abnormal atrioventricular conduction Gene Set
Genes
19 genes associated with the abnormal atrioventricular conduction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
AGXT
|
alanine-glyoxylate aminotransferase
|
|
CTNNA3
|
catenin (cadherin-associated protein), alpha 3
|
|
DMPK
|
dystrophia myotonica-protein kinase
|
|
EMD
|
emerin
|
|
GJA1
|
gap junction protein, alpha 1, 43kDa
|
|
GJA5
|
gap junction protein, alpha 5, 40kDa
|
|
GPD1L
|
glycerol-3-phosphate dehydrogenase 1-like
|
|
GYG1
|
glycogenin 1
|
|
KCNJ5
|
potassium channel, inwardly rectifying subfamily J, member 5
|
|
LMNA
|
lamin A/C
|
|
MYOZ2
|
myozenin 2
|
|
POMT2
|
protein-O-mannosyltransferase 2
|
|
PRKAG2
|
protein kinase, AMP-activated, gamma 2 non-catalytic subunit
|
|
PTPN11
|
protein tyrosine phosphatase, non-receptor type 11
|
|
SCN1B
|
sodium channel, voltage gated, type I beta subunit
|
|
SCN4B
|
sodium channel, voltage gated, type IV beta subunit
|
|
SCN5A
|
sodium channel, voltage gated, type V alpha subunit
|
|
SLC25A20
|
solute carrier family 25 (carnitine/acylcarnitine translocase), member 20
|
|
TRPM4
|
transient receptor potential cation channel, subfamily M, member 4
|
