| class name | count |
|---|---|
| asterids | 6 |
| rosids | 6 |
| Spermatophyta | 3 |
| eudicotyledons | 2 |
| Euphyllophyta | 1 |
| class name | count |
|---|---|
| Aspergillaceae | 6 |
| Meliaceae | 3 |
| Ericaceae | 2 |
| Brassicaceae | 2 |
| Solanaceae | 2 |
| Pteridaceae | 1 |
| Saxifragaceae | 1 |
| Podocarpaceae | 1 |
| Apiaceae | 1 |
| Didymellaceae | 1 |
| Pinaceae | 1 |
| Amaranthaceae | 1 |
| Asteraceae | 1 |
| Moraceae | 1 |
| Hypocreaceae | 1 |
| Cupressaceae | 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 |
|---|---|---|---|---|---|---|
|
C00002645
|
p-Cresol
/ 4-Methylphenol |
CHEMBL16645
|
C032538
|
8 / 4 / 4 | 10 / 4 |
|
|
C00002649
|
Gentisyl alcohol
|
CHEMBL448800
|
C004771
|
|
||
|
C00002660
|
4-Methylcatechol
|
CHEMBL158766
|
C018599
|
1 / 2 |
|
|
|
C00002661
|
Orcinol
|
CHEMBL110059
|
C005282
|
1 / 4 / 2 |
|
|
|
C00023720
|
Toluquinol
|
CHEMBL450917
|
C062397
|
|
||
|
C00030878
|
o-Cresol
|
CHEMBL46931
|
C034047
|
4 / 9 / 3 | 1 / 4 |
|
|
C00035128
|
m-Cresol
/ m-Oxytoluene |
CHEMBL298312
|
C042041
|
6 / 4 / 1 | 1 / 3 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00002645 C00030878 C00035128 | 0 / 0 |
| P22303 | Acetylcholinesterase | Hydrolase | C00002645 C00035128 | 1 / 0 |
| P14679 | Tyrosinase | Oxidoreductase | C00002661 | 4 / 2 |
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00030878 | 2 / 0 |
| P50225 | Sulfotransferase 1A1 | Enzyme | C00002645 | 0 / 0 |
| O60656 | UDP-glucuronosyltransferase 1-9 | Enzyme | C00002645 | 0 / 0 |
| P10145 | Interleukin-8 | Secreted protein | C00002645 | 0 / 0 |
| P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00030878 | 7 / 3 |
| Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00035128 | 0 / 0 |
| Q96RI1 | Bile acid receptor | NR1H4 | C00030878 | 0 / 0 |
| P51449 | Nuclear receptor ROR-gamma | Nuclear hormone receptor subfamily 1 group F member 3 | C00002645 | 0 / 0 |
| P10828 | Thyroid hormone receptor beta | NR1A2 | C00035128 | 3 / 1 |
| P19224 | UDP-glucuronosyltransferase 1-6 | Enzyme | C00002645 | 0 / 0 |
| P19793 | Retinoic acid receptor RXR-alpha | NR2B1 | C00035128 | 0 / 0 |
| P10275 | Androgen receptor | NR3C4 | C00002645 | 3 / 4 |
| Q9UBT6 | DNA polymerase kappa | Enzyme | C00035128 | 0 / 0 |
| gene | gene name | gene description | KNApSAcK metabolite in interactions |
|---|---|---|---|
| 213 | ALB, PRO0883, PRO0903, PRO1341 | albumin |
C00002645
C00030878
|
| 50848 | F11R, CD321, JAM, JAM1, JAMA, JCAM, KAT, PAM-1 | F11 receptor |
C00002645
|
| 6376 | CX3CL1, ABCD-3, C3Xkine, CXC3, CXC3C, NTN, NTT, SCYD1, fractalkine, neurotactin | chemokine (C-X3-C motif) ligand 1 |
C00002645
|
| 1544 | CYP1A2, CP12, P3-450, P450(PA) | cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) |
C00002645
|
| 1565 | CYP2D6, CPD6, CYP2D, CYP2D7AP, CYP2D7BP, CYP2D7P2, CYP2D8P2, CYP2DL1, CYPIID6, P450-DB1, P450C2D, P450DB1 | cytochrome P450, family 2, subfamily D, polypeptide 6 (EC:1.14.14.1) |
C00002645
|
| 1571 | CYP2E1, CPE1, CYP2E, P450-J, P450C2E | cytochrome P450, family 2, subfamily E, polypeptide 1 (EC:1.14.13.n7) |
C00002645
|
