Metabolite list (30)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
KCF-S
cluster
figure
C00003106 External link 512 gamma-Muurolene
/ 1beta-Cadina-4,10(15)-diene
No. 283
C00035828 External link 512 1(10),4-Cadinadiene-3,9-diol
/ 3,9-Dihydroxy-delta-cadinene
No. 283
C00035520 External link 512 Cadina-1(10),4-dien
No. 283
C00020041 External link 512 gamma-Bulgarene
No. 283
C00020042 External link 512 (-)-Khusol
/ Cadina-4,10(15)-dien-12-ol
No. 283
C00020044 External link 512 Khusinol
/ 1beta,6alpha,7betaH-Cadina-4,10(15)-dien-2beta-ol
No. 283
C00030434 External link 512 omega-Cadinene
/ 1(10),3-Cadinadiene
No. 283
C00020049 External link 512 gamma1-Cadinene
No. 283
C00020051 External link 512 (-)-epsilon-Bulgarene
No. 283
C00020052 External link 512 10beta,15-Epoxykhusinol
/ 1beta,6alpha,7betaH-Cadina-4,10(15)-dien-3alpha-ol
No. 283
C00030345 External link 512 14-Hydroxy-delta-cadinene
No. 283
C00029866 External link 512 delta-Cadinene
CHEMBL445759
No. 283
C00020057 External link 512 alpha-Amorphene
No. 283
C00020058 External link 512 alpha-Muurolene
No. 283
C00020059 External link 512 alpha-Cadinene
No. 283
C00029671 External link 512 delta-Amorphene
/ (+)-delta-Amorphene
CHEMBL445759
No. 283
C00020130 External link 512 Sclerosporal
/ 14-Oxy-alpha-muurolene
No. 283
C00020249 External link 512 Cubenene
/ Cadina-1,4-diene
/ Cadina-1(2),4-diene
No. 283
C00020384 External link 512 6,9-Guaiadiene
No. 283
C00020128 External link 512 beta-Cadinene
No. 283
C00029396 External link 512 Guaia-6,9-diene
/ (+)-Guaia-6,9-diene
No. 1524
C00020056 External link 512 beta1-Bulgarene
/ 4,9-Bulgaradiene
No. 1524
C00020053 External link 512 4,10(14)-Oplopadien-3-ol
No. 1524
C00020048 External link 512 gamma2-Cadinene
/ 3,10(14)-Cadinadiene
No. 1524
C00035061 External link 512 delta-Cadinen-9-one
/ 1(10),4-Cadinadien-9-one
No. 1524
C00037022 External link 512 (R)-(-)-Gossypol
CHEMBL51483
78 / 69 / 87 No. 1524
C00007636 External link 512 gamma-Cadinene
C054278
No. 1524
C00003136 External link 512 gamma-Amorphene
/ (+)-gamma-Amorphene
No. 4111
C00038078 External link 512 Gossypol
CHEMBL51483
D006072
78 / 69 / 87 17 / 2 No. 4111
C00038103 External link 512 (+)-Gossypol
CHEMBL51483
78 / 69 / 87 No. 4111

Human Protein / Gene in interactions

78 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00003136 C00038078 C00038103 1 / 0
P42345 Serine/threonine-protein kinase mTOR Enzyme C00003136 C00038078 C00038103 0 / 0
P14061 Estradiol 17-beta-dehydrogenase 1 Enzyme C00003136 C00038078 C00038103 0 / 0
P04637 Cellular tumor antigen p53 Transcription Factor C00003136 C00038078 C00038103 7 / 37
Q07820 Induced myeloid leukemia cell differentiation protein Mcl-1 Other cytosolic protein C00003136 C00038078 C00038103 0 / 0
Q16637 Survival motor neuron protein Unclassified protein C00003136 C00038078 C00038103 4 / 1
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00003136 C00038078 C00038103 0 / 0
Q99700 Ataxin-2 Unclassified protein C00003136 C00038078 C00038103 1 / 1
P49798 Regulator of G-protein signaling 4 Unclassified protein C00003136 C00038078 C00038103 2 / 0
P21728 D(1A) dopamine receptor Dopamine receptor C00003136 C00038078 C00038103 0 / 0
P06746 DNA polymerase beta Enzyme C00003136 C00038078 C00038103 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00003136 C00038078 C00038103 1 / 1
P29466 Caspase-1 C14 C00003136 C00038078 C00038103 0 / 0
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 C00003136 C00038078 C00038103 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00003136 C00038078 C00038103 0 / 0
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00003136 C00038078 C00038103 0 / 0
P02545 Prelamin-A/C Unclassified protein C00003136 C00038078 C00038103 11 / 10
P37840 Alpha-synuclein Unclassified protein C00003136 C00038078 C00038103 4 / 2
P10828 Thyroid hormone receptor beta NR1A2 C00003136 C00038078 C00038103 3 / 1
