Species

KNApSAcK Entry

Organism name Erythrina variegata
Genus Erythrina
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Erythrina variegata
Linked NCBI taxonomy ID 3845
Linked level species

Family

Family in NCBI taxonomy Fabaceae
ID 3803

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (47)

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
C00009516 External link 512 6,8-Diprenylgenistein
/ 8-(gamma,gamma-Dimethylallyl)wighteone
/ 5,7,4'-Trihydroxy-6,8-diprenylisoflavone
CHEMBL494252
12 / 14 / 11 No. 14 No. 15
C00019741 External link 512 Eryvarin E
/ 3-Hydroxy-9-methoxy-2,10-diprenylpterocarpan
No. 14 No. 15
C00018965 External link 512 Erysubin F
CHEMBL2159045
1 / 0 / 0 No. 14 No. 15
C00010027 External link 512 Erycristagallin
/ 3,9-Dihydroxy-2,10-diprenylpterocarpene
CHEMBL462699
1 / 0 / 0 No. 14 No. 15
C00002586 External link 512 Wighteone
/ Erythrinin B
/ 5,7,4'-Trihydroxy-6-prenylisoflavone
CHEMBL393222
2 / 1 / 1 No. 15 No. 15
C00018966 External link 512 Eryvarin D
CHEMBL1097045
No. 15 No. 15
C00002555 External link 512 Osajin
CHEMBL238188
36 / 50 / 70 No. 18 No. 15
C00009948 External link 512 Euchrenone b9
No. 18 No. 15
C00009521 External link 512 Auriculatin
No. 18 No. 15
C00009514 External link 512 Scandenone
/ Warangalone
CHEMBL458134
C105205
No. 18 No. 15
C00018981 External link 512 (-)-Bidwillon A
/ 7,2',4'-Trihydroxy-6,8-diprenylisoflavanone
No. 19 No. 14
C00009492 External link 512 Alpinumisoflavone
CHEMBL238628
C000154
3 / 1 / 1 1 / 0 No. 24 No. 15
C00019381 External link 512 Bidwillon C
/ 4'-Hydroxy-6'',6''-dimethylpyrano[2'',3'':7,8]isoflavone
CHEMBL1214836
1 / 1 / 1 No. 24 No. 15
C00009431 External link 512 Erythrinin A
No. 24 No. 15
C00008197 External link 512 Isobavachin
CHEMBL491534
C468753
2 / 0 No. 28 No. 14
C00018985 External link 512 Bidwillon B
No. 39
C00018984 External link 512 Orientanol F
/ 2',4'-Dihydroxy-6-prenyl-6'',6''-dimethylpyrano[2'',3'':7,8]isoflavanone
No. 39
C00019725 External link 512 Eryvarin B
/ 7,4'-Dihydroxy-5''-(1-hydroxy-1-methylethyl)-8'-prenyl-6'',6''-dimethyl-4'',5''-dihydropyrano[2'',3'':5,6]isoflavone
No. 47 No. 15
C00019069 External link 512 Erysubin C
/ (6aR,11aR)-2-Carboxyaldehyde-9-hydroxy-3-methoxypterocarpan
No. 66 No. 15
C00019740 External link 512 Eryvarin C
/ (3R)-2',4'-Dihydroxy-6'',6''-dimethylpyrano[2'',3'':7,6]isoflavan
No. 135 No. 15
C00002559 External link 512 Phaseolin
/ (-)-Phaseollin
CHEMBL448350
No. 135 No. 15
