class name | count |
---|---|
rosids | 2 |
Spermatophyta | 1 |
class name | count |
---|---|
Meliaceae | 2 |
Pinaceae | 1 |
br08003 Category | # of metabolite |
---|---|
Androstane | 1 |
br08003 Category | KEGG ID | KNApSAcK ID |
---|---|---|
Androstane | C00280 | C00003644 |
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 |
---|---|---|---|---|---|---|
C00003644
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Androstenedione
|
CHEMBL274826
CHEMBL1596627 CHEMBL2140059 CHEMBL2311155 |
D000735
|
35 / 46 / 31 | 19 / 2 |
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C00046996
![]() |
6alpha-Hydroxyandrosta-1,4-diene-3,17-dione
|
![]() |
||||
C00047005
![]() |
Androsta-1,4-diene-3,17-dione
/ (+)-Androsta-1,4-diene-3,17-dione |
CHEMBL1078534
CHEMBL1554587 |
C006573
|
5 / 2 / 3 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00003644 C00047005 | 0 / 0 |
P11511 | Cytochrome P450 19A1 | Cytochrome P450 19A1 | C00003644 C00047005 | 2 / 2 |
Q16637 | Survival motor neuron protein | Unclassified protein | C00003644 | 4 / 1 |
Q12809 | Potassium voltage-gated channel subfamily H member 2 | KCNH, Kv10-12.x (Ether-a-go-go) | C00003644 | 2 / 2 |
Q03181 | Peroxisome proliferator-activated receptor delta | NR1C2 | C00003644 | 0 / 0 |
O15245 | Solute carrier family 22 member 1 | Drug uniporter | C00003644 | 0 / 0 |
P02545 | Prelamin-A/C | Unclassified protein | C00003644 | 11 / 10 |
P16473 | Thyrotropin receptor | Glycohormone receptor | C00003644 | 3 / 2 |
P19793 | Retinoic acid receptor RXR-alpha | NR2B1 | C00003644 | 0 / 0 |
P31213 | 3-oxo-5-alpha-steroid 4-dehydrogenase 2 | Oxidoreductase | C00003644 | 1 / 1 |
P54132 | Bloom syndrome protein | Enzyme | C00003644 | 1 / 2 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00003644 | 1 / 0 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00003644 | 0 / 0 |
P04278 | Sex hormone-binding globulin | Secreted protein | C00003644 | 0 / 0 |
P42330 | Aldo-keto reductase family 1 member C3 | Enzyme | C00003644 | 0 / 0 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00003644 | 2 / 0 |
O75496 | Geminin | Unclassified protein | C00003644 | 0 / 0 |
P18405 | 3-oxo-5-alpha-steroid 4-dehydrogenase 1 | Oxidoreductase | C00003644 | 0 / 0 |
P10145 | Interleukin-8 | Secreted protein | C00003644 | 0 / 0 |
P49798 | Regulator of G-protein signaling 4 | Unclassified protein | C00003644 | 2 / 0 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00047005 | 0 / 0 |
P04150 | Glucocorticoid receptor | NR3C1 | C00003644 | 0 / 1 |
Q99700 | Ataxin-2 | Unclassified protein | C00003644 | 1 / 1 |
P37058 | Testosterone 17-beta-dehydrogenase 3 | Enzyme | C00003644 | 1 / 1 |
P28482 | Mitogen-activated protein kinase 1 | Erk | C00003644 | 0 / 0 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00003644 | 3 / 3 |
Q01453 | Peripheral myelin protein 22 | Unclassified protein | C00003644 | 5 / 2 |
P51449 | Nuclear receptor ROR-gamma | Nuclear hormone receptor subfamily 1 group F member 3 | C00003644 | 0 / 0 |
P03372 | Estrogen receptor | NR3A1 | C00003644 | 1 / 1 |
P08185 | Corticosteroid-binding globulin | Secreted protein | C00003644 | 1 / 1 |
P19838 | Nuclear factor NF-kappa-B p105 subunit | Transcription Factor | C00003644 | 0 / 0 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00047005 | 0 / 1 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00003644 | 0 / 0 |
