sparse vibrissae Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description few and widely spaced stiff hairs that project from the face around the nose of most mammals, and which act as touch receptors (Mammalian Phenotype Ontology, MP_0001283)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001283
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Genes

6 gene mutations causing the sparse vibrissae phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
CTSV cathepsin V
FOXN1 forkhead box N1
GTF2IRD1 GTF2I repeat domain containing 1
SPINK5 serine peptidase inhibitor, Kazal type 5
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor