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Browse result for Long QT syndrome

※ introduction

    An autosomal genetic disease that is characterized by delayed repolarization of the heart following a heartbeat increases the risk of episodes of torsade de pointes (TDP, a form of irregular heartbeat that originates from the ventricles).

Reference
DiseaseOntology: Long QT syndrome


PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD00970P527323832
KIF11
Kinesin-like protein KIF11
Homo sapiens
PTMD00743Q8N6T751548
SIRT6
NAD-dependent protein deacylase sirtuin-6
Homo sapiens
PTMD01065P0DP2380180
CALM1
Calmodulin-1
Homo sapiens
PTMD01097P434056850
SYK
Tyrosine-protein kinase SYK
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
PTMD01162Q927366262
RYR2
Ryanodine receptor 2
Homo sapiens
PTMD02251O00192421
ARVCF
Splicing regulator ARVCF
Homo sapiens
PTMD02985O7503723046
KIF21B
Kinesin-like protein KIF21B
Homo sapiens
PTMD03346O9507151366
UBR5
E3 ubiquitin-protein ligase UBR5
Homo sapiens
PTMD04078P113887153
TOP2A
DNA topoisomerase 2-alpha
Homo sapiens
PTMD04234P153823753
KCNE1
Potassium voltage-gated channel subfamily E member 1
Homo sapiens
PTMD04370P188276382
SDC1
Syndecan-1
Homo sapiens
PTMD05161P460134288
MKI67
Proliferation marker protein Ki-67
Homo sapiens
PTMD05248P485443762
KCNJ5
G protein-activated inward rectifier potassium channel 4 channel Kir3.4)
Homo sapiens
PTMD05253P485528204
NRIP1
Nuclear receptor-interacting protein 1
Homo sapiens
PTMD05398P50851987
LRBA
Lipopolysaccharide-responsive and beige-like anchor protein
Homo sapiens
PTMD05430P515301763
DNA2
DNA replication ATP-dependent helicase/nuclease DNA2 [Includes: DNA replication nuclease DNA2 ; DNA replication ATP-dependent helicase DNA2 ]
Homo sapiens
PTMD05456P517873784
KCNQ1
Potassium voltage-gated channel subfamily KQT member 1
Homo sapiens
PTMD05495P522724670
HNRNPM
Heterogeneous nuclear ribonucleoprotein M
Homo sapiens
PTMD05520P527903101
HK3
Hexokinase-3
Homo sapiens
PTMD06110Q01484287
ANK2
Ankyrin-2
Homo sapiens
PTMD06534Q134246640
SNTA1
Alpha-1-syntrophin
Homo sapiens
PTMD06647Q13936775
CACNA1C
Voltage-dependent L-type calcium channel subunit alpha-1C
Homo sapiens
PTMD06676Q141261829
DSG2
Desmoglein-2
Homo sapiens
PTMD07274Q2TB9080201
HKDC1
Hexokinase HKDC1
Homo sapiens
PTMD07694Q5SXM26621
SNAPC4
snRNA-activating protein complex subunit 4
Homo sapiens
PTMD07745Q5T4S723352
UBR4
E3 ubiquitin-protein ligase UBR4
Homo sapiens
PTMD07949Q5ZPR380381
CD276
CD276 antigen
Homo sapiens
PTMD08048Q6DD8825923
ATL3
Atlastin-3
Homo sapiens
PTMD08660Q75QN255656
INTS8
Integrator complex subunit 8
Homo sapiens
PTMD08876Q7Z62810276
NET1
Neuroepithelial cell-transforming gene 1 protein
Homo sapiens
PTMD09015Q86UR522999
RIMS1
Regulating synaptic membrane exocytosis protein 1
Homo sapiens
PTMD09184Q86YD153635
PTOV1
Prostate tumor-overexpressed gene 1 protein
Homo sapiens
PTMD09809Q8N80655148
UBR7
Putative E3 ubiquitin-protein ligase UBR7
Homo sapiens
PTMD11789Q96TA210730
YME1L1
ATP-dependent zinc metalloprotease YME1L1
Homo sapiens
PTMD12658Q9H1V838866
SLC6A17
Sodium-dependent neutral amino acid transporter SLC6A17
Homo sapiens
PTMD12896Q9H7D780232
WDR26
WD repeat-containing protein 26
Homo sapiens
PTMD13477Q9NU2223195
MDN1
Midasin
Homo sapiens
PTMD15060Q9Y6J69992
KCNE2
Potassium voltage-gated channel subfamily E member 2
Homo sapiens