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Browse result for Cardiovascular phenotype

※ introduction

    Cardiovascular disease (CVD) is any disease involving the heart or blood vessels. CVDs constitute a class of diseases that includes: coronary artery diseases (e.g. angina, heart attack), heart failure, hypertensive heart disease, rheumatic heart disease, cardiomyopathy, arrhythmia, congenital heart disease, valvular heart disease, carditis, aortic aneurysms, peripheral artery disease, thromboembolic disease, and venous thrombosis. The underlying mechanisms vary depending on the disease. It is estimated that dietary risk factors are associated with 53% of CVD deaths. Coronary artery disease, stroke, and peripheral artery disease involve atherosclerosis. This may be caused by high blood pressure, smoking, diabetes mellitus, lack of exercise, obesity, high blood cholesterol, poor diet, excessive alcohol consumption, and poor sleep, among other things. High blood pressure is estimated to account for approximately 13% of CVD deaths, while tobacco accounts for 9%, diabetes 6%, lack of exercise 6%, and obesity 5%. Rheumatic heart disease may follow untreated strep throat. It is estimated that up to 90% of CVD may be preventable. Prevention of CVD involves improving risk factors through: healthy eating, exercise, avoidance of tobacco smoke and limiting alcohol intake. Treating risk factors, such as high blood pressure, blood lipids and diabetes is also beneficial. Treating people who have strep throat with antibiotics can decrease the risk of rheumatic heart disease. The use of aspirin in people who are otherwise healthy is of unclear benefit. Cardiovascular diseases are the leading cause of death worldwide except Africa. Together CVD resulted in 17.9 million deaths (32.1%) in 2015, up from 12.3 million (25.8%) in 1990. Deaths, at a given age, from CVD are more common and have been increasing in much of the developing world, while rates have declined in most of the developed world since the 1970s. Coronary artery disease and stroke account for 80% of CVD deaths in males and 75% of CVD deaths in females. Most cardiovascular disease affects older adults. In the United States 11% of people between 20 and 40 have CVD, while 37% between 40 and 60, 71% of people between 60 and 80, and 85% of people over 80 have CVD. The average age of death from coronary artery disease in the developed world is around 80, while it is around 68 in the developing world. CVD is typically diagnosed seven to ten years earlier in men than in women.:?48?

