Species

KNApSAcK Entry

Organism name Cladonia rangiferina
Genus Cladonia
Family Cladoniaceae
Kingdom Fungi

NCBI taxonomy

Entry

Linked NCBI taxonomy name Cladonia rangiferina
Linked NCBI taxonomy ID 111670
Linked level species

Family

Family in NCBI taxonomy Cladoniaceae
ID 5198

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Fungi
ID 4751

Plant class

Plant class
ID

Metabolite list (11)

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
C00023300 External link 512 Imbricatoloic acid
CHEMBL2048004
No. 143
C00023303 External link 512 Junicedric acid
CHEMBL2048915
No. 143
C00030453 External link 512 Hanagokenol A
No. 355
C00030792 External link 512 Montbretol
/ 6,12-Dihydroxyabieta-5,8,11,13-tetraen-7-one
CHEMBL469670
No. 1418
C00029760 External link 512 Atranol
CHEMBL223288
No. 2076
C00029788 External link 512 Barbatic acid
CHEMBL1902081
6 / 15 / 8 No. 3861
C00030489 External link 512 Homosekikaic acid
No. 4311
C00030010 External link 512 Condidymic acid
No. 4311
C00030127 External link 512 Didymic acid
No. 4311
C00030454 External link 512 Hanagokenol B
No. 4752
C00030875 External link 512 Obtuanhydride
/ (-)-Obtuanhydride
No. 4752

Human Protein / Gene in interactions

6 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P37840 Alpha-synuclein Unclassified protein C00029788 4 / 2
P11473 Vitamin D3 receptor NR1I1 C00029788 2 / 3
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00029788 2 / 0
O75496 Geminin Unclassified protein C00029788 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00029788 7 / 3
Q9UNA4 DNA polymerase iota Enzyme C00029788 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (15)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#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
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#166350 Osseous heteroplasia, progressive; poh P63092
#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
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (8)

KEGG name UniProt
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (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)