Species

KNApSAcK Entry

Organism name Engelhardia roxburghiana
Genus Engelhardia
Family Juglandaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Alfaropsis roxburghiana
Linked NCBI taxonomy ID 139932
Linked level species

Family

Family in NCBI taxonomy Juglandaceae
ID 16714

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (23)

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
C00034390 External link 512 3-epi-Betulinic acid
CHEMBL269277
CHEMBL71690
CHEMBL519059
CHEMBL1318530
CHEMBL2005635
34 / 17 / 14 No. 23 No. 51
C00029821 External link 512 Sitostenone
/ beta-Sitostenone
/ Stigmast-4-en-3-one
/ Stigmast-4-ene-3-one
CHEMBL66926
No. 53 No. 11
C00034729 External link 512 Tricosyl trans-ferulate
/ n-Tricosyl trans-ferulate
No. 447
C00034722 External link 512 Tetracosyl trans-ferulate
No. 447
C00034535 External link 512 Hexacosyl trans-ferulate
/ n-Hexacosyl trans-ferulate
No. 447
C00034485 External link 512 Docosyl trans-ferulate
No. 447
C00029961 External link 512 Cinnamic acid
/ .beta-Phenylacrylic acid
CHEMBL27246
C029010
5 / 2 / 2 16 / 2 No. 904 No. 6
C00029515 External link 512 p-Tyrosol
/ 4-(2-Hydroxyethyl)phenol
/ p-Hydroxyphenethyl alcohol
/ 2-(4-Hydroxyphenyl)ethanol
CHEMBL53566
C011867
6 / 3 / 5 No. 936 No. 6
C00002683 External link 512 Vanillin
CHEMBL13883
18 / 8 / 9 No. 1003
C00002682 External link 512 Vanillic acid
/ 3-Methoxy-4-hydroxybenzoic acid
CHEMBL120568
D014641
5 / 3 / 3 5 / 0 No. 1073
C00029476 External link 512 Eudesmic acid
/ Trimethylgallic acid
/ 3,4,5-Trimethoxybenzoic acid
CHEMBL377172
C005854
3 / 2 / 2 No. 1073
C00002689 External link 512 Apocynin
/ Acetovanillone
CHEMBL346919
C056165
2 / 0 / 0 43 / 10 No. 1494
C00034498 External link 512 Engelhardic acid
No. 2025
C00002657 External link 512 p-Formylphenol
/ 4-Hydroxybenzaldehyde
/ p-Hydroxybenzaldehyde
CHEMBL14193
C011483
3 / 2 / 2 No. 2076
C00000258 External link 512 2,6-Dimethoxy-p-benzoquinone
CHEMBL448515
C030511
22 / 32 / 55 No. 2517
C00034398 External link 512 5-Methoxy-1-naphthalenol
No. 3508
C00034374 External link 512 1-Methoxynaphthalene
No. 3508
C00034393 External link 512 4-(2-Hydroxyphenyl)-4-oxobutyric acid
No. 3936
C00034500 External link 512 Engelharquinone
/ (-)-Engelharquinone
CHEMBL2204406
No. 4494
C00034397 External link 512 5,8-Dihydroxy-4-methoxy-1-tetralone
No. 4978
C00034602 External link 512 Methyl-4-(butyryloxy)benzoate
No. 5786
C00034499 External link 512 Engelharolide
/ (+)-Engelharolide
No. 5958
C00034501 External link 512 Engelharquinone epoxide
No. 7996

