Organism name | Gaillardia pinnatifida |
---|---|
Genus | Gaillardia |
Family | Asteraceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Gaillardia pinnatifida |
---|---|
Linked NCBI taxonomy ID | 373166 |
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 |
---|---|---|---|---|---|---|---|---|
C00021098
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Gaillardilin
|
No. 303 |
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|||||
C00003326
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Mexicanin I
|
CHEMBL338474
CHEMBL354946 CHEMBL486996 CHEMBL1728820 CHEMBL1911137 |
37 / 36 / 29 | No. 495 | No. 38 |
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accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q16637 | Survival motor neuron protein | Unclassified protein | C00003326 | 4 / 1 |
P17861 | X-box-binding protein 1 | Unclassified protein | C00003326 | 1 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00003326 | 1 / 1 |
P49798 | Regulator of G-protein signaling 4 | Unclassified protein | C00003326 | 2 / 0 |
P06746 | DNA polymerase beta | Enzyme | C00003326 | 0 / 0 |
P04062 | Glucosylceramidase | Enzyme | C00003326 | 6 / 4 |
Q9Y5X4 | Photoreceptor-specific nuclear receptor | NR2E3 | C00003326 | 2 / 2 |
P30556 | Type-1 angiotensin II receptor | Angiotensin receptor | C00003326 | 1 / 1 |
P11473 | Vitamin D3 receptor | NR1I1 | C00003326 | 2 / 3 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00003326 | 0 / 0 |
Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00003326 | 0 / 0 |
P42858 | Huntingtin | Unclassified protein | C00003326 | 1 / 1 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00003326 | 2 / 0 |
O75496 | Geminin | Unclassified protein | C00003326 | 0 / 0 |
P51151 | Ras-related protein Rab-9A | Unclassified protein | C00003326 | 0 / 0 |
P38398 | Breast cancer type 1 susceptibility protein | Enzyme | C00003326 | 4 / 2 |
Q9Y2T6 | G-protein coupled receptor 55 | Lysophosphatidylinositol receptor | C00003326 | 0 / 0 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00003326 | 0 / 0 |
Q04206 | Transcription factor p65 | Transcription Factor | C00003326 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00003326 | 1 / 1 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00003326 | 0 / 0 |
Q9HC16 | DNA dC->dU-editing enzyme APOBEC-3G | Enzyme | C00003326 | 0 / 0 |
P06280 | Alpha-galactosidase A | Enzyme | C00003326 | 1 / 1 |
P28482 | Mitogen-activated protein kinase 1 | Erk | C00003326 | 0 / 0 |
Q00987 | E3 ubiquitin-protein ligase Mdm2 | Other nuclear protein | C00003326 | 1 / 5 |
O15118 | Niemann-Pick C1 protein | Unclassified protein | C00003326 | 1 / 1 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00003326 | 0 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00003326 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00003326 | 4 / 3 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00003326 | 0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00003326 | 0 / 0 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00003326 | 1 / 1 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00003326 | 1 / 0 |
Q8IUX4 | DNA dC->dU-editing enzyme APOBEC-3F | Enzyme | C00003326 | 0 / 0 |
Q00653 | Nuclear factor NF-kappa-B p100 subunit | Transcription Factor | C00003326 | 0 / 0 |
P19838 | Nuclear factor NF-kappa-B p105 subunit | Transcription Factor | C00003326 | 0 / 0 |
P01215 | Glycoprotein hormones alpha chain | Unclassified protein | C00003326 | 0 / 3 |
OMIM | preferred title | UniProt |
---|---|---|
#614401 | Accelerated tumor formation, susceptibility to; actfs |
Q00987
|
#114480 | Breast cancer |
P38398
|
#604370 | Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 |
P38398
|
#114500 | Colorectal cancer; crc |
P84022
|
#268100 | Enhanced s-cone syndrome; escs |
Q9Y5X4
|
#301500 | Fabry disease |
P06280
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#608013 | Gaucher disease, perinatal lethal |
P04062
|
#230800 | Gaucher disease, type i |
P04062
|
#230900 | Gaucher disease, type ii |
P04062
|
#231000 | Gaucher disease, type iii |
P04062
|
#231005 | Gaucher disease, type iiic |
P04062
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#143100 | Huntington disease; hd |
P42858
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#612371 | Major affective disorder 7; mafd7 |
P17861
|
#607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
#257220 | Niemann-pick disease, type c1; npc1 |
O15118
|
#167000 | Ovarian cancer |
P38398
|
#614320 | Pancreatic cancer, susceptibility to, 4; pnca4 |
P38398
|
#168600 | Parkinson disease, late-onset; pd |
P04062
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#267430 | Renal tubular dysgenesis; rtd |
P30556
|
#611131 | Retinitis pigmentosa 37; rp37 |
Q9Y5X4
|
#604906 | Schizophrenia 9; sczd9 |
P49798
|
#181500 | Schizophrenia; sczd |
P49798
|
#253300 | Spinal muscular atrophy, type i; sma1 |
Q16637
|
#253550 | Spinal muscular atrophy, type ii; sma2 |
Q16637
|
#253400 | Spinal muscular atrophy, type iii; sma3 |
Q16637
|
#271150 | Spinal muscular atrophy, type iv; sma4 |
Q16637
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | name | UniProt |
---|---|---|
H00136 | Niemann-Pick disease type C (NPC) |
O15118
(related)
|
H00081 | Hashimoto's thyroiditis |
P01215
(marker)
|
H00082 | Graves' disease |
P01215
(marker)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P01215
(marker)
|
H00066 | Lewy body dementia (LBD) |
P04062
(related)
|
H00126 | Gaucher disease |
P04062
(related)
|
H00426 | Defects in the degradation of ganglioside |
P04062
(related)
|
H00810 | Progressive myoclonic epilepsy (PME) |
P04062
(related)
|
H00125 | Fabry disease |
P06280
(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)
|
H00575 | Renal tubular dysgenesis |
P30556
(related)
|
H00027 | Ovarian cancer |
P38398
(related)
|
H00031 | Breast cancer |
P38398
(related)
|
H00059 | Huntington's disease (HD) |
P42858
(related)
|
H00025 | Penile cancer |
Q00987
(related)
|
H00028 | Choriocarcinoma |
Q00987
(related)
|
H00036 | Osteosarcoma |
Q00987
(related)
|
H00037 | Alveolar rhabdomyosarcoma |
Q00987
(related)
|
H00042 | Glioma |
Q00987
(related)
|
H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
Q9NUW8 (related) |
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|
H00527 | Retinitis pigmentosa (RP) |
Q9Y5X4
(related)
|
H00805 | Vitreoretinal degeneration |
Q9Y5X4
(related)
|