vascular smooth muscle cell hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description decreased numbers of smooth muscle cells in the vascular wall (Mammalian Phenotype Ontology, MP_0003814)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003814
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Genes

13 gene mutations causing the vascular smooth muscle cell hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CALCRL calcitonin receptor-like
HHEX hematopoietically expressed homeobox
LMNA lamin A/C
LPAR4 lysophosphatidic acid receptor 4
MKL2 MKL/myocardin-like 2
NRP1 neuropilin 1
PROS1 protein S (alpha)
PTPRJ protein tyrosine phosphatase, receptor type, J
RAPGEF1 Rap guanine nucleotide exchange factor (GEF) 1
S1PR1 sphingosine-1-phosphate receptor 1
SHC1 SHC (Src homology 2 domain containing) transforming protein 1
TBX1 T-box 1
ZFAND5 zinc finger, AN1-type domain 5