PCIDB

Gabarnaudia tholispora

Species

KNApSAcK Entry

Organism name Gabarnaudia tholispora
Genus
Family
Kingdom

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
C00023903 External link 512 Fusidic acid
CHEMBL117110
CHEMBL383466
CHEMBL374975
CHEMBL1334456
CHEMBL1477084
CHEMBL1552107
CHEMBL1619349
CHEMBL1620692
CHEMBL1625992
CHEMBL2068923
D005672
10 / 11 / 11 1 / 14 No. 725

Human Protein / Gene in interactions

10 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P02768 Serum albumin Secreted protein C00023903 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00023903 2 / 3
P39748 Flap endonuclease 1 Enzyme C00023903 0 / 0
O75496 Geminin Unclassified protein C00023903 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00023903 7 / 3
P83916 Chromobox protein homolog 1 Unclassified protein C00023903 0 / 0
Q92887 Canalicular multispecific organic anion transporter 1 Unclassified protein C00023903 1 / 1
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00023903 0 / 0
Q13951 Core-binding factor subunit beta Unclassified protein C00023903 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00023903 1 / 4

1 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
8647 ABCB11, ABC16, BRIC2, BSEP, PFIC-2, PFIC2, PGY4, SPGP ATP-binding cassette, sub-family B (MDR/TAP), member 11 C00023903

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (11)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#237500 Dubin-johnson syndrome; djs Q92887
#174800 Mccune-albright syndrome; mas P63092
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#166350 Osseous heteroplasia, progressive; poh P63092
#102200 Pituitary adenoma, growth hormone-secreting P63092
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#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 (11)

KEGG name UniProt
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00004 Chronic myeloid leukemia (CML) Q01196 (related)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00208 Hyperbilirubinemia Q92887 (related)

Diseases related to CTD interactions

14 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D058186 Acute Kidney Injury C00023903
D000756 Anemia, Sideroblastic C00023903
D002779 Cholestasis C00023903
D003424 Crohn Disease C00023903
D004697 Endocarditis, Bacterial C00023903
D006932 Hyperbilirubinemia C00023903
D006996 Hypocalcemia C00023903
D007565 Jaundice C00023903
D009325 Nausea C00023903
D010019 Osteomyelitis C00023903
D012206 Rhabdomyolysis C00023903
D013203 Staphylococcal Infections C00023903
D013924 Thrombophlebitis C00023903
D014552 Urinary Tract Infections C00023903