Capparis leucophylla
Species
KNApSAcK Entry
| Organism name | Capparis leucophylla |
|---|---|
| Genus | Capparis |
| Family | Capparaceae |
| Kingdom | Plantae |
NCBI taxonomy
Entry
| Linked NCBI taxonomy name | Capparis |
|---|---|
| Linked NCBI taxonomy ID | 13394 |
| Linked level | genus |
Family
| Family in NCBI taxonomy | Capparaceae |
|---|---|
| ID | 301453 |
Kingdom (Superkingdom)
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
Plant class
| Plant class | rosids |
|---|---|
| ID | 71275 |
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 |
KCF-S
cluster |
phytochemical
cluster |
figure |
|---|---|---|---|---|---|---|---|---|
C00003672
|
Sitosterol
/ beta-sitosterl / (-)-beta-Sitosterol / Stigmast-5-en-3beta-ol |
CHEMBL221542
CHEMBL1398443 CHEMBL1875388 |
17 / 19 / 12 | No. 53 | No. 11 |
|
||
|
C00019308
|
Doursterol
/ Daucosterin / 3-O-beta-D-Glucopyranosyl sitosterol / beta-Sitosterol 3-O-beta-D-glucopyranoside |
CHEMBL197711
CHEMBL506678 CHEMBL2304043 |
C011015
|
5 / 4 / 2 | 0 / 3 | No. 520 |
|
|
|
C00002074
|
Stachydrine
|
CHEMBL394450
CHEMBL1456892 CHEMBL1986864 |
10 / 8 / 12 | No. 2627 | No. 1 |
|
||
|
C00007619
|
Citric acid
|
CHEMBL1261
|
D019343
|
101 / 48 / 38 | 15 / 7 | No. 7422 |
|
|
|
C00001198
|
Oxalic acid
|
CHEMBL146755
|
D019815
|
2 / 0 / 0 | 1 / 6 | No. 7540 |
|
Human Protein / Gene in interactions
116 ChEMBL Protein in interactions
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00002074 C00003672 C00007619 | 1 / 0 |
| P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00002074 C00003672 C00007619 | 0 / 1 |
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00002074 C00003672 C00007619 | 0 / 1 |
| P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00002074 C00003672 C00007619 | 0 / 0 |
| P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00002074 C00003672 C00007619 | 1 / 1 |
| P12931 | Proto-oncogene tyrosine-protein kinase Src | Src | C00001198 C00007619 | 0 / 0 |
| O94956 | Solute carrier organic anion transporter family member 2B1 | Unclassified protein | C00001198 C00007619 | 0 / 0 |
| P03372 | Estrogen receptor | NR3A1 | C00003672 C00007619 | 1 / 1 |
| P00734 | Prothrombin | S1A | C00003672 C00019308 | 4 / 2 |
| P49841 | Glycogen synthase kinase-3 beta | Gsk | C00003672 C00019308 | 0 / 0 |
| P18031 | Tyrosine-protein phosphatase non-receptor type 1 | Tyr | C00003672 C00019308 | 0 / 0 |
| P06746 | DNA polymerase beta | Enzyme | C00003672 C00019308 | 0 / 0 |
| P16473 | Thyrotropin receptor | Glycohormone receptor | C00002074 C00003672 | 3 / 2 |
| P08047 | Transcription factor Sp1 | Unclassified protein | C00003672 C00019308 | 0 / 0 |
| P25101 | Endothelin-1 receptor | Endothelin receptor | C00007619 | 0 / 0 |
| P27361 | Mitogen-activated protein kinase 3 | Erk | C00007619 | 0 / 0 |
| P14780 | Matrix metalloproteinase-9 | M10A | C00007619 | 2 / 2 |
| P41235 | Hepatocyte nuclear factor 4-alpha | Unclassified protein | C00007619 | 3 / 1 |
| P29466 | Caspase-1 | C14 | C00007619 | 0 / 0 |
