class name | count |
---|
class name | count |
---|---|
Corticiaceae | 2 |
Meruliaceae | 1 |
Auriscalpiaceae | 1 |
Russulaceae | 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 |
---|---|---|---|---|---|---|
C00003155
![]() |
Isovelleral
|
CHEMBL518292
CHEMBL1995288 |
C089286
|
29 / 34 / 27 |
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|
C00018191
![]() |
Merulidial
/ (-)-Merulidial |
C017491
|
![]() |
|||
C00021522
![]() |
Merulactone
|
![]() |
||||
C00021523
![]() |
Merulanic acid
|
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q16637 | Survival motor neuron protein | Unclassified protein | C00003155 | 4 / 1 |
P17861 | X-box-binding protein 1 | Unclassified protein | C00003155 | 1 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00003155 | 1 / 1 |
P06746 | DNA polymerase beta | Enzyme | C00003155 | 0 / 0 |
Q13315 | Serine-protein kinase ATM | Atypical serine/threonine protein kinase PIKK subfamily | C00003155 | 1 / 4 |
P02545 | Prelamin-A/C | Unclassified protein | C00003155 | 11 / 10 |
P37840 | Alpha-synuclein | Unclassified protein | C00003155 | 4 / 2 |
P54132 | Bloom syndrome protein | Enzyme | C00003155 | 1 / 2 |
O95977 | Sphingosine 1-phosphate receptor 4 | EDG receptor | C00003155 | 0 / 0 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00003155 | 0 / 0 |
P21453 | Sphingosine 1-phosphate receptor 1 | EDG receptor | C00003155 | 0 / 0 |
P42858 | Huntingtin | Unclassified protein | C00003155 | 1 / 1 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00003155 | 2 / 0 |
O75496 | Geminin | Unclassified protein | C00003155 | 0 / 0 |
P51151 | Ras-related protein Rab-9A | Unclassified protein | C00003155 | 0 / 0 |
Q9Y2T6 | G-protein coupled receptor 55 | Lysophosphatidylinositol receptor | C00003155 | 0 / 0 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00003155 | 0 / 0 |
P28482 | Mitogen-activated protein kinase 1 | Erk | C00003155 | 0 / 0 |
O75762 | Transient receptor potential cation channel subfamily A member 1 | Unclassified protein | C00003155 | 1 / 0 |
O15118 | Niemann-Pick C1 protein | Unclassified protein | C00003155 | 1 / 1 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00003155 | 0 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00003155 | 0 / 0 |
Q6W5P4 | Neuropeptide S receptor | Neuropeptide receptor | C00003155 | 1 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00003155 | 4 / 3 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00003155 | 0 / 0 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00003155 | 0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00003155 | 0 / 0 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00003155 | 1 / 0 |
P01215 | Glycoprotein hormones alpha chain | Unclassified protein | C00003155 | 0 / 3 |
OMIM | preferred title | UniProt |
---|---|---|
#608584 | Asthma-related traits, susceptibility to, 2 |
Q6W5P4
|
#208900 | Ataxia-telangiectasia; at |
Q13315
|
#210900 | Bloom syndrome; blm |
P54132
|
#115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
#212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
#605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
#114500 | Colorectal cancer; crc |
P84022
|
#127750 | Dementia, lewy body; dlb |
P37840
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#615040 | Episodic pain syndrome, familial, 1; feps1 |
O75762
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#143100 | Huntington disease; hd |
P42858
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#612371 | Major affective disorder 7; mafd7 |
P17861
|
#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
|
#257220 | Niemann-pick disease, type c1; npc1 |
O15118
|
#168601 | Parkinson disease 1, autosomal dominant; park1 |
P37840
|
#605543 | Parkinson disease 4, autosomal dominant; park4 |
P37840
|
#168600 | Parkinson disease, late-onset; pd |
P37840
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#253300 | Spinal muscular atrophy, type i; sma1 |
Q16637
|
#253550 | Spinal muscular atrophy, type ii; sma2 |
Q16637
|
#253400 | Spinal muscular atrophy, type iii; sma3 |
Q16637
|
#271150 | Spinal muscular atrophy, type iv; sma4 |
Q16637
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
KEGG | name | UniProt |
---|---|---|
H00136 | Niemann-Pick disease type C (NPC) |
O15118
(related)
|
H00081 | Hashimoto's thyroiditis |
P01215
(marker)
|
H00082 | Graves' disease |
P01215
(marker)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P01215
(marker)
|
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)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00057 | Parkinson's disease (PD) |
P37840
(related)
|
H00066 | Lewy body dementia (LBD) |
P37840
(related)
|
H00059 | Huntington's disease (HD) |
P42858
(related)
|
H00094 | DNA repair defects |
P54132
(related)
Q13315 (related) |
H00296 | Defects in RecQ helicases |
P54132
(related)
|
H00005 | Chronic lymphocytic leukemia (CLL) |
Q13315
(related)
|
H00064 | Ataxia telangiectasia (AT) |
Q13315
(related)
|
H00848 | Ataxia with ocular apraxia (AOA) |
Q13315
(related)
|
H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|