Organism name | Schisandra rubriflora |
---|---|
Genus | Schisandra |
Family | Schisandraceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Schisandra rubriflora |
---|---|
Linked NCBI taxonomy ID | 124791 |
Linked level | species |
Family in NCBI taxonomy | Schisandraceae |
---|---|
ID | 16733 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | Magnoliophyta |
---|---|
ID | 3398 |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00007215 C00041224 C00041495 C00041563 | 0 / 0 |
O75496 | Geminin | Unclassified protein | C00007215 C00041224 C00041495 C00041563 | 0 / 0 |
P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00007215 C00041563 | 7 / 3 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00007215 C00041224 | 0 / 0 |
Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00007215 C00041224 | 1 / 1 |
Q99700 | Ataxin-2 | Unclassified protein | C00007215 C00041563 | 1 / 1 |
Q13315 | Serine-protein kinase ATM | Atypical serine/threonine protein kinase PIKK subfamily | C00041495 C00041563 | 1 / 4 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00007215 C00041224 | 2 / 0 |
P00918 | Carbonic anhydrase 2 | Lyase | C00007215 | 1 / 2 |
P17405 | Sphingomyelin phosphodiesterase | Enzyme | C00007215 | 2 / 2 |
Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00041563 | 0 / 0 |
P37840 | Alpha-synuclein | Unclassified protein | C00007215 | 4 / 2 |
Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00007215 | 0 / 0 |
P00915 | Carbonic anhydrase 1 | Lyase | C00007215 | 0 / 0 |
P35218 | Carbonic anhydrase 5A, mitochondrial | Lyase | C00007215 | 0 / 0 |
Q9Y2D0 | Carbonic anhydrase 5B, mitochondrial | Lyase | C00007215 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00041224 | 1 / 1 |
P04150 | Glucocorticoid receptor | NR3C1 | C00007215 | 0 / 1 |
P06746 | DNA polymerase beta | Enzyme | C00041224 | 0 / 0 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00007215 | 0 / 0 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00041563 | 1 / 1 |
P33527 | Multidrug resistance-associated protein 1 | drugs | C00041495 | 0 / 0 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
1576 | CYP3A4, CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4, HLP, NF-25, P450C3, P450PCN1 | cytochrome P450, family 3, subfamily A, polypeptide 4 (EC:1.14.13.67 1.14.13.97 1.14.13.32 1.14.13.157) |
C00041495
|
8856 | NR1I2, BXR, ONR1, PAR, PAR1, PAR2, PARq, PRR, PXR, SAR, SXR | nuclear receptor subfamily 1, group I, member 2 |
C00041495
|
OMIM | preferred title | UniProt |
---|---|---|
#219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
#612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
#208900 | Ataxia-telangiectasia; at |
Q13315
|
#114500 | Colorectal cancer; crc |
P84022
|
#127750 | Dementia, lewy body; dlb |
P37840
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#174800 | Mccune-albright syndrome; mas |
P63092
|
#257200 | Niemann-pick disease, type a |
P17405
|
#607616 | Niemann-pick disease, type b |
P17405
|
#166350 | Osseous heteroplasia, progressive; poh |
P63092
|
#259730 | Osteopetrosis, autosomal recessive 3; optb3 |
P00918
|
#168601 | Parkinson disease 1, autosomal dominant; park1 |
P37840
|
#605543 | Parkinson disease 4, autosomal dominant; park4 |
P37840
|
#168600 | Parkinson disease, late-onset; pd |
P37840
|
#102200 | Pituitary adenoma, growth hormone-secreting |
P63092
|
#103580 | Pseudohypoparathyroidism, type ia; php1a |
P63092
|
#603233 | Pseudohypoparathyroidism, type ib; php1b |
P63092
|
#612462 | Pseudohypoparathyroidism, type ic; php1c |
P63092
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | name | UniProt |
---|---|---|
H00241 | Combined proximal and distal renal tubular acidosis (RTA type 3) |
P00918
(related)
|
H00436 | Osteopetrosis |
P00918
(related)
|
H00599 | 46,XX disorders of sex development (Disorders related to androgen excess) |
P04150
(related)
|
H00137 | Niemann-Pick disease (NPD) typeA and B |
P17405
(related)
|
H00424 | Defects in the degradation of sphingomyelin |
P17405
(related)
|
H00057 | Parkinson's disease (PD) |
P37840
(related)
|
H00066 | Lewy body dementia (LBD) |
P37840
(related)
|
H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
Q13148
(related)
|
H00005 | Chronic lymphocytic leukemia (CLL) |
Q13315
(related)
|
H00064 | Ataxia telangiectasia (AT) |
Q13315
(related)
|
H00094 | DNA repair defects |
Q13315
(related)
|
H00848 | Ataxia with ocular apraxia (AOA) |
Q13315
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
Q9NUW8 (related) |
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|