| P49146 | Neuropeptide Y receptor type 2 | Neuropeptide Y receptor | C00007619 | 0 / 0 |
| P10828 | Thyroid hormone receptor beta | NR1A2 | C00007619 | 3 / 1 |
| P00918 | Carbonic anhydrase 2 | Lyase | C00007619 | 1 / 2 |
| P07550 | Beta-2 adrenergic receptor | Adrenergic receptor | C00007619 | 0 / 1 |
| P21397 | Amine oxidase [flavin-containing] A | Oxidoreductase | C00007619 | 1 / 1 |
| P25021 | Histamine H2 receptor | Histamine receptor | C00007619 | 0 / 0 |
| P35367 | Histamine H1 receptor | Histamine receptor | C00007619 | 0 / 0 |
| Q01959 | Sodium-dependent dopamine transporter | Dopamine | C00007619 | 1 / 0 |
| P08912 | Muscarinic acetylcholine receptor M5 | Acetylcholine receptor | C00007619 | 0 / 0 |
| P18825 | Alpha-2C adrenergic receptor | Adrenergic receptor | C00007619 | 0 / 0 |
| P13945 | Beta-3 adrenergic receptor | Adrenergic receptor | C00007619 | 0 / 0 |
| P08183 | Multidrug resistance protein 1 | drug | C00003672 | 1 / 0 |
| P25024 | C-X-C chemokine receptor type 1 | CXC chemokine receptor | C00007619 | 0 / 0 |
| P06241 | Tyrosine-protein kinase Fyn | Src | C00007619 | 0 / 0 |
| Q08209 | Serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform | Ser_Thr | C00007619 | 0 / 0 |
| Q16539 | Mitogen-activated protein kinase 14 | p38 | C00007619 | 0 / 0 |
| Q9GZT9 | Egl nine homolog 1 | Enzyme | C00007619 | 1 / 1 |
| P00533 | Epidermal growth factor receptor | TK tyrosine-protein kinase EGFR subfamily | C00007619 | 1 / 8 |
| P14416 | D(2) dopamine receptor | Dopamine receptor | C00007619 | 2 / 0 |
| P23219 | Prostaglandin G/H synthase 1 | Oxidoreductase | C00007619 | 0 / 0 |
| P37288 | Vasopressin V1a receptor | Vasopressin and oxytocin receptor | C00007619 | 0 / 0 |
| P41145 | Kappa-type opioid receptor | Opioid receptor | C00007619 | 0 / 0 |
| Q9Y271 | Cysteinyl leukotriene receptor 1 | Leukotriene receptor | C00007619 | 0 / 0 |
| P29274 | Adenosine receptor A2a | Adenosine receptor | C00007619 | 0 / 0 |
| P25929 | Neuropeptide Y receptor type 1 | Neuropeptide Y receptor | C00007619 | 0 / 0 |
| P50052 | Type-2 angiotensin II receptor | Angiotensin receptor | C00007619 | 1 / 1 |
| P17948 | Vascular endothelial growth factor receptor 1 | Vegfr | C00007619 | 0 / 0 |
| P41968 | Melanocortin receptor 3 | Melanocortin receptor | C00007619 | 1 / 0 |
| P00352 | Retinal dehydrogenase 1 | Enzyme | C00007619 | 0 / 0 |
| P11509 | Cytochrome P450 2A6 | Cytochrome P450 2A6 | C00007619 | 0 / 0 |
| Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00002074 | 0 / 0 |
| P04035 | 3-hydroxy-3-methylglutaryl-coenzyme A reductase | Oxidoreductase | C00007619 | 0 / 0 |
| P08913 | Alpha-2A adrenergic receptor | Adrenergic receptor | C00007619 | 0 / 0 |
| P21917 | D(4) dopamine receptor | Dopamine receptor | C00007619 | 0 / 0 |
| P30988 | Calcitonin receptor | Calcitonin receptor | C00007619 | 0 / 0 |
| P35462 | D(3) dopamine receptor | Dopamine receptor | C00007619 | 1 / 0 |
| P41143 | Delta-type opioid receptor | Opioid receptor | C00007619 | 0 / 0 |