C00009501 External link 512 Erythrinin C
No. 139
C00019377 External link 512 Erythrivarone A
/ 5,4'-Dihydroxy-6'',6''-dimethyl-4'',5''-dihydropyrano[2'',3'':7,6]isoflavone
No. 139
C00019738 External link 512 Eryvarin K
/ 3,9-Dihydroxy-8-methoxy-4-prenylpterocarpan
CHEMBL1079408
1 / 0 / 0 No. 188 No. 15
C00018899 External link 512 Orientanol B
/ 3-O-Methylcalopocarpin
CHEMBL465985
No. 188 No. 15
C00002558 External link 512 Phaseollidin
CHEMBL508534
C085158
1 / 0 / 0 No. 188 No. 15
C00019739 External link 512 Eryvarin L
/ 6,4'-Dihydroxy-2',5'-dimethoxy-2-arybenzofuran
No. 210 No. 15
C00002893 External link 512 Oxyresveratrol
/ 2,3,4,5'-Tetrahydroxystilbene
CHEMBL43065
20 / 32 / 49 No. 295 No. 13
C00002515 External link 512 Cristacarpin
/ Erythrabyssin I
CHEMBL454849
C085157
2 / 1 / 1 No. 325 No. 15
C00019724 External link 512 Eryvarin A
/ (6aS,11aS,5'S)-3,6a,5'-Trihydroxy-6',6'-dimethyl-4',5'-dihydropyrano[2',3':9,10]pterocarpan
CHEMBL269337
No. 325 No. 15
C00009664 External link 512 Folitenol
CHEMBL551155
1 / 0 / 0 No. 352 No. 15
C00018967 External link 512 Orientanol C
No. 352 No. 15
C00018947 External link 512 Bidwillol A
No. 400
C00019735 External link 512 Eryvarin H
/ 7,4'-Dihydroxy-2',5'-dimethoxyisoflav-3-ene
No. 400
C00018969 External link 512 Sigmoidin K
/ 3,9-Dihydroxy-2,10-diprenylcoumestan
CHEMBL1095262
C090620
No. 436 No. 17
C00027356 External link 512 Erythrartine
/ (+)-Erythrartine
/ 11-Hydroxyerysotrine
CHEMBL217996
No. 446 No. 4
C00010024 External link 512 2-Prenyl-6a-hydroxyphaseollidin
/ 3,6a,9-Trihydroxy-2,10-diprenylpterocarpan
No. 460
C00009669 External link 512 Erythrabyssin II
/ 3,9-Dihydroxy-2,10-diprenylpterocarpan
CHEMBL455372
1 / 0 / 0 No. 460
C00018930 External link 512 Erystagallin A
CHEMBL1088462
1 / 0 / 0 No. 460
C00019737 External link 512 Eryvarin J
/ 3,9-Dihydroxy-2,4-diprenylpterocarpan
No. 460
C00019378 External link 512 Erythrivarone B
No. 724
C00000615 External link 512 Caffeic acid
CHEMBL145
CHEMBL1320034
68 / 64 / 63 No. 904 No. 6
C00019068 External link 512 Laburnetin
/ 5,7,4',2''-Tetrahydroxy-6-[3''-methyl-3''-butenyl]isoflavone
No. 984
C00020453 External link 512 Eryvariestyrene
No. 1271 No. 13
C00019736 External link 512 Eryvarin I
/ 3-Hydroxy-2'-methoxy-6'',6''-dimethylpyrano[2'',3'':4',3']isoflav-3-ene
No. 2189
C00002074 External link 512 Stachydrine
CHEMBL394450
CHEMBL1456892
CHEMBL1986864
10 / 8 / 12 No. 2627 No. 1
C00001854 External link 512 beta-Erythroidine
C004873
No. 4287 No. 4