P19793 Retinoic acid receptor RXR-alpha NR2B1 C00003136 C00038078 C00038103 0 / 0
P02768 Serum albumin Secreted protein C00003136 C00038078 C00038103 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00003136 C00038078 C00038103 0 / 1
Q92843 Bcl-2-like protein 2 Other cytosolic protein C00003136 C00038078 C00038103 0 / 0
P54132 Bloom syndrome protein Enzyme C00003136 C00038078 C00038103 1 / 2
P51570 Galactokinase Enzyme C00003136 C00038078 C00038103 1 / 1
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00003136 C00038078 C00038103 1 / 0
P11473 Vitamin D3 receptor NR1I1 C00003136 C00038078 C00038103 2 / 3
O15296 Arachidonate 15-lipoxygenase B Enzyme C00003136 C00038078 C00038103 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00003136 C00038078 C00038103 0 / 0
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00003136 C00038078 C00038103 0 / 0
P39748 Flap endonuclease 1 Enzyme C00003136 C00038078 C00038103 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00003136 C00038078 C00038103 0 / 0
P42858 Huntingtin Unclassified protein C00003136 C00038078 C00038103 1 / 1
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00003136 C00038078 C00038103 2 / 0
O75496 Geminin Unclassified protein C00003136 C00038078 C00038103 0 / 0
P51151 Ras-related protein Rab-9A Unclassified protein C00003136 C00038078 C00038103 0 / 0
P15121 Aldose reductase Enzyme C00003136 C00038078 C00038103 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00003136 C00038078 C00038103 0 / 0
P11021 78 kDa glucose-regulated protein Unclassified protein C00003136 C00038078 C00038103 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00003136 C00038078 C00038103 0 / 0
P04150 Glucocorticoid receptor NR3C1 C00003136 C00038078 C00038103 0 / 1
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00003136 C00038078 C00038103 5 / 3
P18054 Arachidonate 12-lipoxygenase, 12S-type Enzyme C00003136 C00038078 C00038103 2 / 0
Q96RI1 Bile acid receptor NR1H4 C00003136 C00038078 C00038103 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00003136 C00038078 C00038103 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00003136 C00038078 C00038103 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00003136 C00038078 C00038103 3 / 3
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00003136 C00038078 C00038103 2 / 2
O15118 Niemann-Pick C1 protein Unclassified protein C00003136 C00038078 C00038103 1 / 1
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00003136 C00038078 C00038103 0 / 0
P03372 Estrogen receptor NR3A1 C00003136 C00038078 C00038103 1 / 1
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor C00003136 C00038078 C00038103 0 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme C00003136 C00038078 C00038103 0 / 0
P55210 Caspase-7 C14 C00003136 C00038078 C00038103 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00003136 C00038078 C00038103 1 / 1
P37059 Estradiol 17-beta-dehydrogenase 2 Enzyme C00003136 C00038078 C00038103 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00003136 C00038078 C00038103 0 / 1
P52732 Kinesin-like protein KIF11 Other cytosolic protein C00003136 C00038078 C00038103 1 / 0
Q9UNA4 DNA polymerase iota Enzyme C00003136 C00038078 C00038103 0 / 0
Q6W5P4 Neuropeptide S receptor Neuropeptide receptor C00003136 C00038078 C00038103 1 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00003136 C00038078 C00038103 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00003136 C00038078 C00038103 4 / 3
Q99549 M-phase phosphoprotein 8 Unclassified protein C00003136 C00038078 C00038103 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00003136 C00038078 C00038103 0 / 0
P10275 Androgen receptor NR3C4 C00003136 C00038078 C00038103 3 / 4
Q07869 Peroxisome proliferator-activated receptor alpha NR1C1 C00003136 C00038078 C00038103 0 / 0