Reference
Wiki: Cardiovascular phenotype



PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD00154O956772070
EYA4
Eyes absent homolog 4
Homo sapiens
PTMD00500P025454000
LMNA
Prelamin-A/C [Cleaved into: Lamin-A/C ]
Homo sapiens
PTMD00305P040495894
RAF1
RAF proto-oncogene serine/threonine-protein kinase
Homo sapiens
PTMD00518P085904634
MYL3
Myosin light chain 3
Homo sapiens
PTMD00243P134733920
LAMP2
Lysosome-associated membrane glycoprotein 2
Homo sapiens
PTMD00540P149233728
JUP
Junction plakoglobin
Homo sapiens
PTMD00896P182067414
VCL
Vinculin
Homo sapiens
PTMD00556P213332316
FLNA
Filamin-A
Homo sapiens
PTMD00588P368977046
TGFBR1
TGF-beta receptor type-1
Homo sapiens
PTMD00254P371737048
TGFBR2
TGF-beta receptor type-2
Homo sapiens
PTMD00179P465314851
NOTCH1
Neurogenic locus notch homolog protein 1 [Cleaved into: Notch 1 extracellular truncation ; Notch 1 intracellular domain ]
Homo sapiens
PTMD00252P840224088
SMAD3
Mothers against decapentaplegic homolog 3
Homo sapiens
PTMD00665Q0ZGT291624
NEXN
Nexilin
Homo sapiens
PTMD00147Q134854089
SMAD4
Mothers against decapentaplegic homolog 4
Homo sapiens
PTMD00700Q157464638
MYLK
Myosin light chain kinase, smooth muscle [Cleaved into: Myosin light chain kinase, smooth muscle, deglutamylated form]
Homo sapiens
PTMD00924Q165952395
FXN
Frataxin, mitochondrial [Cleaved into: Frataxin intermediate form ; Frataxin ; Frataxin ; Frataxin mature form ) ; Extramitochondrial frataxin]
Homo sapiens
PTMD00051Q166356901
TAFAZZIN
Tafazzin
Homo sapiens
PTMD02221E7EWK110587
TXNRD2
Thioredoxin reductase 2
Homo sapiens
PTMD01461P025111410
CRYAB
Alpha-crystallin B chain -crystallin)
Homo sapiens
PTMD01064P094937168
TPM1
Tropomyosin alpha-1 chain
Homo sapiens
PTMD01525P159241832
DSP
Desmoplakin
Homo sapiens
PTMD01606P355552200
FBN1
Fibrillin-1 [Cleaved into: Asprosin]
Homo sapiens
PTMD01694P6803270
ACTC1
Actin, alpha cardiac muscle 1 [Cleaved into: Actin, alpha cardiac muscle 1, intermediate form]
Homo sapiens
PTMD01733Q128093757
KCNH2
Potassium voltage-gated channel subfamily H member 2
Homo sapiens
PTMD01751Q145246331
SCN5A
Sodium channel protein type 5 subunit alpha
Homo sapiens
PTMD01131Q148964607
MYBPC3
Myosin-binding protein C, cardiac-type
Homo sapiens
PTMD01845Q8WZ427273
TTN
Titin
Homo sapiens
PTMD01162Q927366262
RYR2
Ryanodine receptor 2
Homo sapiens
PTMD01878Q9BR3957158
JPH2
Junctophilin-2 [Cleaved into: Junctophilin-2 N-terminal fragment ]
Homo sapiens
PTMD02978O609396327
SCN2B
Sodium channel subunit beta-2
Homo sapiens
PTMD03005O7511211155
LDB3
LIM domain-binding protein 3
Homo sapiens
PTMD03465O9552881031
SLC2A10
Solute carrier family 2, facilitated glucose transporter member 10
Homo sapiens
PTMD03789P062802717
GLA
Alpha-galactosidase A
Homo sapiens
PTMD04056P109164633
MYL2
Myosin regulatory light chain 2, ventricular/cardiac muscle isoform
Homo sapiens
PTMD04088P115321756
DMD
Dystrophin
Homo sapiens
PTMD04124P127556497
SKI
Ski oncogene
Homo sapiens
PTMD04130P128834625
MYH7
Myosin-7
Homo sapiens
PTMD04145P135334624
MYH6
Myosin-6
Homo sapiens
PTMD04456P209081289
COL5A1
Collagen alpha-1 chain
Homo sapiens
PTMD04933P3552010272
CBS
Cystathionine beta-synthase
Homo sapiens
PTMD04938P355562201
FBN2
Fibrillin-2 [Cleaved into: Placensin]
Homo sapiens
PTMD04944P3560988
ACTN2
Alpha-actinin-2
Homo sapiens
PTMD04957P357494629
MYH11
Myosin-11
Homo sapiens
PTMD05083P421667112
TMPO
Lamina-associated polypeptide 2, isoform alpha [Cleaved into: Thymopoietin ; Thymopentin ]
Homo sapiens
PTMD05377P504022010
EMD
Emerin
Homo sapiens
PTMD05384P504618048
CSRP3
Cysteine and glycine-rich protein 3
Homo sapiens
PTMD05456P517873784
KCNQ1
Potassium voltage-gated channel subfamily KQT member 1
Homo sapiens
PTMD05493P521798736
MYOM1
Myomesin-1
Homo sapiens
PTMD05876P6273659
ACTA2
Actin, aortic smooth muscle [Cleaved into: Actin, aortic smooth muscle, intermediate form]
Homo sapiens
PTMD06110Q01484287
ANK2
Ankyrin-2
Homo sapiens
PTMD06160Q024871824
DSC2
Desmocollin-2
Homo sapiens
PTMD06169Q028095351
PLOD1
Procollagen-lysine,2-oxoglutarate 5-dioxygenase 1
Homo sapiens
PTMD06443Q1306110345
TRDN
Triadin
Homo sapiens
PTMD06532Q134183611
ILK
Integrin-linked protein kinase
Homo sapiens
PTMD06654Q139765592
PRKG1
cGMP-dependent protein kinase 1
Homo sapiens
PTMD06676Q141261829
DSG2
Desmoglein-2
Homo sapiens
PTMD06937Q1532727063
ANKRD1
Ankyrin repeat domain-containing protein 1
Homo sapiens
PTMD07043Q158423764
KCNJ8
ATP-sensitive inward rectifier potassium channel 8 channel Kir6.1)
Homo sapiens
PTMD07079Q163633910
LAMA4
Laminin subunit alpha-4
Homo sapiens
PTMD07741Q5T48128299
RBM20
RNA-binding protein 20
Homo sapiens
PTMD08964Q86TC984665
MYPN
Myopalladin
Homo sapiens
PTMD09624Q8N33523171
GPD1L
Glycerol-3-phosphate dehydrogenase 1-like protein
Homo sapiens
PTMD10363Q8TD4354795
TRPM4
Transient receptor potential cation channel subfamily M member 4
Homo sapiens
PTMD10882Q930749968
MED12
Mediator of RNA polymerase II transcription subunit 12
Homo sapiens
PTMD11843Q995936910
TBX5
T-box transcription factor TBX5
Homo sapiens
PTMD11923Q999595318
PKP2
Plakophilin-2
Homo sapiens
PTMD12114Q9BTV479188
TMEM43
Transmembrane protein 43
Homo sapiens
PTMD14271Q9UK173752
KCND3
Potassium voltage-gated channel subfamily D member 3
Homo sapiens
PTMD14458Q9UMR357057
TBX20
T-box transcription factor TBX20
Homo sapiens
PTMD14801Q9Y3Q410021
HCN4
Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 4
Homo sapiens