short vibrissae Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description decreased length of the stiff hairs projecting from the face around the nose of most mammals which act as touch receptors (Mammalian Phenotype Ontology, MP_0001282)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001282
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Genes

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

Symbol Name
ACD adrenocortical dysplasia homolog (mouse)
ADAM17 ADAM metallopeptidase domain 17
BARX2 BARX homeobox 2
CTSV cathepsin V
CUX1 cut-like homeobox 1
DSG4 desmoglein 4
EGFR epidermal growth factor receptor
FOXN1 forkhead box N1
GATA3 GATA binding protein 3
GTF2IRD1 GTF2I repeat domain containing 1
HR hair growth associated
LBR lamin B receptor
MSX2 msh homeobox 2
ORAI1 ORAI calcium release-activated calcium modulator 1
POU3F4 POU class 3 homeobox 4
PRSS8 protease, serine, 8
SOX18 SRY (sex determining region Y)-box 18
SP6 Sp6 transcription factor