sinoatrial block Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	Disturbance in the atrial activation that is caused by transient failure of impulse conduction from the sinoatrial node to the cardiac atria. (Human Phenotype Ontology, HP_0012723)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010520
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Genes

12 gene mutations causing the sinoatrial block phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
DMD	dystrophin
GJA1	gap junction protein, alpha 1, 43kDa
GJA5	gap junction protein, alpha 5, 40kDa
HCN4	hyperpolarization activated cyclic nucleotide gated potassium channel 4
HOPX	HOP homeobox
IDUA	iduronidase, alpha-L-
IGHMBP2	immunoglobulin mu binding protein 2
LMNA	lamin A/C
SCN5A	sodium channel, voltage gated, type V alpha subunit
SLC2A8	solute carrier family 2 (facilitated glucose transporter), member 8
SP4	Sp4 transcription factor
TBX5	T-box 5