| Q92731 | Estrogen receptor beta | NR3A2 | C00007619 | 0 / 1 |
| P41595 | 5-hydroxytryptamine receptor 2B | Serotonin receptor | C00007619 | 0 / 0 |
| P17252 | Protein kinase C alpha type | Alpha | C00007619 | 0 / 0 |
| P30411 | B2 bradykinin receptor | Bradykinin receptor | C00007619 | 0 / 0 |
| P32245 | Melanocortin receptor 4 | Melanocortin receptor | C00007619 | 1 / 0 |
| P33765 | Adenosine receptor A3 | Adenosine receptor | C00007619 | 0 / 0 |
| P32238 | Cholecystokinin receptor type A | Cholecystokinin receptor | C00007619 | 0 / 0 |
| P08311 | Cathepsin G | S1A | C00007619 | 0 / 0 |
| Q99720 | Sigma non-opioid intracellular receptor 1 | Membrane receptor | C00007619 | 1 / 0 |
| P03956 | Interstitial collagenase | M10A | C00007619 | 0 / 1 |
| P32241 | Vasoactive intestinal polypeptide receptor 1 | Vasoactive intestinal peptide receptor | C00007619 | 0 / 0 |
| O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00002074 | 0 / 0 |
| P08246 | Neutrophil elastase | S1A | C00007619 | 2 / 1 |
| P04150 | Glucocorticoid receptor | NR3C1 | C00007619 | 0 / 1 |
| P08172 | Muscarinic acetylcholine receptor M2 | Acetylcholine receptor | C00007619 | 2 / 0 |
| P11229 | Muscarinic acetylcholine receptor M1 | Acetylcholine receptor | C00007619 | 0 / 0 |
| P14679 | Tyrosinase | Oxidoreductase | C00003672 | 4 / 2 |
| P21554 | Cannabinoid receptor 1 | Cannabinoid receptor | C00007619 | 0 / 0 |
| P31645 | Sodium-dependent serotonin transporter | Serotonin | C00007619 | 2 / 0 |
| P37231 | Peroxisome proliferator-activated receptor gamma | NR1C3 | C00007619 | 5 / 3 |
| P04626 | Receptor tyrosine-protein kinase erbB-2 | TK tyrosine-protein kinase EGFR subfamily | C00007619 | 5 / 9 |
| P20309 | Muscarinic acetylcholine receptor M3 | Acetylcholine receptor | C00007619 | 1 / 0 |
| P21452 | Substance-K receptor | Neurokinin receptor | C00007619 | 0 / 0 |
| Q12809 | Potassium voltage-gated channel subfamily H member 2 | KCNH, Kv10-12.x (Ether-a-go-go) | C00007619 | 2 / 2 |
| P51679 | C-C chemokine receptor type 4 | CC chemokine receptor | C00007619 | 0 / 0 |
| P51681 | C-C chemokine receptor type 5 | CC chemokine receptor | C00007619 | 3 / 0 |
| P50406 | 5-hydroxytryptamine receptor 6 | Serotonin receptor | C00007619 | 0 / 0 |
| Q96RI1 | Bile acid receptor | NR1H4 | C00007619 | 0 / 0 |
| P41597 | C-C chemokine receptor type 2 | CC chemokine receptor | C00007619 | 1 / 0 |
| P28482 | Mitogen-activated protein kinase 1 | Erk | C00007619 | 0 / 0 |
| P08575 | Receptor-type tyrosine-protein phosphatase C | Enzyme | C00007619 | 2 / 1 |
| P35354 | Prostaglandin G/H synthase 2 | Oxidoreductase | C00007619 | 0 / 3 |
| O76074 | cGMP-specific 3',5'-cyclic phosphodiesterase | PDE_5A | C00007619 | 0 / 0 |
| P21728 | D(1A) dopamine receptor | Dopamine receptor | C00007619 | 0 / 0 |
| P08588 | Beta-1 adrenergic receptor | Adrenergic receptor | C00007619 | 1 / 0 |
| P22303 | Acetylcholinesterase | Hydrolase | C00007619 | 1 / 0 |
