Organism name | Lonchocarpus miniflorus |
---|---|
Genus | Lonchocarpus |
Family | Fabaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Lonchocarpus |
---|---|
Linked NCBI taxonomy ID | 3925 |
Linked level | genus |
Family in NCBI taxonomy | Fabaceae |
---|---|
ID | 3803 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | rosids |
---|---|
ID | 71275 |
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 |
---|---|---|---|---|---|---|---|---|
C00000954
![]() |
Senegalensein
/ Lonchocarpol A / 6,8-Diprenylnaringenin |
CHEMBL477969
CHEMBL1545584 |
C068505
|
16 / 26 / 18 | No. 19 | No. 14 |
![]() |
|
C00008263
![]() |
5,4'-Dihydroxy-7-methoxy-6-C-prenylflavanone
|
No. 28 | No. 14 |
![]() |
||||
C00008261
![]() |
Minimiflorin
|
CHEMBL464778
|
No. 39 |
![]() |
||||
C00008262
![]() |
Lupinifolin
|
CHEMBL559980
|
No. 39 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P17861 | X-box-binding protein 1 | Unclassified protein | C00000954 | 1 / 0 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00000954 | 0 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00000954 | 1 / 1 |
P06746 | DNA polymerase beta | Enzyme | C00000954 | 0 / 0 |
P04062 | Glucosylceramidase | Enzyme | C00000954 | 6 / 4 |
P39748 | Flap endonuclease 1 | Enzyme | C00000954 | 0 / 0 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00000954 | 2 / 0 |
O75496 | Geminin | Unclassified protein | C00000954 | 0 / 0 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00000954 | 0 / 0 |
P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00000954 | 7 / 3 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00000954 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00000954 | 4 / 3 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00000954 | 1 / 0 |
O00255 | Menin | Unclassified protein | C00000954 | 2 / 5 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00000954 | 1 / 2 |
Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00000954 | 1 / 1 |
OMIM | preferred title | UniProt |
---|---|---|
#219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
#612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
#114500 | Colorectal cancer; crc |
P84022
|
#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
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#612371 | Major affective disorder 7; mafd7 |
P17861
|
#174800 | Mccune-albright syndrome; mas |
P63092
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
#166350 | Osseous heteroplasia, progressive; poh |
P63092
|
#168600 | Parkinson disease, late-onset; pd |
P04062
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#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
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
KEGG | name | UniProt |
---|---|---|
H00033 | Adrenal carcinoma |
O00255
(related)
|
H00034 | Carcinoid |
O00255
(related)
|
H00045 | Malignant islet cell carcinoma |
O00255
(related)
|
H00246 | Primary hyperparathyroidism |
O00255
(related)
|
H01102 | Pituitary adenomas |
O00255
(related)
|
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)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
Q13148 (related) |
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
H00501 | Fibrous dysplasia, polyostotic |
P63092
(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)
|