Human Protein / Gene in interactions

80 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
O75496 Geminin Unclassified protein C00000258 C00002689 C00029476 C00034390 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00000258 C00002689 C00029476 0 / 0
P15121 Aldose reductase Enzyme C00002682 C00029961 C00034390 0 / 0
Q96RI1 Bile acid receptor NR1H4 C00002683 C00034390 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00000258 C00002682 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000258 C00034390 0 / 1
P03372 Estrogen receptor NR3A1 C00002682 C00029961 1 / 1
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00000258 C00002683 0 / 0
P80404 4-aminobutyrate aminotransferase, mitochondrial Transferase C00002657 C00002683 1 / 1
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00000258 C00034390 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00000258 C00034390 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00000258 C00034390 1 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00002683 C00029515 0 / 0
P51649 Succinate-semialdehyde dehydrogenase, mitochondrial Oxidoreductase C00002657 C00002683 1 / 1
P51580 Thiopurine S-methyltransferase Enzyme C00002682 1 / 1
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00029961 1 / 1
P19793 Retinoic acid receptor RXR-alpha NR2B1 C00002683 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00034390 1 / 0
P00918 Carbonic anhydrase 2 Lyase C00029515 1 / 2
P34969 5-hydroxytryptamine receptor 7 Serotonin receptor C00002683 0 / 0
Q02156 Protein kinase C epsilon type Eta C00034390 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00034390 0 / 1
P15559 NAD(P)H dehydrogenase [quinone] 1 Enzyme C00034390 0 / 0
Q9HAW7 UDP-glucuronosyltransferase 1-7 Enzyme C00002683 0 / 0
P11387 DNA topoisomerase 1 Isomerase C00034390 0 / 0
P11388 DNA topoisomerase 2-alpha Isomerase C00034390 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00000258 2 / 3
P00352 Retinal dehydrogenase 1 Enzyme C00002683 0 / 0
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00034390 0 / 0
Q8TDS4 Hydroxycarboxylic acid receptor 2 Hydroxycarboxylic acid receptor C00029961 0 / 0
P14902 Indoleamine 2,3-dioxygenase 1 Enzyme C00002657 0 / 0
P39748 Flap endonuclease 1 Enzyme C00000258 0 / 0
P08151 Zinc finger protein GLI1 Unclassified protein C00034390 0 / 0
P42858 Huntingtin Unclassified protein C00002682 1 / 1
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00000258 2 / 0
Q8TDU6 G-protein coupled bile acid receptor 1 Steroid-like ligand receptor C00034390 0 / 0
O60656 UDP-glucuronosyltransferase 1-9 Enzyme C00002683 0 / 0
P35218 Carbonic anhydrase 5A, mitochondrial Lyase C00029515 0 / 0
P00915 Carbonic anhydrase 1 Lyase C00029515 0 / 0
P49841 Glycogen synthase kinase-3 beta Gsk C00034390 0 / 0
O00519 Fatty-acid amide hydrolase 1 Enzyme C00002683 0 / 0
Q9Y2D0 Carbonic anhydrase 5B, mitochondrial Lyase C00029515 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00000258 7 / 3
Q04206 Transcription factor p65 Transcription Factor C00034390 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00034390 1 / 1
P06746 DNA polymerase beta Enzyme C00034390 0 / 0
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme C00034390 0 / 0
P51843 Nuclear receptor subfamily 0 group B member 1 Nuclear hormone receptor subfamily 0 group B member 1 C00029476 2 / 2
P78527 DNA-dependent protein kinase catalytic subunit Atypical serine/threonine protein kinase PIKK subfamily C00002683 0 / 0
O60218 Aldo-keto reductase family 1 member B10 Enzyme C00034390 0 / 0
Q13133 Oxysterols receptor LXR-alpha NR1H3 C00034390 0 / 0
P08581 Hepatocyte growth factor receptor TK tyrosine-protein kinase MET subfamily C00029515 2 / 3
P28482 Mitogen-activated protein kinase 1 Erk C00000258 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00034390 0 / 0
P55055 Oxysterols receptor LXR-beta NR1H3 C00034390 0 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002683 2 / 2
Q9Y4X1 UDP-glucuronosyltransferase 2A1 Enzyme C00002683 0 / 0
P49798 Regulator of G-protein signaling 4 Unclassified protein C00034390 2 / 0
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor C00034390 0 / 0
P05771 Protein kinase C beta type Alpha C00034390 0 / 0
P02545 Prelamin-A/C Unclassified protein C00034390 11 / 10
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00034390 1 / 1
Q99700 Ataxin-2 Unclassified protein C00000258 1 / 1
Q9HAW8 UDP-glucuronosyltransferase 1-10 Enzyme C00002683 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00000258 4 / 3
P19224 UDP-glucuronosyltransferase 1-6 Enzyme C00002683 0 / 0
Q16637 Survival motor neuron protein Unclassified protein C00000258 4 / 1
P10275 Androgen receptor NR3C4 C00002683 3 / 4
Q9UBT6 DNA polymerase kappa Enzyme C00034390 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00000258 0 / 0
Q2TB90 Putative hexokinase HKDC1 Enzyme C00000258 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00002683 1 / 1
P04637 Cellular tumor antigen p53 Transcription Factor C00000258 7 / 37
Q8IUX4 DNA dC->dU-editing enzyme APOBEC-3F Enzyme C00034390 0 / 0
O00255 Menin Unclassified protein C00000258 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00000258 1 / 2
Q9UBT2 SUMO-activating enzyme subunit 2 Enzyme C00034390 0 / 0
Q9UBE0 SUMO-activating enzyme subunit 1 Unclassified protein C00034390 0 / 0
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00029961 0 / 0
Q14191 Werner syndrome ATP-dependent helicase Enzyme C00000258 2 / 1