| P28223 | 5-hydroxytryptamine receptor 2A | Serotonin receptor | C00007619 | 0 / 0 |
| P28335 | 5-hydroxytryptamine receptor 2C | Serotonin receptor | C00007619 | 0 / 0 |
| P35372 | Mu-type opioid receptor | Opioid receptor | C00007619 | 0 / 0 |
| P08173 | Muscarinic acetylcholine receptor M4 | Acetylcholine receptor | C00007619 | 0 / 0 |
| P25103 | Substance-P receptor | Neurokinin receptor | C00007619 | 0 / 0 |
| P25105 | Platelet-activating factor receptor | PAF receptor | C00007619 | 0 / 0 |
| P33032 | Melanocortin receptor 5 | Melanocortin receptor | C00007619 | 0 / 0 |
| P49798 | Regulator of G-protein signaling 4 | Unclassified protein | C00003672 | 2 / 0 |
| O60240 | Perilipin-1 | Unclassified protein | C00007619 | 1 / 0 |
| P05181 | Cytochrome P450 2E1 | Cytochrome P450 2E1 | C00007619 | 0 / 0 |
| O75164 | Lysine-specific demethylase 4A | Enzyme | C00007619 | 0 / 0 |
| Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00007619 | 0 / 0 |
| P23975 | Sodium-dependent noradrenaline transporter | Norepinephrine | C00007619 | 1 / 1 |
| P25100 | Alpha-1D adrenergic receptor | Adrenergic receptor | C00007619 | 0 / 0 |
| P30542 | Adenosine receptor A1 | Adenosine receptor | C00007619 | 0 / 0 |
| P18089 | Alpha-2B adrenergic receptor | Adrenergic receptor | C00007619 | 0 / 0 |
| P24557 | Thromboxane-A synthase | Cytochrome P450 5A1 | C00007619 | 1 / 1 |
| P06239 | Tyrosine-protein kinase Lck | Src | C00007619 | 0 / 1 |
| P25025 | C-X-C chemokine receptor type 2 | CXC chemokine receptor | C00007619 | 0 / 0 |
| P80365 | Corticosteroid 11-beta-dehydrogenase isozyme 2 | Enzyme | C00003672 | 1 / 1 |
| Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00003672 | 1 / 1 |
| O00255 | Menin | Unclassified protein | C00002074 | 2 / 5 |
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00002074 | 1 / 2 |
| Q9C0B1 | Alpha-ketoglutarate-dependent dioxygenase FTO | Unclassified protein | C00007619 | 1 / 2 |
16 Gene in CTD interactions
| gene | gene name | gene description | KNApSAcK metabolite in interactions |
|---|---|---|---|
| 50 | ACO2, ACONM, ICRD | aconitase 2, mitochondrial (EC:4.2.1.3) |
C00007619
|
| 581 | BAX, BCL2L4 | BCL2-associated X protein |
C00007619
|
| 596 | BCL2, Bcl-2, PPP1R50 | B-cell CLL/lymphoma 2 |
C00007619
|
| 598 | BCL2L1, BCL-XL/S, BCL2L, BCLX, BCLXL, BCLXS, Bcl-X, PPP1R52, bcl-xL, bcl-xS | BCL2-like 1 |
C00007619
|
| 100506742 | CASP12, CASP-12, CASP12P1 | caspase 12 (gene/pseudogene) |
C00007619
|
| 836 | CASP3, CPP32, CPP32B, SCA-1 | caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) |
C00007619
|
| 1026 | CDKN1A, CAP20, CDKN1, CIP1, MDA-6, P21, SDI1, WAF1, p21CIP1 | cyclin-dependent kinase inhibitor 1A (p21, Cip1) |
C00007619
|
| 2746 | GLUD1, GDH, GDH1, GLUD | glutamate dehydrogenase 1 (EC:1.4.1.3) |
C00007619
|
| 25818 | KLK5, KLK-L2, KLKL2, SCTE | kallikrein-related peptidase 5 |
C00007619
|
| 4586 | MUC5AC, MUC5, TBM, leB | mucin 5AC, oligomeric mucus/gel-forming |
C00007619
|
| 9058 | SLC13A2, NADC1, NaCT, NaDC-1, SDCT1 | solute carrier family 13 (sodium-dependent dicarboxylate transporter), member 2 |
C00007619
|
| 7015 | TERT, CMM9, DKCA2, DKCB4, EST2, PFBMFT1, TCS1, TP2, TRT, hEST2, hTRT | telomerase reverse transcriptase (EC:2.7.7.49) |
C00007619
|
| 7018 | TF, PRO1557, PRO2086, TFQTL1 | transferrin |
C00007619
|
| 7442 | TRPV1, VR1 | transient receptor potential cation channel, subfamily V, member 1 |
C00007619
|
| 7422 | VEGFA, MVCD1, VEGF, VPF | vascular endothelial growth factor A |
C00007619
|
| 26762 | HAVCR1, HAVCR, HAVCR-1, KIM-1, KIM1, TIM, TIM-1, TIM1, TIMD-1, TIMD1 | hepatitis A virus cellular receptor 1 |
C00001198
|
Related Diseases
Diseases related to proteins in ChEMBL interactions
OMIM (67)
| OMIM | preferred title | UniProt |
|---|---|---|
| #100100 | Abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism |
P20309
|
| #103470 | Albinism, ocular, with sensorineural deafness |
P14679
|
| #203100 | Albinism, oculocutaneous, type ia; oca1a |
P14679
|
| #606952 | Albinism, oculocutaneous, type ib; oca1b |
P14679
|
| #103780 | Alcohol dependence |
P08172
P14416 P31645 |
| #614373 | Amyotrophic lateral sclerosis 16, juvenile; als16 |
Q99720
|
| #218030 | Apparent mineralocorticoid excess; ame |
P80365
|
| #602025 | Body mass index quantitative trait locus 9; bmiq9 |
P41968
|
| %606641 | Body mass index; bmi |
P37231
|
| #300615 | Brunner syndrome |
P21397
|
| #609338 | Carotid intimal medial thickness 1 |
P37231
|
| #162800 | Cyclic neutropenia |
P08246
|
| #612522 | Diabetes mellitus, insulin-dependent, 22; iddm22 |
P51681
|
| #125853 | Diabetes mellitus, noninsulin-dependent; niddm |
P41235
|
| #609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
| #608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
| #609820 | Erythrocytosis, familial, 3; ecyt3 |
Q9GZT9
|
| #615363 | Estrogen resistance; estrr |
P03372
|
| #613659 | Gastric cancer |
P04626
|
| #137215 | Gastric cancer, hereditary diffuse; hdgc |
P04626
|
| #231095 | Ghosal hematodiaphyseal dysplasia; ghdd |
P24557
|
| #137800 | Glioma susceptibility 1; glm1 |
P04626
P37231 |
| #612938 | Growth retardation, developmental delay, coarse facies, and early death; gdfd |
Q9C0B1
|
| #605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
| #609423 | Human immunodeficiency virus type 1, susceptibility to |
P41597
P51681 |
| #145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
| #603373 | Hyperthyroidism, familial gestational |
P16473
|
| #609152 | Hyperthyroidism, nonautoimmune |
P16473
|
| #275200 | Hypothyroidism, congenital, nongoitrous, 1; chng1 |
P16473
|
| #612244 | Inflammatory bowel disease 13; ibd13 |
P08183
|
| #603932 | Intervertebral disc disease; idd |
P14780
|
| #604367 | Lipodystrophy, familial partial, type 3; fpld3 |
P37231
|
| #613877 | Lipodystrophy, familial partial, type 4; fpld4 |
O60240
|
| #613688 | Long qt syndrome 2; lqt2 |
Q12809
|
| #211980 | Lung cancer |
P00533
P04626 |
| #608516 | Major depressive disorder; mdd |
P08172
|
