Species

KNApSAcK Entry

Organism name Lentinus edodes Sing.
Genus Lentinus
Family Polyporaceae
Kingdom Fungi

NCBI taxonomy

Entry

Linked NCBI taxonomy name Lentinus
Linked NCBI taxonomy ID 5357
Linked level genus

Family

Family in NCBI taxonomy Lentinaceae
ID 83234

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Fungi
ID 4751

Plant class

Plant class
ID

Metabolite list (2)

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 External link 512 Octanol
/ n-Octanol
/ 1-Octanol
/ Octan-1-ol
CHEMBL26215
D020003
5 / 6 / 5 2 / 0 No. 1749
C00029423 External link 512 1-Octen-3-ol
C038844
0 / 1 No. 3536

Human Protein / Gene in interactions

5 ChEMBL Protein in interactions

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

2 Gene in CTD interactions

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

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (6)

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 DISEASE (5)

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)

Diseases related to CTD interactions

1 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D020258 Neurotoxicity Syndromes C00029423