58 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
4846 NOS3, ECNOS, eNOS nitric oxide synthase 3 (endothelial cell) (EC:1.14.13.39) C00002682 C00002689 C00029961
54577 UGT1A7, UDPGT, UDPGT_1-7, UGT-1G, UGT1-07, UGT1.7, UGT1G UDP glucuronosyltransferase 1 family, polypeptide A7 (EC:2.4.1.17) C00002682 C00029961
54576 UGT1A8, UDPGT, UDPGT_1-8, UGT-1H, UGT1-08, UGT1.8, UGT1A8S, UGT1H UDP glucuronosyltransferase 1 family, polypeptide A8 (EC:2.4.1.17) C00002682 C00029961
54659 UGT1A3, UDPGT, UDPGT_1-3, UGT-1C, UGT1-03, UGT1.3, UGT1C UDP glucuronosyltransferase 1 family, polypeptide A3 (EC:2.4.1.17) C00002682 C00029961
54575 UGT1A10, UDPGT, UGT-1J, UGT1-10, UGT1.10, UGT1J UDP glucuronosyltransferase 1 family, polypeptide A10 (EC:2.4.1.17) C00002682 C00029961
2033 EP300, KAT3B, RSTS2, p300 E1A binding protein p300 (EC:2.3.1.48) C00002689
1571 CYP2E1, CPE1, CYP2E, P450-J, P450C2E cytochrome P450, family 2, subfamily E, polypeptide 1 (EC:1.14.13.n7) C00029961
1576 CYP3A4, CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4, HLP, NF-25, P450C3, P450PCN1 cytochrome P450, family 3, subfamily A, polypeptide 4 (EC:1.14.13.67 1.14.13.97 1.14.13.32 1.14.13.157) C00029961
338442 HCAR2, GPR109A, HCA2, HM74a, HM74b, NIACR1, PUMAG, Puma-g hydroxycarboxylic acid receptor 2 C00029961
3284 HSD3B2, HSD3B, HSDB, SDR11E2 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 (EC:1.1.1.145 5.3.3.1) C00029961
1586 CYP17A1, CPT7, CYP17, P450C17, S17AH cytochrome P450, family 17, subfamily A, polypeptide 1 (EC:1.14.99.9 4.1.2.30) C00029961
7299 TYR, ATN, CMM8, OCA1, OCA1A, OCAIA, SHEP3 tyrosinase (EC:1.14.18.1) C00029961
1559 CYP2C9, CPC9, CYP2C, CYP2C10, CYPIIC9, P450IIC9 cytochrome P450, family 2, subfamily C, polypeptide 9 (EC:1.14.13.48 1.14.13.49 1.14.13.80) C00029961
1558 CYP2C8, CPC8, CYPIIC8, MP-12/MP-20 cytochrome P450, family 2, subfamily C, polypeptide 8 (EC:1.14.14.1) C00029961
1557 CYP2C19, CPCJ, CYP2C, P450C2C, P450IIC19 cytochrome P450, family 2, subfamily C, polypeptide 19 (EC:1.14.13.48 1.14.13.49 1.14.13.80) C00029961
1548 CYP2A6, CPA6, CYP2A, CYP2A3, CYPIIA6, P450C2A, P450PB cytochrome P450, family 2, subfamily A, polypeptide 6 (EC:1.14.14.1) C00029961
183 AGT, ANHU, SERPINA8 angiotensinogen (serpin peptidase inhibitor, clade A, member 8) C00002689
1386 ATF2, CRE-BP1, CREB2, HB16, TREB7 activating transcription factor 2 (EC:2.3.1.48) C00002689
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00002689
6356 CCL11, SCYA11 chemokine (C-C motif) ligand 11 C00002689
6362 CCL18, AMAC-1, AMAC1, CKb7, DC-CK1, DCCK1, MIP-4, PARC, SCYA18 chemokine (C-C motif) ligand 18 (pulmonary and activation-regulated) C00002689
6347 CCL2, GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1, SCYA2, SMC-CF chemokine (C-C motif) ligand 2 C00002689
6352 CCL5, D17S136E, RANTES, SCYA5, SIS-delta, SISd, TCP228, eoCP chemokine (C-C motif) ligand 5 C00002689
6354 CCL7, FIC, MARC, MCP-3, MCP3, NC28, SCYA6, SCYA7 chemokine (C-C motif) ligand 7 C00002689
948 CD36, BDPLT10, CHDS7, FAT, GP3B, GP4, GPIV, PASIV, SCARB3 CD36 molecule (thrombospondin receptor) C00002689
1437 CSF2, GMCSF colony stimulating factor 2 (granulocyte-macrophage) C00002689