| #125850 | Maturity-onset diabetes of the young, type 1; mody1 |
P41235
|
| #606391 | Maturity-onset diabetes of the young; mody |
P41235
|
| %300852 | Mental retardation, x-linked 88; mrx88 |
P50052
|
| #613073 | Metaphyseal anadysplasia 2; mandp2 |
P14780
|
| #131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
| #126200 | Multiple sclerosis, susceptibility to; ms |
P08575
|
| #159900 | Myoclonic dystonia |
P14416
|
| #202700 | Neutropenia, severe congenital, 1, autosomal dominant; scn1 |
P08246
|
| #601665 | Obesity |
P32245
P37231 |
| #164230 | Obsessive-compulsive disorder; ocd |
P31645
|
| #604715 | Orthostatic intolerance |
P23975
|
| #259730 | Osteopetrosis, autosomal recessive 3; optb3 |
P00918
|
| #167000 | Ovarian cancer |
P04626
|
| #613135 | Parkinsonism-dystonia, infantile; pkdys |
Q01959
|
| #614390 | Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 |
P00734
|
| #613679 | Prothrombin deficiency, congenital |
P00734
|
| #607276 | Resting heart rate, variation in |
P08588
|
| #604906 | Schizophrenia 9; sczd9 |
P49798
|
| #181500 | Schizophrenia; sczd |
P49798
|
| #608971 | Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-positive |
P08575
|
| #609620 | Short qt syndrome 1; sqt1 |
Q12809
|
| #601800 | Skin/hair/eye pigmentation, variation in, 3; shep3 |
P14679
|
| #607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
| #601367 | Stroke, ischemic |
P00734
|
| #188050 | Thrombophilia due to thrombin defect; thph1 |
P00734
|
| #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
|
| #190300 | Tremor, hereditary essential, 1; etm1 |
P35462
|
| #610379 | West nile virus, susceptibility to |
P51681
|
| #112100 | Yt blood group antigen |
P22303
|
KEGG DISEASE (53)
| KEGG | name | UniProt |
|---|---|---|
| H00033 | Adrenal carcinoma |
O00255
(related)
|
| H00034 | Carcinoid |
O00255
(related)
|
| H00045 | Malignant islet cell carcinoma |
O00255
(related)
|
| H00246 | Primary hyperparathyroidism |
O00255
(related)
|
| H01102 | Pituitary adenomas |
O00255
(related)
|
| H00016 | Oral cancer |
P00533
(related)
P00533 (marker) |
| H00017 | Esophageal cancer |
P00533
(related)
P35354 (related) |
| H00018 | Gastric cancer |
P00533
(related)
P04626 (related) |
| H00022 | Bladder cancer |
P00533
(related)
P04626 (related) |
| H00028 | Choriocarcinoma |
P00533
(related)
P03956 (related) P04626 (related) |
| H00030 | Cervical cancer |
P00533
(related)
P04626 (related) |
| H00042 | Glioma |
P00533
(related)
P00533 (marker) |
| H00055 | Laryngeal cancer |
P00533
(related)
P00533 (marker) |
| H00223 | Inherited thrombophilia |
P00734
(related)
|
| H01254 | Congenital prothrombin deficiency |
P00734
(related)
|
| H00241 | Combined proximal and distal renal tubular acidosis (RTA type 3) |
P00918
(related)
|
| H00436 | Osteopetrosis |
P00918
(related)
|
| H00026 | Endometrial Cancer |
P03372
(marker)
P04626 (related) Q92731 (marker) |
| H00599 | 46,XX disorders of sex development (Disorders related to androgen excess) |
P04150
(related)
|
