PCIDB

Beta spp.

Family in NCBI taxonomy	Amaranthaceae
ID	3563

Kingdom (Superkingdom) in NCBI taxonomy	Viridiplantae
ID	33090

Plant class	eudicotyledons
ID	71240

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
C00002727	Coniferin / Coniferoside	CHEMBL459056	C016316	2 / 0 / 0		No. 678	No. 6
C00002683	Vanillin	CHEMBL13883		18 / 8 / 9		No. 1003

accession	description	class description	KNApSAcK metabolite in interactions	# of diseases (OMIM / KEGG)
Q9HAW8	UDP-glucuronosyltransferase 1-10	Enzyme	C00002683	0 / 0
P78527	DNA-dependent protein kinase catalytic subunit	Atypical serine/threonine protein kinase PIKK subfamily	C00002683	0 / 0
P19793	Retinoic acid receptor RXR-alpha	NR2B1	C00002683	0 / 0
P51649	Succinate-semialdehyde dehydrogenase, mitochondrial	Oxidoreductase	C00002683	1 / 1
P34969	5-hydroxytryptamine receptor 7	Serotonin receptor	C00002683	0 / 0
Q9HAW7	UDP-glucuronosyltransferase 1-7	Enzyme	C00002683	0 / 0
P23219	Prostaglandin G/H synthase 1	Oxidoreductase	C00002727	0 / 0
P00352	Retinal dehydrogenase 1	Enzyme	C00002683	0 / 0
P39748	Flap endonuclease 1	Enzyme	C00002727	0 / 0
O60656	UDP-glucuronosyltransferase 1-9	Enzyme	C00002683	0 / 0
O00519	Fatty-acid amide hydrolase 1	Enzyme	C00002683	0 / 0
P80404	4-aminobutyrate aminotransferase, mitochondrial	Transferase	C00002683	1 / 1
Q96RI1	Bile acid receptor	NR1H4	C00002683	0 / 0
P15428	15-hydroxyprostaglandin dehydrogenase [NAD(+)]	Enzyme	C00002683	2 / 2
Q9Y4X1	UDP-glucuronosyltransferase 2A1	Enzyme	C00002683	0 / 0
P19224	UDP-glucuronosyltransferase 1-6	Enzyme	C00002683	0 / 0
Q16236	Nuclear factor erythroid 2-related factor 2	Unclassified protein	C00002683	0 / 0
P10275	Androgen receptor	NR3C4	C00002683	3 / 4
Q9NUW8	Tyrosyl-DNA phosphodiesterase 1	Enzyme	C00002683	1 / 1
O94925	Glutaminase kidney isoform, mitochondrial	Enzyme	C00002683	0 / 0

OMIM	preferred title	UniProt
#300068	Androgen insensitivity syndrome; ais	P10275
#312300	Androgen insensitivity, partial; pais	P10275
#119900	Digital clubbing, isolated congenital	P15428
#613163	Gaba-transaminase deficiency	P80404
#259100	Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1	P15428
#313200	Spinal and bulbar muscular atrophy, x-linked 1; smax1	P10275
#607250	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1	Q9NUW8
#271980	Succinic semialdehyde dehydrogenase deficiency; ssadhd	P51649

KEGG	name	UniProt
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)
H00457	Primary hypertrophic osteoarthropathy (PHO)	P15428 (related)
H01246	Isolated congenital nail clubbing (ICNC)	P15428 (related)
H00835	Succinic semialdehyde dehydrogenase (SSADH) deficiency	P51649 (related)
H01257	GABA-transaminase deficiency	P80404 (related)
H00063	Spinocerebellar ataxia (SCA)	Q9NUW8 (related)