abnormal interventricular septum thickness Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description an anomaly in the thickness of the wall between the two lower chambers of the heart compared to the control (Mammalian Phenotype Ontology, MP_0020136)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0020136
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Genes

36 gene mutations causing the abnormal interventricular septum thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABL1 ABL proto-oncogene 1, non-receptor tyrosine kinase
AGTR2 angiotensin II receptor, type 2
CAV1 caveolin 1, caveolae protein, 22kDa
CAV3 caveolin 3
EFNA1 ephrin-A1
FKBP1B FK506 binding protein 1B, 12.6 kDa
GATA5 GATA binding protein 5
HDAC2 histone deacetylase 2
HEXIM1 hexamethylene bis-acetamide inducible 1
HOXB4 homeobox B4
HSPB8 heat shock 22kDa protein 8
IDUA iduronidase, alpha-L-
IGF2R insulin-like growth factor 2 receptor
INS insulin
KDM6A lysine (K)-specific demethylase 6A
KLK3 kallikrein-related peptidase 3
LBX1 ladybird homeobox 1
MEN1 multiple endocrine neoplasia I
MMP9 matrix metallopeptidase 9
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)
PAX3 paired box 3
PDLIM3 PDZ and LIM domain 3
PEPD peptidase D
PNPLA2 patatin-like phospholipase domain containing 2
PPARG peroxisome proliferator-activated receptor gamma
PTPN11 protein tyrosine phosphatase, non-receptor type 11
RAF1 Raf-1 proto-oncogene, serine/threonine kinase
RYR2 ryanodine receptor 2 (cardiac)
SH3PXD2B SH3 and PX domains 2B
SLC39A4 solute carrier family 39 (zinc transporter), member 4
SOS1 son of sevenless homolog 1 (Drosophila)
SOX4 SRY (sex determining region Y)-box 4
TNNI3 troponin I type 3 (cardiac)
TXNRD2 thioredoxin reductase 2