Human Protein / Gene in interactions

100 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00000615 C00002558 C00009492 C00009664 C00009669 C00018930 C00018965 C00019738 0 / 0
P03372 Estrogen receptor NR3A1 C00000615 C00002515 C00002586 C00009492 C00019381 1 / 1
O75164 Lysine-specific demethylase 4A Enzyme C00000615 C00002555 C00002893 C00009516 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000615 C00002074 C00002555 0 / 1
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00000615 C00002074 C00002555 1 / 2
Q92731 Estrogen receptor beta NR3A2 C00002515 C00002586 C00009492 0 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00000615 C00002074 C00002893 0 / 0
O00255 Menin Unclassified protein C00000615 C00002074 C00002555 2 / 5
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00002555 C00002893 C00009516 1 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00000615 C00002555 C00009516 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00000615 C00002555 C00009516 4 / 3
P14780 Matrix metalloproteinase-9 M10A C00000615 C00002893 2 / 2
P06746 DNA polymerase beta Enzyme C00000615 C00002555 0 / 0
P04062 Glucosylceramidase Enzyme C00002555 C00009516 6 / 4
P10253 Lysosomal alpha-glucosidase Hydrolase C00000615 C00002555 1 / 1
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00002555 C00009516 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00000615 C00002555 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00000615 C00002555 0 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00000615 C00002893 0 / 3
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00002555 C00009516 2 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00000615 C00002555 0 / 0
Q99700 Ataxin-2 Unclassified protein C00002555 C00009516 1 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000615 C00002074 1 / 1
P02545 Prelamin-A/C Unclassified protein C00000615 C00002555 11 / 10
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00000615 C00002555 0 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00000615 C00002074 3 / 2
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00002893 C00009516 0 / 0
P08253 72 kDa type IV collagenase M10A C00000615 C00002893 1 / 3
P01215 Glycoprotein hormones alpha chain Unclassified protein C00002555 C00009516 0 / 3
P04637 Cellular tumor antigen p53 Transcription Factor C00002555 C00002893 7 / 37
P14679 Tyrosinase Oxidoreductase C00000615 C00002893 4 / 2
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000615 C00002074 0 / 1
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00002074 C00002555 0 / 0
P03956 Interstitial collagenase M10A C00000615 C00002893 0 / 1
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00000615 C00002893 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00002555 C00009516 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000615 C00002074 1 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00000615 C00002555 0 / 0
P17405 Sphingomyelin phosphodiesterase Enzyme C00002555 C00002893 2 / 2
P38398 Breast cancer type 1 susceptibility protein Enzyme C00002555 C00002893 4 / 2
O75496 Geminin Unclassified protein C00002555 C00009516 0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00002555 C00002893 1 / 1
Q8TDS4 Hydroxycarboxylic acid receptor 2 Hydroxycarboxylic acid receptor C00000615 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00002074 0 / 0
P42858 Huntingtin Unclassified protein C00002555 1 / 1
P42330 Aldo-keto reductase family 1 member C3 Enzyme C00000615 0 / 0
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00000615 0 / 0
O43570 Carbonic anhydrase 12 Lyase C00000615 1 / 2
Q9ULX7 Carbonic anhydrase 14 Lyase C00000615 0 / 0
P15121 Aldose reductase Enzyme C00000615 0 / 0
P00915 Carbonic anhydrase 1 Lyase C00000615 0 / 0
P23280 Carbonic anhydrase 6 Lyase C00000615 0 / 0
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00000615 1 / 8
Q9Y253 DNA polymerase eta Enzyme C00002555 1 / 1
P11021 78 kDa glucose-regulated protein Unclassified protein C00002555 0 / 0
Q9GZT9 Egl nine homolog 1 Enzyme C00000615 1 / 1
P51452 Dual specificity protein phosphatase 3 Ser_Thr_Tyr C00000615 0 / 0
Q16678 Cytochrome P450 1B1 Cytochrome P450 1B1 C00002893 4 / 4
P06280 Alpha-galactosidase A Enzyme C00000615 1 / 1
P45452 Collagenase 3 M10A C00002893 1 / 1
P35236 Tyrosine-protein phosphatase non-receptor type 7 Tyr C00000615 0 / 0
P04798 Cytochrome P450 1A1 Cytochrome P450 1A1 C00002893 0 / 0
P00918 Carbonic anhydrase 2 Lyase C00000615 1 / 2
Q16790 Carbonic anhydrase 9 Lyase C00000615 0 / 1
P10828 Thyroid hormone receptor beta NR1A2 C00000615 3 / 1
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00000615 3 / 3
Q04828 Aldo-keto reductase family 1 member C1 Enzyme C00000615 0 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00000615 2 / 2
Q01453 Peripheral myelin protein 22 Unclassified protein C00000615 5 / 2
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00000615 1 / 1
P37840 Alpha-synuclein Unclassified protein C00002893 4 / 2
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor C00000615 0 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme C00002555 0 / 0
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00002555 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00002555 0 / 0
P39900 Macrophage metalloelastase M10A C00002893 0 / 0
P52895 Aldo-keto reductase family 1 member C2 Enzyme C00000615 1 / 0
Q06124 Tyrosine-protein phosphatase non-receptor type 11 Tyr C00000615 4 / 2
P43166 Carbonic anhydrase 7 Lyase C00000615 0 / 0
P35218 Carbonic anhydrase 5A, mitochondrial Lyase C00000615 0 / 0
Q9Y2D0 Carbonic anhydrase 5B, mitochondrial Lyase C00000615 0 / 0
P07451 Carbonic anhydrase 3 Lyase C00000615 0 / 0
P08254 Stromelysin-1 M10A C00002893 1 / 0
P04054 Phospholipase A2 Enzyme C00010027 0 / 0
P22748 Carbonic anhydrase 4 Lyase C00000615 1 / 1
Q12794 Hyaluronidase-1 Enzyme C00000615 1 / 2
Q13093 Platelet-activating factor acetylhydrolase Enzyme C00000615 3 / 0
P24298 Alanine aminotransferase 1 Enzyme C00000615 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00000615 0 / 0
O00167 Eyes absent homolog 2 Enzyme C00002555 0 / 0
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00000615 2 / 2
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00000615 1 / 1
P09917 Arachidonate 5-lipoxygenase Oxidoreductase C00000615 0 / 0
O60218 Aldo-keto reductase family 1 member B10 Enzyme C00000615 0 / 0
Q16637 Survival motor neuron protein Unclassified protein C00002555 4 / 1
P07900 Heat shock protein HSP 90-alpha Other cytosolic protein C00000615 0 / 0
P08238 Heat shock protein HSP 90-beta Other cytosolic protein C00000615 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00000615 0 / 0
P17516 Aldo-keto reductase family 1 member C4 Enzyme C00000615 1 / 0
Q6W5P4 Neuropeptide S receptor Neuropeptide receptor C00002555 1 / 0