| 1312 | COMT | catechol-O-methyltransferase (EC:2.1.1.6) |
C00002660
|
| 3383 | ICAM1, BB2, CD54, P3.58 | intercellular adhesion molecule 1 |
C00002645
|
| 3553 | IL1B, IL-1, IL1-BETA, IL1F2 | interleukin 1, beta |
C00002645
|
| 7124 | TNF, DIF, TNF-alpha, TNFA, TNFSF2 | tumor necrosis factor |
C00002645
|
| 7412 | VCAM1, CD106, INCAM-100 | vascular cell adhesion molecule 1 |
C00002645
|
| 6329 | SCN4A, HOKPP2, HYKPP, HYPP, NAC1A, Na(V)1.4, Nav1.4, SkM1 | sodium channel, voltage-gated, type IV, alpha subunit |
C00035128
|
| OMIM | preferred title | UniProt |
|---|---|---|
| #219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
| #103470 | Albinism, ocular, with sensorineural deafness |
P14679
|
| #203100 | Albinism, oculocutaneous, type ia; oca1a |
P14679
|
| #606952 | Albinism, oculocutaneous, type ib; oca1b |
P14679
|
| #300068 | Androgen insensitivity syndrome; ais |
P10275
|
| #312300 | Androgen insensitivity, partial; pais |
P10275
|
| #114500 | Colorectal cancer; crc |
P84022
|
| #613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
| #174800 | Mccune-albright syndrome; mas |
P63092
|
| #166350 | Osseous heteroplasia, progressive; poh |
P63092
|
| #102200 | Pituitary adenoma, growth hormone-secreting |
P63092
|
| #103580 | Pseudohypoparathyroidism, type ia; php1a |
P63092
|
| #603233 | Pseudohypoparathyroidism, type ib; php1b |
P63092
|
| #612462 | Pseudohypoparathyroidism, type ic; php1c |
P63092
|
| #601800 | Skin/hair/eye pigmentation, variation in, 3; shep3 |
P14679
|
| #313200 | Spinal and bulbar muscular atrophy, x-linked 1; smax1 |
P10275
|
| #188570 | Thyroid hormone resistance, generalized, autosomal dominant; grth |
P10828
|
| #274300 | Thyroid hormone resistance, generalized, autosomal recessive; grth |
P10828
|
| #145650 | Thyroid hormone resistance, selective pituitary; prth |
P10828
|
| #112100 | Yt blood group antigen |
P22303
|
| KEGG | name | UniProt |
|---|---|---|
| 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)
|
| H00609 | 46,XY disorders of sex development (Other) |
P10275
(related)
|
| H00249 | Thyroid hormone resistance syndrome |
P10828
(related)
|
| H00168 | Oculocutaneous albinism (OCA) |
P14679
(related)
|
| H00038 | Malignant melanoma |
P14679
(marker)
|
| H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
| H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
| H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|
| MESH or OMIM | name |
KNApSAcK
metabolite |
|---|---|---|
| D003929 | Diabetic Neuropathies |
C00002660
|
| D010523 | Peripheral Nervous System Diseases |
C00002660
|
| D002318 | Cardiovascular Diseases |
C00002645
|
| D003873 | Dermatitis, Exfoliative |
C00002645
|
| D006965 | Hyperplasia |
C00002645
|
| D007674 | Kidney Diseases |
C00002645
|
| D001836 | Body Weight Changes |
C00030878
|
| D017449 | Dermatitis, Allergic Contact |
C00030878
|
| D014202 | Tremor |
C00030878
|
| D015431 | Weight Loss |
C00030878
|
| D002057 | Burns, Chemical |
C00035128
|
| D056486 | Drug-Induced Liver Injury |
C00035128
|
| D006967 | Hypersensitivity |
C00035128
|