Q07817 Bcl-2-like protein 1 Other cytosolic protein C00003136 C00038078 C00038103 0 / 0
P10415 Apoptosis regulator Bcl-2 Other cytosolic protein C00003136 C00038078 C00038103 0 / 7
Q9UBT6 DNA polymerase kappa Enzyme C00003136 C00038078 C00038103 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00003136 C00038078 C00038103 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00003136 C00038078 C00038103 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00003136 C00038078 C00038103 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00003136 C00038078 C00038103 1 / 1
O00255 Menin Unclassified protein C00003136 C00038078 C00038103 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00003136 C00038078 C00038103 1 / 2
Q13951 Core-binding factor subunit beta Unclassified protein C00003136 C00038078 C00038103 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00003136 C00038078 C00038103 1 / 4
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00003136 C00038078 C00038103 0 / 0

17 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
27113 BBC3, JFY-1, JFY1, PUMA BCL2 binding component 3 C00003136
598 BCL2L1, BCL-XL/S, BCL2L, BCLX, BCLXL, BCLXS, Bcl-X, PPP1R52, bcl-xL, bcl-xS BCL2-like 1 C00003136
10018 BCL2L11, BAM, BIM, BOD BCL2-like 11 (apoptosis facilitator) C00003136
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00003136
840 CASP7, CASP-7, CMH-1, ICE-LAP3, LICE2, MCH3 caspase 7, apoptosis-related cysteine peptidase (EC:3.4.22.60) C00003136
842 CASP9, APAF-3, APAF3, ICE-LAP6, MCH6, PPP1R56 caspase 9, apoptosis-related cysteine peptidase (EC:3.4.22.62) C00003136
6347 CCL2, GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1, SCYA2, SMC-CF chemokine (C-C motif) ligand 2 C00003136
2919 CXCL1, FSP, GRO1, GROa, MGSA, MGSA-a, NAP-3, SCYB1 chemokine (C-X-C motif) ligand 1 (melanoma growth stimulating activity, alpha) C00003136
2050 EPHB4, HTK, MYK1, TYRO11 EPH receptor B4 (EC:2.7.10.1) C00003136
2247 FGF2, BFGF, FGF-2, FGFB, HBGF-2 fibroblast growth factor 2 (basic) C00003136
2261 FGFR3, ACH, CD333, CEK2, HSFGFR3EX, JTK4 fibroblast growth factor receptor 3 (EC:2.7.10.1) C00003136
3397 ID1, ID, bHLHb24 inhibitor of DNA binding 1, dominant negative helix-loop-helix protein C00003136
3911 LAMA5 laminin, alpha 5 C00003136
4170 MCL1, BCL2L3, EAT, MCL1-ES, MCL1L, MCL1S, Mcl-1, TM, bcl2-L-3, mcl1/EAT myeloid cell leukemia sequence 1 (BCL2-related) C00003136
4192 MDK, ARAP, MK, NEGF2 midkine (neurite growth-promoting factor 2) C00003136
5154 PDGFA, PDGF-A, PDGF1 platelet-derived growth factor alpha polypeptide C00003136
1890 TYMP, ECGF, ECGF1, MEDPS1, MNGIE, MTDPS1, PDECGF, TP, hPD-ECGF thymidine phosphorylase (EC:2.4.2.4) C00003136

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (69)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#608584 Asthma-related traits, susceptibility to, 2 Q6W5P4
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#210900 Bloom syndrome; blm P54132
%606641 Body mass index; bmi P37231
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#609338 Carotid intimal medial thickness 1 P37231
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#114500 Colorectal cancer; crc P18054
P84022
#127750 Dementia, lewy body; dlb P37840
#119900 Digital clubbing, isolated congenital P15428
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#133239 Esophageal cancer P04637
P18054
#615363 Estrogen resistance; estrr P03372
#600274 Frontotemporal dementia; ftd P10636
#230200 Galactokinase deficiency P51570
#137800 Glioma susceptibility 1; glm1 P37231
#232300 Glycogen storage disease ii P10253
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610140 Heart-hand syndrome, slovenian type P02545
#143100 Huntington disease; hd P42858
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#145000 Hyperparathyroidism 1; hrpt1 O00255