2919 CXCL1, FSP, GRO1, GROa, MGSA, MGSA-a, NAP-3, SCYB1 chemokine (C-X-C motif) ligand 1 (melanoma growth stimulating activity, alpha) C00002689
3627 CXCL10, C7, IFI10, INP10, IP-10, SCYB10, crg-2, gIP-10, mob-1 chemokine (C-X-C motif) ligand 10 C00002689
1536 CYBB, AMCBX2, CGD, GP91-1, GP91-PHOX, GP91PHOX, NOX2, p91-PHOX cytochrome b-245, beta polypeptide C00002689
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) C00029961
2335 FN1, CIG, ED-B, FINC, FN, FNZ, GFND, GFND2, LETS, MSF fibronectin 1 C00002689
3162 HMOX1, HMOX1D, HO-1, HSP32, bK286B10 heme oxygenase (decycling) 1 (EC:1.14.99.3) C00002689
27429 HTRA2, OMI, PARK13, PRSS25 HtrA serine peptidase 2 (EC:3.4.21.108) C00002689
3383 ICAM1, BB2, CD54, P3.58 intercellular adhesion molecule 1 C00002689
3456 IFNB1, IFB, IFF, IFNB interferon, beta 1, fibroblast C00002689
3553 IL1B, IL-1, IL1-BETA, IL1F2 interleukin 1, beta C00002689
3569 IL6, BSF2, HGF, HSF, IFNB2, IL-6 interleukin 6 (interferon, beta 2) C00002689
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00002689
3684 ITGAM, CD11B, CR3A, MAC-1, MAC1A, MO1A, SLEB6 integrin, alpha M (complement component 3 receptor 3 subunit) C00002689
3717 JAK2, JTK10, THCYT3 Janus kinase 2 (EC:2.7.10.2) C00002689
3725 JUN, AP-1, AP1, c-Jun jun proto-oncogene C00002689
5594 MAPK1, ERK, ERK2, ERT1, MAPK2, P42MAPK, PRKM1, PRKM2, p38, p40, p41, p41mapk mitogen-activated protein kinase 1 (EC:2.7.11.24) C00002689
5595 MAPK3, ERK-1, ERK1, ERT2, HS44KDAP, HUMKER1A, P44ERK1, P44MAPK, PRKM3, p44-ERK1, p44-MAPK mitogen-activated protein kinase 3 (EC:2.7.11.24) C00002689
5599 MAPK8, JNK, JNK-46, JNK1, JNK1A2, JNK21B1/2, PRKM8, SAPK1, SAPK1c mitogen-activated protein kinase 8 (EC:2.7.11.24) C00002689
5601 MAPK9, JNK-55, JNK2, JNK2A, JNK2ALPHA, JNK2B, JNK2BETA, PRKM9, SAPK, SAPK1a, p54a, p54aSAPK mitogen-activated protein kinase 9 (EC:2.7.11.24) C00002689
4282 MIF, GIF, GLIF, MMIF macrophage migration inhibitory factor (glycosylation-inhibiting factor) (EC:5.3.3.12 5.3.2.1) C00002689
4322 MMP13, CLG3, MANDP1 matrix metallopeptidase 13 (collagenase 3) (EC:3.4.24.-) C00002689
4481 MSR1, CD204, SCARA1, SR-A, SRA, phSR1, phSR2 macrophage scavenger receptor 1 C00002689
653361 NCF1, NCF1A, NOXO2, SH3PXD1A, p47phox neutrophil cytosolic factor 1 C00002689
4792 NFKBIA, IKBA, MAD-3, NFKBI nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha C00002689
4973 OLR1, CLEC8A, LOX1, LOXIN, SCARE1, SLOX1 oxidized low density lipoprotein (lectin-like) receptor 1 C00002689
5743 PTGS2, COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2, hCox-2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase) (EC:1.14.99.1) C00002689
5970 RELA, NFKB3, p65 v-rel avian reticuloendotheliosis viral oncogene homolog A C00002689
5054 SERPINE1, PAI, PAI-1, PAI1, PLANH1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1 C00002689
6772 STAT1, CANDF7, ISGF-3, STAT91 signal transducer and activator of transcription 1, 91kDa C00002689
7082 TJP1, ZO-1 tight junction protein 1 C00002689
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00002689
7412 VCAM1, CD106, INCAM-100 vascular cell adhesion molecule 1 C00002689