3 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
3091 HIF1A, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1, PASD8, bHLHe78 hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor) C00009492
5241 PGR, NR3C3, PR progesterone receptor C00008197
7031 TFF1, BCEI, D21S21, HP1.A, HPS2, pNR-2, pS2 trefoil factor 1 C00008197

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (103)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#614279 46,xy sex reversal 8; srxy8 P17516
P52895
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#103470 Albinism, ocular, with sensorineural deafness P14679
#203100 Albinism, oculocutaneous, type ia; oca1a P14679
#606952 Albinism, oculocutaneous, type ib; oca1b P14679
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#600807 Asthma, susceptibility to Q13093
#608584 Asthma-related traits, susceptibility to, 2 Q6W5P4
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#114480 Breast cancer P38398
#604370 Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 P38398
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#118300 Charcot-marie-tooth disease and deafness Q01453
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#118220 Charcot-marie-tooth disease, demyelinating, type 1a; cmt1a Q01453
#114500 Colorectal cancer; crc P84022
#614466 Coronary heart disease, susceptibility to, 6; chds6 P08254
#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
#609820 Erythrocytosis, familial, 3; ecyt3 Q9GZT9
#133239 Esophageal cancer P04637
#615363 Estrogen resistance; estrr P03372
#301500 Fabry disease P06280
#600274 Frontotemporal dementia; ftd P10636
#608013 Gaucher disease, perinatal lethal P04062
#230800 Gaucher disease, type i P04062
#230900 Gaucher disease, type ii P04062
#231000 Gaucher disease, type iii P04062
#231005 Gaucher disease, type iiic P04062
#137750 Glaucoma 1, open angle, a; glc1a Q16678
#231300 Glaucoma 3, primary congenital, a; glc3a Q16678
#137760 Glaucoma, primary open angle; poag Q16678
#137800 Glioma susceptibility 1; glm1 O75874
#232300 Glycogen storage disease ii P10253
#139393 Guillain-barre syndrome, familial; gbs Q01453
#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
#143860 Hyperchlorhidrosis, isolated O43570
#145000 Hyperparathyroidism 1; hrpt1 O00255
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#145900 Hypertrophic neuropathy of dejerine-sottas Q01453
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#147050 Ige responsiveness, atopic; iger Q13093
#603932 Intervertebral disc disease; idd P14780
#607785 Juvenile myelomonocytic leukemia; jmml Q06124
#151100 Leopard syndrome 1 Q06124
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#613688 Long qt syndrome 2; lqt2 Q12809
#211980 Lung cancer P00533
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
#156250 Metachondromatosis; metcds Q06124
#613073 Metaphyseal anadysplasia 2; mandp2 P14780
#601492 Mucopolysaccharidosis, type ix; mps9 Q12794
#259600 Multicentric osteolysis, nodulosis, and arthropathy; mona P08253
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#162500 Neuropathy, hereditary, with liability to pressure palsies; hnpp Q01453
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#163950 Noonan syndrome 1; ns1 Q06124
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#167000 Ovarian cancer P38398
#614320 Pancreatic cancer, susceptibility to, 4; pnca4 P38398
#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 P04062
P37840
#260540 Parkinson-dementia syndrome P10636
#604229 Peters anomaly Q16678
#172700 Pick disease of brain P10636
#614278 Platelet-activating factor acetylhydrolase deficiency; pafad Q13093
#275210 Restrictive dermopathy, lethal P02545
#600852 Retinitis pigmentosa 17; rp17 P22748
#609620 Short qt syndrome 1; sqt1 Q12809
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679
#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
#602111 Spondyloepimetaphyseal dysplasia, missouri type P45452
#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
#278300 Xanthinuria, type i P47989
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (102)

