thickness 1 P37231
#615363 Estrogen resistance; estrr P03372
#613163 Gaba-transaminase deficiency P80404
#137800 Glioma susceptibility 1; glm1 P37231
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#601665 Obesity P37231
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#271980 Succinic semialdehyde dehydrogenase deficiency; ssadhd P51649
#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 (13)

KEGG name UniProt
H00026 Endometrial Cancer P03372 (marker)
H00024 Prostate cancer P10275 (related)
H00062 Spinal and bulbar muscular atrophy (SBMA) P10275 (related)
H00608 46,XY disorders of sex development (Disorders in androgen synthesis or action) P10275 (related)
H00609 46,XY disorders of sex development (Other) P10275 (related)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00038 Malignant melanoma P14679 (marker)
H00032 Thyroid cancer P37231 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00420 Familial partial lipodystrophy (FPL) P37231 (related)
H00835 Succinic semialdehyde dehydrogenase (SSADH) deficiency P51649 (related)
H01257 GABA-transaminase deficiency P80404 (related)