| Organism name | Encelia virginensis | 
|---|---|
| Genus | Encelia | 
| Family | Asteraceae | 
| Kingdom | Plantae | 
| Linked NCBI taxonomy name | Encelia virginensis | 
|---|---|
| Linked NCBI taxonomy ID | 372415 | 
| Linked level | species | 
| Family in NCBI taxonomy | Asteraceae | 
|---|---|
| ID | 4210 | 
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae | 
|---|---|
| ID | 33090 | 
| Plant class | asterids | 
|---|---|
| ID | 71274 | 
| 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 | 
|---|---|---|---|---|---|---|---|---|
| C00003254   | Encelin | CHEMBL512400 CHEMBL2000615 | C093533 | 1 / 0 / 3 | No. 1231 | No. 38 |   | |
| C00003283   | Farinosin | CHEMBL1439902 | 15 / 16 / 15 | No. 2037 | No. 38 |   | ||
| C00012944   | Virginin / [3S-(3alpha,3abeta,4abeta,8aalpha,9abeta)]-3a,4a,5,8a,9,9a-Hexahydro-3,8a-dimethyl-5-methylenenaphtho[2,3-b]furan-2,6(3H,4H)-dione | No. 2037 | No. 38 |   | 
| accession | description | class description | KNApSAcK metabolite in interactions | # of diseases (OMIM / KEGG) | 
|---|---|---|---|---|
| Q99700 | Ataxin-2 | Unclassified protein | C00003283 | 1 / 1 | 
| P35354 | Prostaglandin G/H synthase 2 | Oxidoreductase | C00003254 | 0 / 3 | 
| P11473 | Vitamin D3 receptor | NR1I1 | C00003283 | 2 / 3 | 
| P42858 | Huntingtin | Unclassified protein | C00003283 | 1 / 1 | 
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00003283 | 2 / 0 | 
| O75496 | Geminin | Unclassified protein | C00003283 | 0 / 0 | 
| P51151 | Ras-related protein Rab-9A | Unclassified protein | C00003283 | 0 / 0 | 
| P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00003283 | 0 / 0 | 
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00003283 | 1 / 2 | 
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00003283 | 0 / 0 | 
| Q9HC16 | DNA dC->dU-editing enzyme APOBEC-3G | Enzyme | C00003283 | 0 / 0 | 
| O15118 | Niemann-Pick C1 protein | Unclassified protein | C00003283 | 1 / 1 | 
| O75030 | Microphthalmia-associated transcription factor | Unclassified protein | C00003283 | 4 / 4 | 
| Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00003283 | 0 / 0 | 
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00003283 | 4 / 3 | 
| Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00003283 | 0 / 0 | 
| OMIM | preferred title | UniProt | 
|---|---|---|
| #103470 | Albinism, ocular, with sensorineural deafness | O75030 | 
| #114500 | Colorectal cancer; crc | P84022 | 
| #600274 | Frontotemporal dementia; ftd | P10636 | 
| #605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay | Q03164 | 
| #143100 | Huntington disease; hd | P42858 | 
| #613795 | Loeys-dietz syndrome, type 3; lds3 | P84022 | 
| #614456 | Melanoma, cutaneous malignant, susceptibility to, 8; cmm8 | O75030 | 
| #607948 | Mycobacterium tuberculosis, susceptibility to | P11473 | 
| #257220 | Niemann-pick disease, type c1; npc1 | O15118 | 
| #260540 | Parkinson-dementia syndrome | P10636 | 
| #172700 | Pick disease of brain | P10636 | 
| #183090 | Spinocerebellar ataxia 2; sca2 | Q99700 | 
| #601104 | Supranuclear palsy, progressive, 1; psnp1 | P10636 | 
| #103500 | Tietz syndrome | O75030 | 
| #277440 | Vitamin d-dependent rickets, type 2a; vddr2a | P11473 | 
| #193510 | Waardenburg syndrome, type 2a; ws2a | O75030 | 
| KEGG | name | UniProt | 
|---|---|---|
| H00136 | Niemann-Pick disease type C (NPC) | O15118
                            (related) | 
| H00038 | Malignant melanoma | O75030
                            (related) O75030 (marker) | 
| H00169 | Ocular albinism | O75030
                            (related) | 
| H00759 | Waardenburg syndrome (WS) | O75030
                            (related) | 
| H01187 | Tietz syndrome | O75030
                            (related) | 
| H00058 | Amyotrophic lateral sclerosis (ALS) | P10636
                            (related) | 
| H00077 | Progressive supranuclear palsy (PSP) | P10636
                            (related) | 
| H00078 | Frontotemporal lobar degeneration (FTLD) | P10636
                            (related) | 
| H00342 | Tuberculosis | P11473
                            (related) | 
| H00784 | Localized autosomal recessive hypotrichosis | P11473
                            (related) | 
| H01143 | Vitamin D-dependent rickets | P11473
                            (related) | 
| H00017 | Esophageal cancer | P35354
                            (related) | 
| H00025 | Penile cancer | P35354
                            (related) | 
| H00046 | Cholangiocarcinoma | P35354
                            (related) | 
| H00059 | Huntington's disease (HD) | P42858
                            (related) | 
| H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) | Q03164
                            (related) Q03164 (marker) | 
| H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) | Q03164
                            (related) | 
| H00063 | Spinocerebellar ataxia (SCA) | Q99700
                            (related) |