class name | count |
---|---|
rosids | 1 |
class name | count |
---|---|
Rutaceae | 1 |
br08003 Category | # of metabolite |
---|---|
Quinoline alkaloids | 1 |
br08003 Category | KEGG ID | KNApSAcK ID |
---|---|---|
Quinoline alkaloids | C10649 | C00002142 |
KNApSAcK ID | name | ChEMBL link | CTD link |
# of proteins in
ChEMBL interaction / related OMIM / related KEGG DISEASE |
# of genes in
CTD interaction / related diseases |
figure |
---|---|---|---|---|---|---|
C00002142
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Bucharaine
|
CHEMBL1338870
|
7 / 10 / 13 |
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accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q16637 | Survival motor neuron protein | Unclassified protein | C00002142 | 4 / 1 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00002142 | 1 / 0 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00002142 | 2 / 2 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00002142 | 0 / 0 |
O00255 | Menin | Unclassified protein | C00002142 | 2 / 5 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00002142 | 1 / 2 |
P01215 | Glycoprotein hormones alpha chain | Unclassified protein | C00002142 | 0 / 3 |
OMIM | preferred title | UniProt |
---|---|---|
#119900 | Digital clubbing, isolated congenital |
P15428
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#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
|
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)
|
H00081 | Hashimoto's thyroiditis |
P01215
(marker)
|
H00082 | Graves' disease |
P01215
(marker)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P01215
(marker)
|
H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(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)
|
H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
|