head shaking Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description repetitive movement of the head in the horizontal plane (Mammalian Phenotype Ontology, MP_0002730)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002730
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Genes

20 gene mutations causing the head shaking phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATF2 activating transcription factor 2
CACNG2 calcium channel, voltage-dependent, gamma subunit 2
CDH23 cadherin-related 23
CELSR1 cadherin, EGF LAG seven-pass G-type receptor 1
CHD7 chromodomain helicase DNA binding protein 7
ESPN espin
FIGN fidgetin
JAG1 jagged 1
LHFPL5 lipoma HMGIC fusion partner-like 5
MYO6 myosin VI
MYO7A myosin VIIA
OTX1 orthodenticle homeobox 1
POU3F4 POU class 3 homeobox 4
PSAP prosaposin
SIX1 SIX homeobox 1
TMIE transmembrane inner ear
TTPA tocopherol (alpha) transfer protein
USH1G Usher syndrome 1G (autosomal recessive)
VANGL2 VANGL planar cell polarity protein 2
ZEB1 zinc finger E-box binding homeobox 1