Q6W5P4 | Neuropeptide S receptor | Neuropeptide receptor | C00003644 | 1 / 0 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00003644 | 0 / 0 |
P10275 | Androgen receptor | NR3C4 | C00003644 | 3 / 4 |
P56937 | 3-keto-steroid reductase | Enzyme | C00047005 | 0 / 0 |
Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00003644 | 1 / 1 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
64240 | ABCG5, STSL | ATP-binding cassette, sub-family G (WHITE), member 5 |
C00003644
|
64241 | ABCG8, GBD4, STSL | ATP-binding cassette, sub-family G (WHITE), member 8 |
C00003644
|
8644 | AKR1C3, DD3, DDX, HA1753, HAKRB, HAKRe, HSD17B5, PGFS, hluPGFS | aldo-keto reductase family 1, member C3 (EC:1.3.1.20 1.1.1.188 1.1.1.239 1.1.1.64 1.1.1.112 1.1.1.357) |
C00003644
|
367 | AR, AIS, DHTR, HUMARA, HYSP1, KD, NR3C4, SBMA, SMAX1, TFM | androgen receptor |
C00003644
|
1387 | CREBBP, CBP, KAT3A, RSTS | CREB binding protein (EC:2.3.1.48) |
C00003644
|
1586 | CYP17A1, CPT7, CYP17, P450C17, S17AH | cytochrome P450, family 17, subfamily A, polypeptide 1 (EC:1.14.99.9 4.1.2.30) |
C00003644
|
1588 | CYP19A1, ARO, ARO1, CPV1, CYAR, CYP19, CYPXIX, P-450AROM | cytochrome P450, family 19, subfamily A, polypeptide 1 (EC:1.14.14.1) |
C00003644
|
2938 | GSTA1, GST2, GSTA1-1, GTH1 | glutathione S-transferase alpha 1 (EC:2.5.1.18) |
C00003644
|
2939 | GSTA2, GST2, GSTA2-2, GTA2, GTH2 | glutathione S-transferase alpha 2 (EC:2.5.1.18) |
C00003644
|
2940 | GSTA3, GSTA3-3, GTA3 | glutathione S-transferase alpha 3 (EC:2.5.1.18) |
C00003644
|
3294 | HSD17B2, EDH17B2, HSD17, SDR9C2 | hydroxysteroid (17-beta) dehydrogenase 2 (EC:1.1.1.62 1.1.1.239) |
C00003644
|
3293 | HSD17B3, EDH17B3, SDR12C2 | hydroxysteroid (17-beta) dehydrogenase 3 (EC:1.1.1.64) |
C00003644
|
3283 | HSD3B1, 3BETAHSD, HSD3B, HSDB3, HSDB3A, I, SDR11E1 | hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 1 (EC:1.1.1.145 5.3.3.1) |
C00003644
|
354 | KLK3, APS, KLK2A1, PSA, hK3 | kallikrein-related peptidase 3 (EC:3.4.21.77) |
C00003644
|
3972 | LHB, CGB4, LSH-B, hLHB | luteinizing hormone beta polypeptide |
C00003644
|
2475 | MTOR, FRAP, FRAP1, FRAP2, RAFT1, RAPT1 | mechanistic target of rapamycin (serine/threonine kinase) (EC:2.7.11.1) |
C00003644
|
10499 | NCOA2, GRIP1, KAT13C, NCoA-2, SRC2, TIF2, bHLHe75 | nuclear receptor coactivator 2 |
C00003644
|
8202 | NCOA3, ACTR, AIB-1, AIB1, CAGH16, CTG26, KAT13B, RAC3, SRC-3, SRC3, TNRC14, TNRC16, TRAM-1, bHLHe42, pCIP | nuclear receptor coactivator 3 (EC:2.3.1.48) |
C00003644
|
7124 | TNF, DIF, TNF-alpha, TNFA, TNFSF2 | tumor necrosis factor |
C00003644
|
OMIM | preferred title | UniProt |
---|---|---|
#264300 | 17-beta hydroxysteroid dehydrogenase iii deficiency |
P37058
|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
#300068 | Androgen insensitivity syndrome; ais |
P10275
|
#312300 | Androgen insensitivity, partial; pais |
P10275
|
#613546 | Aromatase deficiency |
P11511
|
#139300 | Aromatase excess syndrome; aexs |
P11511
|
#608584 | Asthma-related traits, susceptibility to, 2 |
Q6W5P4
|
#210900 | Bloom syndrome; blm |
P54132
|
#115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
#212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