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#211980 Lung cancer P04637
#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
#152950 Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation; mclmr P52732
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#257220 Niemann-pick disease, type c1; npc1 O15118
#601665 Obesity P37231
#260500 Papilloma of choroid plexus; cpp P04637
#168601 Parkinson disease 1, autosomal dominant; park1 P37840
#605543 Parkinson disease 4, autosomal dominant; park4 P37840
#168600 Parkinson disease, late-onset; pd P37840
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#275210 Restrictive dermopathy, lethal P02545
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#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
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#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
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (87)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
P04637 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H00136 Niemann-Pick disease type C (NPC) O15118 (related)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
P37231 (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)
P04637 (related)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
H00004 Chronic myeloid leukemia (CML) P04637 (related)
Q01196 (related)
H00005 Chronic lymphocytic leukemia (CLL) P04637 (related)
P10415 (related)
H00006 Hairy-cell leukemia P04637 (related)
H00008 Burkitt lymphoma P04637 (related)
H00009 Adult T-cell leukemia P04637 (related)
H00010 Multiple myeloma P04637 (related)
H00013 Small cell lung cancer P04637 (related)
P10415 (related)
H00014 Non-small cell lung cancer P04637 (related)
H00015 Malignant pleural mesothelioma P04637 (related)
H00016 Oral cancer P04637 (related)
P04637 (marker)
H00017 Esophageal cancer P04637 (related)
P04637 (marker)
H00018 Gastric cancer P04637 (related)
P10415 (related)
H00019 Pancreatic cancer P04637 (related)
P04637 (marker)
H00020 Colorectal cancer P04637 (related)
P04637 (marker)
H00022 Bladder cancer P04637 (related)
H00025 Penile cancer P04637 (related)
P04637 (marker)
H00027 Ovarian cancer P04637 (related)
H00028 Choriocarcinoma P04637 (related)
P10415 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
H00032 Thyroid cancer P04637 (related)
P37231 (related)
H00036 Osteosarcoma P04637 (related)
P08684 (marker)
H00038 Malignant melanoma P04637 (related)
H00039 Basal cell carcinoma P04637 (related)
H00040 Squamous cell carcinoma P04637 (related)
H00041 Kaposi's sarcoma P04637 (related)
P10415 (related)
H00042 Glioma P04637 (related)
P04637 (marker)
H00044 Cancer of the anal canal P04637 (related)
H00046 Cholangiocarcinoma P04637 (related)
H00047 Gallbladder cancer P04637 (related)
H00048 Hepatocellular carcinoma P04637 (related)
H00055 Laryngeal cancer P04637 (related)
P04637 (marker)
H00881 Li-Fraumeni syndrome P04637 (related)
H01007 Choroid plexus papilloma P04637 (related)
H00021 Renal cell carcinoma P04637 (marker)
H00069 Glycogen storage diseases (GSD) P10253 (related)
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)
H00030 Cervical cancer P10415 (related)
H00054 Nasopharyngeal cancer P10415 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H01205 Coumarin resistance P11712 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00057 Parkinson's disease (PD) P37840 (related)
H00066 Lewy body dementia (LBD) P37840 (related)
H00059 Huntington's disease (HD) P42858 (related)
H00070 Galactosemia P51570 (related)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
Q03164 (related)
Q03164 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (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)

Diseases related to CTD interactions

2 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D004487 Edema C00003136
D007248 Infertility, Male C00003136