class name | count |
---|---|
Spermatophyta | 13 |
class name | count |
---|---|
Podocarpaceae | 13 |
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 |
---|---|---|---|---|---|---|
C00000268
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Nagilactone A
|
CHEMBL1381439
|
13 / 20 / 13 |
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||
C00000269
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Nagilactone B
|
CHEMBL1586581
|
19 / 26 / 18 |
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||
C00000270
![]() |
Nagilactone C
|
CHEMBL176006
CHEMBL487996 |
C004552
|
![]() |
||
C00000271
![]() |
Nagilactone D
|
![]() |
||||
C00000276
![]() |
Hallactone A
|
C007900
|
![]() |
|||
C00000286
![]() |
Sellowin C
|
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q16637 | Survival motor neuron protein | Unclassified protein | C00000268 C00000269 | 4 / 1 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00000268 C00000269 | 1 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00000268 C00000269 | 1 / 1 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00000268 C00000269 | 0 / 0 |
P02545 | Prelamin-A/C | Unclassified protein | C00000268 C00000269 | 11 / 10 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00000268 C00000269 | 0 / 0 |
P42858 | Huntingtin | Unclassified protein | C00000268 C00000269 | 1 / 1 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00000268 C00000269 | 2 / 0 |
O75496 | Geminin | Unclassified protein | C00000268 C00000269 | 0 / 0 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00000268 C00000269 | 0 / 0 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00000268 | 0 / 0 |
P51151 | Ras-related protein Rab-9A | Unclassified protein | C00000269 | 0 / 0 |
O15118 | Niemann-Pick C1 protein | Unclassified protein | C00000269 | 1 / 1 |
O75030 | Microphthalmia-associated transcription factor | Unclassified protein | C00000269 | 4 / 4 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00000269 | 1 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00000268 | 0 / 0 |
P06746 | DNA polymerase beta | Enzyme | C00000268 | 0 / 0 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00000269 | 0 / 0 |
Q8IUX4 | DNA dC->dU-editing enzyme APOBEC-3F | Enzyme | C00000269 | 0 / 0 |
Q00653 | Nuclear factor NF-kappa-B p100 subunit | Transcription Factor | C00000269 | 0 / 0 |
Q04206 | Transcription factor p65 | Transcription Factor | C00000269 | 0 / 0 |
P19838 | Nuclear factor NF-kappa-B p105 subunit | Transcription Factor | C00000269 | 0 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#103470 | Albinism, ocular, with sensorineural deafness |
O75030
|
#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
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#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
|
#248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
#614456 | Melanoma, cutaneous malignant, susceptibility to, 8; cmm8 |
O75030
|
#613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
#159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#257220 | Niemann-pick disease, type c1; npc1 |
O15118
|
#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
|
#103500 | Tietz syndrome |
O75030
|
#193510 | Waardenburg syndrome, type 2a; ws2a |
O75030
|
KEGG | name | UniProt |
---|---|---|
H00136 | Niemann-Pick disease type C (NPC) |
O15118
(related)
|
H00038 | Malignant melanoma |
O75030
(related)
O75030 (marker) |
H00169 | Ocular albinism |
O75030
(related)
|
H00759 | Waardenburg syndrome (WS) |
O75030
(related)
|
H01187 | Tietz syndrome |
O75030
(related)
|
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)
|
H00059 | Huntington's disease (HD) |
P42858
(related)
|
H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|