curly vibrissae Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description coiled or spiral shape of the stiff hairs that project from the face around the nose of most mammals, and which act as touch receptors (Mammalian Phenotype Ontology, MP_0001274)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001274
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Genes

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

Symbol Name
ACD adrenocortical dysplasia homolog (mouse)
ADAM17 ADAM metallopeptidase domain 17
ATP7A ATPase, Cu++ transporting, alpha polypeptide
ATP7B ATPase, Cu++ transporting, beta polypeptide
C8ORF44-SGK3 C8orf44-SGK3 readthrough
CUX1 cut-like homeobox 1
EGFR epidermal growth factor receptor
ETS2 v-ets avian erythroblastosis virus E26 oncogene homolog 2
FOXN1 forkhead box N1
GATA3 GATA binding protein 3
HR hair growth associated
KRT25 keratin 25, type I
KRT71 keratin 71, type II
MGRN1 mahogunin ring finger 1, E3 ubiquitin protein ligase
MOCS1 molybdenum cofactor synthesis 1
MSX2 msh homeobox 2
PRSS8 protease, serine, 8
SP6 Sp6 transcription factor
TGFA transforming growth factor, alpha
TGM3 transglutaminase 3
TRPV3 transient receptor potential cation channel, subfamily V, member 3