#118300 | Charcot-marie-tooth disease and deafness |
Q01453
|
#605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
#118220 | Charcot-marie-tooth disease, demyelinating, type 1a; cmt1a |
Q01453
|
#114500 | Colorectal cancer; crc |
P84022
|
#611489 | Corticosteroid-binding globulin deficiency |
P08185
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#615363 | Estrogen resistance; estrr |
P03372
|
#139393 | Guillain-barre syndrome, familial; gbs |
Q01453
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#603373 | Hyperthyroidism, familial gestational |
P16473
|
#609152 | Hyperthyroidism, nonautoimmune |
P16473
|
#145900 | Hypertrophic neuropathy of dejerine-sottas |
Q01453
|
#275200 | Hypothyroidism, congenital, nongoitrous, 1; chng1 |
P16473
|
#151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#613688 | Long qt syndrome 2; lqt2 |
Q12809
|
#248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
#300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
#300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
#613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
#159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#162500 | Neuropathy, hereditary, with liability to pressure palsies; hnpp |
Q01453
|
#264600 | Pseudovaginal perineoscrotal hypospadias; ppsh |
P31213
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#604906 | Schizophrenia 9; sczd9 |
P49798
|
#181500 | Schizophrenia; sczd |
P49798
|
#609620 | Short qt syndrome 1; sqt1 |
Q12809
|
#313200 | Spinal and bulbar muscular atrophy, x-linked 1; smax1 |
P10275
|
#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
|
KEGG | name | UniProt |
---|---|---|
H00264 | Charcot-Marie-Tooth disease (CMT) |
P02545
(related)
Q01453 (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)
|
H00026 | Endometrial Cancer |
P03372
(marker)
|
H00599 | 46,XX disorders of sex development (Disorders related to androgen excess) |
P04150
(related)
P11511 (related) |
H01163 | Corticosteroid-binding globulin (CBG) deficiency |
P08185
(related)
|
H00036 | Osteosarcoma |
P08684
(marker)
|
H00024 | Prostate cancer |
P10275
(related)
|
H00062 | Spinal and bulbar muscular atrophy (SBMA) |
P10275
(related)
|
H00608 | 46,XY disorders of sex development (Disorders in androgen synthesis or action) |
P10275
(related)
P31213 (related) P37058 (related) |
H00609 | 46,XY disorders of sex development (Other) |
P10275
(related)
|
H00794 | Aromatase excess syndrome |
P11511
(related)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P16473
(related)
|
H01269 | Congenital hyperthyroidism |
P16473
(related)
|
H00094 | DNA repair defects |
P54132
(related)
|
H00296 | Defects in RecQ helicases |
P54132
(related)
|
H01296 | Hereditary neuropathy with liability to pressure palsies (HNPP) |
Q01453
(related)
|
H00720 | Long QT syndrome |
Q12809
(related)
|
H00725 | Short QT syndrome |
Q12809
(related)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
Q13148
(related)
|
H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|
H00480 | Non-syndromic X-linked mental retardation |
Q99714
(related)
|
H00658 | Syndromic X-linked mental retardation |
Q99714
(related)
|
H00925 | 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency |
Q99714
(related)
|