abnormal sinus arrhythmia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the normal phenomenon of mild acceleration and slowing of the heart rate that occurs during the respiratory cycle (Mammalian Phenotype Ontology, MP_0004122)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004122
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14 gene mutations causing the abnormal sinus arrhythmia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADRA1A adrenoceptor alpha 1A
AKAP10 A kinase (PRKA) anchor protein 10
ANK2 ankyrin 2, neuronal
CACNA1D calcium channel, voltage-dependent, L type, alpha 1D subunit
CALCB calcitonin-related polypeptide beta
CASQ2 calsequestrin 2 (cardiac muscle)
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
IDUA iduronidase, alpha-L-
IGHMBP2 immunoglobulin mu binding protein 2
LAMA4 laminin, alpha 4
NHLH1 nescient helix loop helix 1
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
TBX3 T-box 3
TBX5 T-box 5