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)
H01302 Hyperchlorhidrosis isolated (HCHLH) O43570 (related)
H00021 Renal cell carcinoma O43570 (marker)
P04637 (marker)
Q16790 (marker)
H00016 Oral cancer P00533 (related)
P00533 (marker)
P04637 (related)
P04637 (marker)
H00017 Esophageal cancer P00533 (related)
P04637 (related)
P04637 (marker)
P35354 (related)
H00018 Gastric cancer P00533 (related)
P04637 (related)
H00022 Bladder cancer P00533 (related)
P04637 (related)
H00028 Choriocarcinoma P00533 (related)
P03956 (related)
P04637 (related)
P08253 (related)
H00030 Cervical cancer P00533 (related)
H00042 Glioma P00533 (related)
P00533 (marker)
P04637 (related)
P04637 (marker)
H00055 Laryngeal cancer P00533 (related)
P00533 (marker)
P04637 (related)
P04637 (marker)
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (related)
H00081 Hashimoto's thyroiditis P01215 (marker)
H00082 Graves' disease P01215 (marker)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P01215 (marker)
P16473 (related)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
Q01453 (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)
Q92731 (marker)
H00066 Lewy body dementia (LBD) P04062 (related)
P37840 (related)
H00126 Gaucher disease P04062 (related)
H00426 Defects in the degradation of ganglioside P04062 (related)
H00810 Progressive myoclonic epilepsy (PME) P04062 (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)
H00019 Pancreatic cancer P04637 (related)
P04637 (marker)
H00020 Colorectal cancer P04637 (related)
P04637 (marker)
H00025 Penile cancer P04637 (related)
P04637 (marker)
P08253 (related)
P14780 (related)
P35354 (related)
H00027 Ovarian cancer P04637 (related)
P38398 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
P38398 (related)
H00032 Thyroid cancer P04637 (related)
H00036 Osteosarcoma P04637 (related)
P08684 (marker)
H00038 Malignant melanoma P04637 (related)
P14679 (marker)
H00039 Basal cell carcinoma P04637 (related)
H00040 Squamous cell carcinoma P04637 (related)
H00041 Kaposi's sarcoma P04637 (related)
H00044 Cancer of the anal canal P04637 (related)
H00046 Cholangiocarcinoma P04637 (related)
P35354 (related)
H00047 Gallbladder cancer P04637 (related)
H00048 Hepatocellular carcinoma P04637 (related)
H00881 Li-Fraumeni syndrome P04637 (related)
H01007 Choroid plexus papilloma P04637 (related)
H00125 Fabry disease P06280 (related)
H00472 Torg-Winchester syndrome P08253 (related)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H01205 Coumarin resistance P11712 (related)
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00479 Metaphyseal dysplasias P14780 (related)
P45452 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)
H00527 Retinitis pigmentosa (RP) P22748 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00057 Parkinson's disease (PD) P37840 (related)
H00059 Huntington's disease (HD) P42858 (related)
H00192 Xanthinuria P47989 (related)
H01296 Hereditary neuropathy with liability to pressure palsies (HNPP) Q01453 (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)
H00523 Noonan syndrome and related disorders Q06124 (related)
H01018 Metachondromatosis Q06124 (related)
H00133 Mucopolysaccharidosis type IX (MPS9) Q12794 (related)
H00421 Mucopolysaccharidosis (MPS) Q12794 (related)
H00720 Long QT syndrome Q12809 (related)
H00725 Short QT syndrome Q12809 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)
H00612 Primary open angle glaucoma Q16678 (related)
H01075 Peters anomaly Q16678 (related)
H01159 Anterior segment dysgenesis (ASD) Q16678 (related)
H01203 Primary congenital glaucoma (PCG) Q16678 (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)
H00236 Congenital polycythemia Q9GZT9 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)