PCIDB

Cymbopogon flexuosus

Family in NCBI taxonomy	Poaceae
ID	4479

Kingdom (Superkingdom) in NCBI taxonomy	Viridiplantae
ID	33090

Plant class	Liliopsida
ID	4447

KNApSAcK ID	name	ChEMBL link	# of proteins in ChEMBL interaction / related OMIM / related KEGG DISEASE	KCF-S cluster	phytochemical cluster
C00003672	Sitosterol / beta-sitosterl / (-)-beta-Sitosterol / Stigmast-5-en-3beta-ol	CHEMBL221542 CHEMBL1398443 CHEMBL1875388	17 / 19 / 12	No. 53	No. 11
C00012812	Isointermedeol	CHEMBL481844 CHEMBL505457		No. 398	No. 38
C00003036	Neral / Citral Z	CHEMBL1080997	6 / 7 / 9	No. 1575	No. 34
C00003035	Geranial / (E)-alpha-Citral	CHEMBL1080997	6 / 7 / 9	No. 1575	No. 34

accession	description	class description	KNApSAcK metabolite in interactions	# of diseases (OMIM / KEGG)
Q01196	Runt-related transcription factor 1	Unclassified protein	C00003035 C00003036	1 / 4
Q13951	Core-binding factor subunit beta	Unclassified protein	C00003035 C00003036	0 / 1
P10275	Androgen receptor	NR3C4	C00003035 C00003036	3 / 4
P10828	Thyroid hormone receptor beta	NR1A2	C00003035 C00003036	3 / 1
P00352	Retinal dehydrogenase 1	Enzyme	C00003035 C00003036	0 / 0
O00519	Fatty-acid amide hydrolase 1	Enzyme	C00003035 C00003036	0 / 0
P16473	Thyrotropin receptor	Glycohormone receptor	C00003672	3 / 2
P08183	Multidrug resistance protein 1	drug	C00003672	1 / 0
P11712	Cytochrome P450 2C9	Cytochrome P450 2C9	C00003672	0 / 1
P08047	Transcription factor Sp1	Unclassified protein	C00003672	0 / 0
P49841	Glycogen synthase kinase-3 beta	Gsk	C00003672	0 / 0
P06746	DNA polymerase beta	Enzyme	C00003672	0 / 0
P00734	Prothrombin	S1A	C00003672	4 / 2
P14679	Tyrosinase	Oxidoreductase	C00003672	4 / 2
P05177	Cytochrome P450 1A2	Cytochrome P450 1A2	C00003672	0 / 0
P03372	Estrogen receptor	NR3A1	C00003672	1 / 1
P33261	Cytochrome P450 2C19	Cytochrome P450 2C19	C00003672	1 / 1
P08684	Cytochrome P450 3A4	Cytochrome P450 3A4	C00003672	0 / 1
P49798	Regulator of G-protein signaling 4	Unclassified protein	C00003672	2 / 0
P80365	Corticosteroid 11-beta-dehydrogenase isozyme 2	Enzyme	C00003672	1 / 1
Q9NUW8	Tyrosyl-DNA phosphodiesterase 1	Enzyme	C00003672	1 / 1
P18031	Tyrosine-protein phosphatase non-receptor type 1	Tyr	C00003672	0 / 0
P10635	Cytochrome P450 2D6	Cytochrome P450 2D6	C00003672	1 / 0

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
#218030	Apparent mineralocorticoid excess; ame	P80365
#609535	Drug metabolism, poor, cyp2c19-related	P33261
#608902	Drug metabolism, poor, cyp2d6-related	P10635
#615363	Estrogen resistance; estrr	P03372
#603373	Hyperthyroidism, familial gestational	P16473
#609152	Hyperthyroidism, nonautoimmune	P16473
#275200	Hypothyroidism, congenital, nongoitrous, 1; chng1	P16473
#612244	Inflammatory bowel disease 13; ibd13	P08183
#601399	Platelet disorder, familial, with associated myeloid malignancy	Q01196
#614390	Pregnancy loss, recurrent, susceptibility to, 2; rprgl2	P00734
#613679	Prothrombin deficiency, congenital	P00734
#604906	Schizophrenia 9; sczd9	P49798
#181500	Schizophrenia; sczd	P49798
#601800	Skin/hair/eye pigmentation, variation in, 3; shep3	P14679
#313200	Spinal and bulbar muscular atrophy, x-linked 1; smax1	P10275
#607250	Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1	Q9NUW8
#601367	Stroke, ischemic	P00734
#188050	Thrombophilia due to thrombin defect; thph1	P00734
#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	name	UniProt
H00223	Inherited thrombophilia	P00734 (related)
H01254	Congenital prothrombin deficiency	P00734 (related)
H00026	Endometrial Cancer	P03372 (marker)
H00036	Osteosarcoma	P08684 (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)
H01205	Coumarin resistance	P11712 (related)
H00168	Oculocutaneous albinism (OCA)	P14679 (related)
H00038	Malignant melanoma	P14679 (marker)
H00250	Congenital nongoitrous hypothyroidism (CHNG)	P16473 (related)
H01269	Congenital hyperthyroidism	P16473 (related)
H01171	Poor drug metabolism (PM)	P33261 (related)
H00259	Apparent mineralocorticoid excess syndrome	P80365 (related)
H00001	Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia)	Q01196 (related) Q01196 (marker)
H00003	Acute myeloid leukemia (AML)	Q01196 (related) Q01196 (marker) Q13951 (marker)
H00004	Chronic myeloid leukemia (CML)	Q01196 (related)
H00978	Thrombocytopenia (THC)	Q01196 (related)
H00063	Spinocerebellar ataxia (SCA)	Q9NUW8 (related)