Organism name | Lentinus edodes Sing. |
---|---|
Genus | Lentinus |
Family | Polyporaceae |
Kingdom | Fungi |
Linked NCBI taxonomy name | Lentinus |
---|---|
Linked NCBI taxonomy ID | 5357 |
Linked level | genus |
Family in NCBI taxonomy | Lentinaceae |
---|---|
ID | 83234 |
Kingdom (Superkingdom) in NCBI taxonomy | Fungi |
---|---|
ID | 4751 |
Plant class | |
---|---|
ID |
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 |
---|---|---|---|---|---|---|---|---|
C00001264
![]() |
Octanol
/ n-Octanol / 1-Octanol / Octan-1-ol |
CHEMBL26215
|
D020003
|
5 / 6 / 5 | 2 / 0 | No. 1749 |
![]() |
|
C00029423
![]() |
1-Octen-3-ol
|
C038844
|
0 / 1 | No. 3536 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P10828 | Thyroid hormone receptor beta | NR1A2 | C00001264 | 3 / 1 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00001264 | 0 / 0 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00001264 | 0 / 0 |
P04150 | Glucocorticoid receptor | NR3C1 | C00001264 | 0 / 1 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00001264 | 3 / 3 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
128 | ADH5, ADH-3, ADHX, FALDH, FDH, GSH-FDH, GSNOR | alcohol dehydrogenase 5 (class III), chi polypeptide (EC:1.1.1.1 1.1.1.284) |
C00001264
|
1080 | CFTR, ABC35, ABCC7, CF, CFTR/MRP, MRP7, TNR-CFTR, dJ760C5.1 | cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7) (EC:3.6.3.49) |
C00001264
|
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
#300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
#188570 | Thyroid hormone resistance, generalized, autosomal dominant; grth |
P10828
|
#274300 | Thyroid hormone resistance, generalized, autosomal recessive; grth |
P10828
|
#145650 | Thyroid hormone resistance, selective pituitary; prth |
P10828
|
KEGG | name | UniProt |
---|---|---|
H00599 | 46,XX disorders of sex development (Disorders related to androgen excess) |
P04150
(related)
|
H00249 | Thyroid hormone resistance syndrome |
P10828
(related)
|
H00480 | Non-syndromic X-linked mental retardation |
Q99714
(related)
|
H00658 | Syndromic X-linked mental retardation |
Q99714
(related)
|
H00925 | 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency |
Q99714
(related)
|