class name | count |
---|---|
asterids | 14 |
rosids | 8 |
Embryophyta | 4 |
class name | count |
---|---|
Asteraceae | 9 |
Brassicaceae | 4 |
Frullaniaceae | 4 |
Solanaceae | 2 |
Boraginaceae | 2 |
Clusiaceae | 1 |
Lamiaceae | 1 |
Fabaceae | 1 |
Cistaceae | 1 |
Hypericaceae | 1 |
br08003 Category | # of metabolite |
---|
br08003 Category | KEGG ID | KNApSAcK ID |
---|
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
![]() |
1,16-Dihydroxyhexadecane
|
CHEMBL448715
|
![]() |
|||
C00007437
![]() |
1,18-Octadecanediol
|
![]() |
||||
C00029422
![]() |
1-Octadecanol
/ Octadecan-1-ol |
CHEMBL24640
|
C009316
|
3 / 11 / 10 |
![]() |
|
C00030165
![]() |
Eicosane
|
C050821
|
![]() |
|||
C00030470
![]() |
Heneicosane
|
![]() |
||||
C00030805
![]() |
1-Docosanol
/ n-Docosanol |
CHEMBL1200453
|
C529236
|
1 / 0 / 0 |
![]() |
|
C00030827
![]() |
Nonadecane
|
C061580
|
![]() |
|||
C00030879
![]() |
Octadecane
|
C022883
|
![]() |
|||
C00032409
![]() |
Tricosane
|
![]() |
||||
C00035094
![]() |
1-Eicosanol
/ Eicosan-1-ol |
CHEMBL451717
|
![]() |
|||
C00035592
![]() |
Docosane
|
C470023
|
![]() |
|||
C00036250
![]() |
1-Docosene
|
![]() |
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 |
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 | 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)
|