absent heartbeat Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description lack of a spontaneously beating heart (usually due to defects in the calcium delivery mechanism or loss of a functional contractile apparatus) (Mammalian Phenotype Ontology, MP_0004086)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004086
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22 gene mutations causing the absent heartbeat phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARID1A AT rich interactive domain 1A (SWI-like)
CSNK2A1 casein kinase 2, alpha 1 polypeptide
CXADR coxsackie virus and adenovirus receptor
EGFL7 EGF-like-domain, multiple 7
ENG endoglin
ETV2 ets variant 2
F2R coagulation factor II (thrombin) receptor
FHOD3 formin homology 2 domain containing 3
FOXO1 forkhead box O1
HSP90AB1 heat shock protein 90kDa alpha (cytosolic), class B member 1
IKBKAP inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
KAT7 K(lysine) acetyltransferase 7
PINX1 PIN2/TERF1 interacting, telomerase inhibitor 1
PTK2 protein tyrosine kinase 2
RYR2 ryanodine receptor 2 (cardiac)
SLC8A1 solute carrier family 8 (sodium/calcium exchanger), member 1
SP4 Sp4 transcription factor
TMED2 transmembrane emp24 domain trafficking protein 2
TMOD1 tropomodulin 1
TNNT2 troponin T type 2 (cardiac)
TTN titin
WASL Wiskott-Aldrich syndrome-like