absent vibrissae Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence 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_0001284)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001284
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21 gene mutations causing the absent vibrissae phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATP7A ATPase, Cu++ transporting, alpha polypeptide
CHUK conserved helix-loop-helix ubiquitous kinase
CTSV cathepsin V
DSG4 desmoglein 4
EDA ectodysplasin A
EGFR epidermal growth factor receptor
FOXI3 forkhead box I3
FOXN1 forkhead box N1
HOXC13 homeobox C13
INHBA inhibin, beta A
IRF6 interferon regulatory factor 6
KRT17 keratin 17, type I
LEF1 lymphoid enhancer-binding factor 1
PRSS8 protease, serine, 8
RIPK4 receptor-interacting serine-threonine kinase 4
SCNN1B sodium channel, non voltage gated 1 beta subunit
SLC52A2 solute carrier family 52 (riboflavin transporter), member 2
SP6 Sp6 transcription factor
ST14 suppression of tumorigenicity 14 (colon carcinoma)
TP63 tumor protein p63
TRPS1 trichorhinophalangeal syndrome I