thin interventricular septum Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description decreased thickness of the wall between the two lower chambers of the heart (Mammalian Phenotype Ontology, MP_0010725)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010725
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Genes

15 gene mutations causing the thin interventricular septum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGTR2 angiotensin II receptor, type 2
CAV1 caveolin 1, caveolae protein, 22kDa
EFNA1 ephrin-A1
HOXB4 homeobox B4
KDM6A lysine (K)-specific demethylase 6A
KLK3 kallikrein-related peptidase 3
MEN1 multiple endocrine neoplasia I
MYL2 myosin, light chain 2, regulatory, cardiac, slow
MYLK3 myosin light chain kinase 3
OPA3 optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
PDLIM3 PDZ and LIM domain 3
PPARG peroxisome proliferator-activated receptor gamma
RYR2 ryanodine receptor 2 (cardiac)
SH3PXD2B SH3 and PX domains 2B
TXNRD2 thioredoxin reductase 2