Metabolite list (5)

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
C00002657 External link 512 p-Formylphenol
/ 4-Hydroxybenzaldehyde
/ p-Hydroxybenzaldehyde
CHEMBL14193
C011483
3 / 2 / 2
C00018099 External link 512 Catechaldehyde
/ Protocatechualdehyde
/ 3,4-Dihydroxybenzaldehyde
CHEMBL222021
C005581
7 / 0 / 0 5 / 2
C00029435 External link 512 2,4-Dihydroxybenzaldehyde
CHEMBL243587
2 / 0 / 0
C00029760 External link 512 Atranol
CHEMBL223288
C00031273 External link 512 Salicylaldehyde
CHEMBL108925
C013243
2 / 4 / 2

Human Protein / Gene in interactions

12 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00018099 C00029435 0 / 0
O00519 Fatty-acid amide hydrolase 1 Enzyme C00029435 C00031273 0 / 0
P80404 4-aminobutyrate aminotransferase, mitochondrial Transferase C00002657 1 / 1
P51151 Ras-related protein Rab-9A Unclassified protein C00018099 0 / 0
P51649 Succinate-semialdehyde dehydrogenase, mitochondrial Oxidoreductase C00002657 1 / 1
P14679 Tyrosinase Oxidoreductase C00031273 4 / 2
P14902 Indoleamine 2,3-dioxygenase 1 Enzyme C00002657 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00018099 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00018099 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00018099 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00018099 0 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00018099 0 / 0

5 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
177 AGER, RAGE advanced glycosylation end product-specific receptor C00018099
6285 S100B, NEF, S100, S100-B, S100beta S100 calcium binding protein B C00018099
4087 SMAD2, JV18, JV18-1, MADH2, MADR2, hMAD-2, hSMAD2 SMAD family member 2 C00018099
4088 SMAD3, HSPC193, HsT17436, JV15-2, LDS1C, LDS3, MADH3 SMAD family member 3 C00018099
7040 TGFB1, CED, DPD1, LAP, TGFB, TGFbeta transforming growth factor, beta 1 C00018099

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (6)

OMIM preferred title UniProt
#103470 Albinism, ocular, with sensorineural deafness P14679
#203100 Albinism, oculocutaneous, type ia; oca1a P14679
#606952 Albinism, oculocutaneous, type ib; oca1b P14679
#613163 Gaba-transaminase deficiency P80404
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679
#271980 Succinic semialdehyde dehydrogenase deficiency; ssadhd P51649

KEGG DISEASE (4)

KEGG name UniProt
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00038 Malignant melanoma P14679 (marker)
H00835 Succinic semialdehyde dehydrogenase (SSADH) deficiency P51649 (related)
H01257 GABA-transaminase deficiency P80404 (related)

Diseases related to CTD interactions

2 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D002386 Cataract C00018099
D048909 Diabetes Complications C00018099