Species

KNApSAcK Entry

Organism name Diosma crenulata
Genus Diosma
Family Rutaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Diosma
Linked NCBI taxonomy ID 378921
Linked level genus

Family

Family in NCBI taxonomy Rutaceae
ID 23513

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (1)

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
C00004362 External link 512 Diosmin
/ Luteolin 4'-methyl ether 7-rutinoside
/ 5,7,3'-Trihydroxy-4'-methoxyflavone 7-O-rutinoside
CHEMBL231884
CHEMBL1512770
CHEMBL1707291
D004145
20 / 8 / 14 1 / 5 No. 1 No. 15

Human Protein / Gene in interactions

20 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P06746 DNA polymerase beta Enzyme C00004362 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00004362 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00004362 2 / 3
P00352 Retinal dehydrogenase 1 Enzyme C00004362 0 / 0
P39748 Flap endonuclease 1 Enzyme C00004362 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00004362 0 / 0
O75496 Geminin Unclassified protein C00004362 0 / 0
P40763 Signal transducer and activator of transcription 3 Transcription Factor C00004362 1 / 2
Q9Y253 DNA polymerase eta Enzyme C00004362 1 / 1
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00004362 1 / 2
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00004362 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00004362 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00004362 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00004362 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00004362 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00004362 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00004362 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00004362 1 / 1
O00255 Menin Unclassified protein C00004362 2 / 5
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00004362 0 / 0

1 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
196 AHR, bHLHe76 aryl hydrocarbon receptor C00004362

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (8)

OMIM preferred title UniProt
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#147060 Hyper-ige recurrent infection syndrome, autosomal dominant P40763
#145000 Hyperparathyroidism 1; hrpt1 O00255
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (14)

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)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H00016 Oral cancer P40763 (related)
H00107 Other well-defined immunodeficiency syndromes P40763 (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) Q9NUW8 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

5 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D003921 Diabetes Mellitus, Experimental C00004362
D003924 Diabetes Mellitus, Type 2 C00004362
D056486 Drug-Induced Liver Injury C00004362
D006501 Hepatic Encephalopathy C00004362
D007565 Jaundice C00004362