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (65)

OMIM preferred title UniProt
#300018 46,xy sex reversal 2; srxy2 P51843
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#300200 Adrenal hypoplasia, congenital; ahc P51843
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#114500 Colorectal cancer; crc P84022
Q14191
#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
#615363 Estrogen resistance; estrr P03372
#600274 Frontotemporal dementia; ftd P10636
#613163 Gaba-transaminase deficiency P80404
#137800 Glioma susceptibility 1; glm1 O75874
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610140 Heart-hand syndrome, slovenian type P02545
#114550 Hepatocellular carcinoma P08581
#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
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#211980 Lung cancer P04637
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#174800 Mccune-albright syndrome; mas P63092
#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
#166350 Osseous heteroplasia, progressive; poh P63092
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#260500 Papilloma of choroid plexus; cpp P04637
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#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
#605074 Renal cell carcinoma, papillary, 1; rccp1 P08581
#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
#271980 Succinic semialdehyde dehydrogenase deficiency; ssadhd P51649
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#610460 Thiopurine s-methyltransferase deficiency P51580
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#277700 Werner syndrome; wrn Q14191
#278300 Xanthinuria, type i P47989
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (83)

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)
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (related)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (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)
H00004 Chronic myeloid leukemia (CML) P04637 (related)
H00005 Chronic lymphocytic leukemia (CLL) P04637 (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)
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)
P08581 (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)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
H00032 Thyroid cancer P04637 (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)
H00042 Glioma P04637 (related)
P04637 (marker)
H00044 Cancer of the anal canal P04637 (related)
H00046 Cholangiocarcinoma P04637 (related)
P08581 (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)
P08581 (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)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (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)
H00059 Huntington's disease (HD) P42858 (related)
H00192 Xanthinuria P47989 (related)
H00964 Thiopurine S-methyltransferase deficiency (TPMT deficiency) P51580 (related)
H00835 Succinic semialdehyde dehydrogenase (SSADH) deficiency P51649 (related)
H00552 Glycerol kinase deficiency (GKD) P51843 (related)
H00607 46,XY disorders of sex development (Disorders of gonadal development) P51843 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H01257 GABA-transaminase deficiency P80404 (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)
H00296 Defects in RecQ helicases Q14191 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

12 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D003384 Coxsackievirus Infections C00029961
D008545 Melanoma C00029961
D000419 Albuminuria C00002689
D001919 Bradycardia C00002689
D020520 Brain Infarction C00002689
D002310 Cardiomyopathy, Alcoholic C00002689
D003928 Diabetic Nephropathies C00002689
D006331 Heart Diseases C00002689
D006973 Hypertension C00002689
D007022 Hypotension C00002689
D009410 Nerve Degeneration C00002689
D011014 Pneumonia C00002689