KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (7)

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 External link 512 p-Cresol
/ 4-Methylphenol
CHEMBL16645
C032538
8 / 4 / 4 10 / 4
C00002649 External link 512 Gentisyl alcohol
CHEMBL448800
C004771
C00002660 External link 512 4-Methylcatechol
CHEMBL158766
C018599
1 / 2
C00002661 External link 512 Orcinol
CHEMBL110059
C005282
1 / 4 / 2
C00023720 External link 512 Toluquinol
CHEMBL450917
C062397
C00030878 External link 512 o-Cresol
CHEMBL46931
C034047
4 / 9 / 3 1 / 4
C00035128 External link 512 m-Cresol
/ m-Oxytoluene
CHEMBL298312
C042041
6 / 4 / 1 1 / 3

Human Protein / Gene in interactions

16 ChEMBL Protein in interactions

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

12 Gene in CTD interactions

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

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (20)

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 DISEASE (10)

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)

Diseases related to CTD interactions

13 disease in interactions with metabolites

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