| H00019 | Pancreatic cancer |
P04626
(related)
|
| H00027 | Ovarian cancer |
P04626
(related)
|
| H00031 | Breast cancer |
P04626
(related)
P04626 (marker) |
| H00046 | Cholangiocarcinoma |
P04626
(related)
P35354 (related) |
| H00093 | Combined immunodeficiencies (CIDs) |
P06239
(related)
|
| H00079 | Asthma |
P07550
(related)
|
| H00100 | Neutropenic disorders |
P08246
(related)
|
| H00091 | T-B+Severe combined immunodeficiencies (SCIDs) |
P08575
(related)
|
| H00036 | Osteosarcoma |
P08684
(marker)
|
| H00249 | Thyroid hormone resistance syndrome |
P10828
(related)
|
| H01205 | Coumarin resistance |
P11712
(related)
|
| H00168 | Oculocutaneous albinism (OCA) |
P14679
(related)
|
| H00038 | Malignant melanoma |
P14679
(marker)
|
| H00025 | Penile cancer |
P14780
(related)
P35354 (related) |
| H00479 | Metaphyseal dysplasias |
P14780
(related)
|
| H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P16473
(related)
|
| H01269 | Congenital hyperthyroidism |
P16473
(related)
|
| H00548 | Brunner syndrome |
P21397
(related)
|
| H01031 | Orthostatic intolerance (OI) |
P23975
(related)
|
| H00490 | Diaphyseal dysplasia with anemia (Ghosal) |
P24557
(related)
|
| H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
| H00032 | Thyroid cancer |
P37231
(related)
|
| H00409 | Type II diabetes mellitus |
P37231
(related)
Q9C0B1 (related) |
| H00420 | Familial partial lipodystrophy (FPL) |
P37231
(related)
|
| H00410 | Maturity onset diabetes of the young (MODY) |
P41235
(related)
|
| H00480 | Non-syndromic X-linked mental retardation |
P50052
(related)
|
| H00259 | Apparent mineralocorticoid excess syndrome |
P80365
(related)
|
| H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q03164
(related)
Q03164 (marker) |
| H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) |
Q03164
(related)
|
| H00720 | Long QT syndrome |
Q12809
(related)
|
| H00725 | Short QT syndrome |
Q12809
(related)
|
| H00926 | Growth retardation, developmental delay, coarse facies, and early death |
Q9C0B1
(related)
|
| H00236 | Congenital polycythemia |
Q9GZT9
(related)
|
| H00063 | Spinocerebellar ataxia (SCA) |
Q9NUW8
(related)
|
Diseases related to CTD interactions
16 disease in interactions with metabolites
| MESH or OMIM | name |
KNApSAcK
metabolite |
|---|---|---|
| D002493 | Central Nervous System Diseases |
C00019308
|
| D003072 | Cognition Disorders |
C00019308
|
| D013118 | Spinal Cord Diseases |
C00019308
|
| D002418 | Cattle Diseases |
C00007619
|
| D003371 | Cough |
C00007619
|
| D004716 | Endometritis |
C00007619
|
| D017202 | Myocardial Ischemia |
C00007619
|
| D011645 | Puerperal Infection |
C00007619
|
| D053201 | Urinary Bladder, Overactive |
C00007619
|
| D014652 | Vascular Diseases |
C00007619
|
| D058186 | Acute Kidney Injury |
C00001198
|
| D006959 | Hyperoxaluria |
C00001198
|
| D006960 | Hyperoxaluria, Primary |
C00001198
|
| D009397 | Nephrocalcinosis |
C00001198
|
| D053040 | Nephrolithiasis |
C00001198
|
| D051437 | Renal Insufficiency |
C00001198
|