KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (12)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
figure
C00007433 External link 512 1,16-Dihydroxyhexadecane
CHEMBL448715
C00007437 External link 512 1,18-Octadecanediol
C00029422 External link 512 1-Octadecanol
/ Octadecan-1-ol
CHEMBL24640
C009316
3 / 11 / 10
C00030165 External link 512 Eicosane
C050821
C00030470 External link 512 Heneicosane
C00030805 External link 512 1-Docosanol
/ n-Docosanol
CHEMBL1200453
C529236
1 / 0 / 0
C00030827 External link 512 Nonadecane
C061580
C00030879 External link 512 Octadecane
C022883
C00032409 External link 512 Tricosane
C00035094 External link 512 1-Eicosanol
/ Eicosan-1-ol
CHEMBL451717
C00035592 External link 512 Docosane
C470023
C00036250 External link 512 1-Docosene

Human Protein / Gene in interactions

4 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P02545 Prelamin-A/C Unclassified protein C00029422 11 / 10
Q92830 Histone acetyltransferase KAT2A Enzyme C00030805 0 / 0
O75496 Geminin Unclassified protein C00029422 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00029422 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (11)

OMIM preferred title UniProt
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#275210 Restrictive dermopathy, lethal P02545

KEGG DISEASE (10)

KEGG name UniProt
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
H00563 Emery-Dreifuss muscular dystrophy P02545 (related)
H00590 Congenital muscular dystrophies (CMD/MDC) P02545 (related)
H00593 Limb-girdle muscular dystrophy (LGMD) P02545 (related)
H00601 Hutchinson-Gilford progeria syndrome P02545 (related)
H00663 Restrictive dermopathy P02545 (related)
H00665 Mandibuloacral dysplasia P02545 (related)
H01216 Left ventricular noncompaction (LVNC) P02545 (related)