abnormal heart shape Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the characteristic surface outline or contour of the heart (Mammalian Phenotype Ontology, MP_0000277)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000277
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17 gene mutations causing the abnormal heart shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATP2A2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2
GAA glucosidase, alpha; acid
GJA1 gap junction protein, alpha 1, 43kDa
HEXIM1 hexamethylene bis-acetamide inducible 1
HEY2 hes-related family bHLH transcription factor with YRPW motif 2
ISL1 ISL LIM homeobox 1
MYH10 myosin, heavy chain 10, non-muscle
NF1 neurofibromin 1
NKX2-5 NK2 homeobox 5
NTRK3 neurotrophic tyrosine kinase, receptor, type 3
SH3PXD2B SH3 and PX domains 2B
SLC4A1 solute carrier family 4 (anion exchanger), member 1 (Diego blood group)
SPTAN1 spectrin, alpha, non-erythrocytic 1
TCF21 transcription factor 21
WT1 Wilms tumor 1
XIRP2 xin actin binding repeat containing 2
ZFPM2 zinc finger protein, FOG family member 2