Plant Species


Cumulative plant class count

class name count

Cumulative family count

class name count
Pseudomonadaceae 1

KEGG BRITE br08003 External link 512


Categories (0)

br08003 Category # of metabolite

metabolites link (0)

br08003 Category KEGG ID KNApSAcK ID

Metabolite list (1)

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
C00007533 External link 512 2-Aminophenol
CHEMBL28319
C027667
22 / 17 / 10 6 / 2

Human Protein / Gene in interactions

22 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P22310 UDP-glucuronosyltransferase 1-4 Enzyme C00007533 3 / 0
Q9HAW8 UDP-glucuronosyltransferase 1-10 Enzyme C00007533 0 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00007533 3 / 2
P16662 UDP-glucuronosyltransferase 2B7 Enzyme C00007533 0 / 0
Q9HAW7 UDP-glucuronosyltransferase 1-7 Enzyme C00007533 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00007533 2 / 0
O75496 Geminin Unclassified protein C00007533 0 / 0
P10145 Interleukin-8 Secreted protein C00007533 0 / 0
P11308 Transcriptional regulator ERG Unclassified protein C00007533 1 / 2
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00007533 5 / 3
Q96RI1 Bile acid receptor NR1H4 C00007533 0 / 0
P51449 Nuclear receptor ROR-gamma Nuclear hormone receptor subfamily 1 group F member 3 C00007533 0 / 0
P06133 UDP-glucuronosyltransferase 2B4 Enzyme C00007533 0 / 0
P36537 UDP-glucuronosyltransferase 2B10 Enzyme C00007533 0 / 0
Q9BY64 UDP-glucuronosyltransferase 2B28 Enzyme C00007533 0 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme C00007533 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00007533 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00007533 0 / 0
P10275 Androgen receptor NR3C4 C00007533 3 / 4
P35869 Aryl hydrocarbon receptor Transcription Factor C00007533 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00007533 1 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00007533 0 / 0

6 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
1646 AKR1C2, AKR1C-pseudo, BABP, DD, DD2, DDH2, HAKRD, HBAB, MCDR2, SRXY8 aldo-keto reductase family 1, member C2 (EC:1.3.1.20 1.1.1.357) C00007533
1543 CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) C00007533
3162 HMOX1, HMOX1D, HO-1, HSP32, bK286B10 heme oxygenase (decycling) 1 (EC:1.14.99.3) C00007533
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00007533
1728 NQO1, DHQU, DIA4, DTD, NMOR1, NMORI, QR1 NAD(P)H dehydrogenase, quinone 1 (EC:1.6.5.2) C00007533
10720 UGT2B11 UDP glucuronosyltransferase 2 family, polypeptide B11 (EC:2.4.1.17) C00007533

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (17)

OMIM preferred title UniProt
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
%606641 Body mass index; bmi P37231
#609338 Carotid intimal medial thickness 1 P37231
#114500 Colorectal cancer; crc P84022
#218800 Crigler-najjar syndrome, type i P22310
#606785 Crigler-najjar syndrome, type ii P22310
#612219 Ewing sarcoma; es P11308
#143500 Gilbert syndrome P22310
#137800 Glioma susceptibility 1; glm1 O75874
P37231
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#601665 Obesity P37231
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275

KEGG DISEASE (10)

KEGG name UniProt
H00024 Prostate cancer P10275 (related)
P11308 (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)
H00035 Ewing's sarcoma P11308 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H00032 Thyroid cancer P37231 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00420 Familial partial lipodystrophy (FPL) P37231 (related)

Diseases related to CTD interactions

2 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D006528 Carcinoma, Hepatocellular C00007533
D011230 Precancerous Conditions C00007533