absent vibrissae Gene Set
Genes
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
|
