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Træk

Complete right bundle branch block

A conduction block of the right branch of the bundle of His. This manifests as a prolongation of the QRS complex (greater than 0.12 s) with delayed activation of the right ventricle and terminal delay on the EKG.

HPO HP:0011712

Resumé

Også kaldet
Right bundle branch block, Right bundle-branch block
Kropssystem
Abnormality of the cardiovascular system

58 gener knyttet til Complete right bundle branch block

Ændringer i disse gener forårsager sjældne tilstande, hvor Complete right bundle branch block ses. De fleste med dette træk har ingen af disse tilstande, og et gen på denne liste siger intet om nogens eget genom.

GenHvor ofte det sesTilstande
BANF1barrier to autointegration nuclear assembly factor 1AltidI 1 tilstand
CNBPCCHC-type zinc finger nucleic acid binding proteinAltidI 1 tilstand
EXOSC5exosome component 5AltidI 1 tilstand
GYG1glycogenin 1AltidI 2 tilstande
HCN4hyperpolarization activated cyclic nucleotide gated potassium channel 4AltidI 2 tilstande
LMOD2leiomodin 2AltidI 1 tilstand
MYH6myosin heavy chain 6AltidI 1 tilstand
POMT2protein O-mannosyltransferase 2AltidI 2 tilstande
TNNC1troponin C1, slow skeletal and cardiac typeAltidI 1 tilstand
ABCC9ATP binding cassette subfamily C member 9Ofte (30–79 %)I 1 tilstand
AKAP9A-kinase anchoring protein 9Ofte (30–79 %)I 1 tilstand
CACNA1Ccalcium voltage-gated channel subunit alpha1 COfte (30–79 %)I 1 tilstand
CACNA2D1calcium voltage-gated channel auxiliary subunit alpha2delta 1Ofte (30–79 %)I 1 tilstand
CACNB2calcium voltage-gated channel auxiliary subunit beta 2Ofte (30–79 %)I 1 tilstand
DNMT3BDNA methyltransferase 3 betaOfte (30–79 %)I 1 tilstand
DUX4double homeobox 4Ofte (30–79 %)I 1 tilstand
DUX4L1double homeobox 4 like 1 (pseudogene)Ofte (30–79 %)I 1 tilstand
FRG1FSHD region gene 1Ofte (30–79 %)I 1 tilstand
GPD1Lglycerol-3-phosphate dehydrogenase 1 likeOfte (30–79 %)I 2 tilstande
KCND3potassium voltage-gated channel subfamily D member 3Ofte (30–79 %)I 1 tilstand
KCNE3potassium voltage-gated channel subfamily E regulatory subunit 3Ofte (30–79 %)I 1 tilstand
KCNE5potassium voltage-gated channel subfamily E regulatory subunit 5Ofte (30–79 %)I 1 tilstand
KCNJ8potassium inwardly rectifying channel subfamily J member 8Ofte (30–79 %)I 1 tilstand
LEMD2LEM domain nuclear envelope protein 2Ofte (30–79 %)I 1 tilstand
MYH7myosin heavy chain 7Ofte (30–79 %)I 2 tilstande
NPPAnatriuretic peptide AOfte (30–79 %)I 1 tilstand
PKP2plakophilin 2Ofte (30–79 %)I 1 tilstand
PPP1CBprotein phosphatase 1 catalytic subunit betaOfte (30–79 %)I 1 tilstand
RANGRFRAN guanine nucleotide release factorOfte (30–79 %)I 1 tilstand
SCN10Asodium voltage-gated channel alpha subunit 10Ofte (30–79 %)I 1 tilstand
SCN1Bsodium voltage-gated channel beta subunit 1Ofte (30–79 %)I 1 tilstand
SCN2Bsodium voltage-gated channel beta subunit 2Ofte (30–79 %)I 1 tilstand
SCN3Bsodium voltage-gated channel beta subunit 3Ofte (30–79 %)I 1 tilstand
SCN5Asodium voltage-gated channel alpha subunit 5Ofte (30–79 %)I 5 tilstande
SCNN1Asodium channel epithelial 1 subunit alphaOfte (30–79 %)I 1 tilstand
SEMA3Asemaphorin 3AOfte (30–79 %)I 1 tilstand
SLMAPsarcolemma associated proteinOfte (30–79 %)I 1 tilstand
SMCHD1structural maintenance of chromosomes flexible hinge domain containing 1Ofte (30–79 %)I 1 tilstand
TLL1tolloid like 1Ofte (30–79 %)I 1 tilstand
TRPM4transient receptor potential cation channel subfamily M member 4Ofte (30–79 %)I 2 tilstande
Vis 18 gener mere
GenHvor ofte det sesTilstande
ACTC1actin alpha cardiac muscle 1Nogle gange (5–29 %)I 1 tilstand
CITED2Cbp/p300 interacting transactivator with ED-rich tail 2Nogle gange (5–29 %)I 1 tilstand
DSG2desmoglein 2Nogle gange (5–29 %)I 1 tilstand
DYSFdysferlinNogle gange (5–29 %)I 1 tilstand
FHL1four and a half LIM domains 1Nogle gange (5–29 %)I 1 tilstand
FLNCfilamin CNogle gange (5–29 %)I 1 tilstand
KCNK3potassium two pore domain channel subfamily K member 3Nogle gange (5–29 %)I 1 tilstand
MT-CYBmitochondrially encoded cytochrome bNogle gange (5–29 %)I 1 tilstand
PIGUphosphatidylinositol glycan anchor biosynthesis class UNogle gange (5–29 %)I 1 tilstand
RNASEH1ribonuclease H1Nogle gange (5–29 %)I 1 tilstand
SOX17SRY-box transcription factor 17Nogle gange (5–29 %)I 1 tilstand
TNNT2troponin T2, cardiac typeNogle gange (5–29 %)I 1 tilstand
PLECplectinSjældent (1–4%)I 1 tilstand
ATP6V1E1ATPase H+ transporting V1 subunit E1Ikke registreretI 1 tilstand
GNAI2G protein subunit alpha i2Ikke registreretI 1 tilstand
JUPjunction plakoglobinIkke registreretI 1 tilstand
MYBPC3myosin binding protein C3Ikke registreretI 1 tilstand
TNNI3KTNNI3 interacting kinaseIkke registreretI 1 tilstand

Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.

Bredere træk

Bundle branch block

Hvor oplysningerne kommer fra

  • Human Phenotype Ontology, udgivelse 2026-09-01: egenskaben, dens navne, definition og de gener, der er knyttet til den. Læs mere på hpo.jax.org.
  • Dataudgivelse 2026.10.17-8666dff2.

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