head tossing Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description repetitive flailing of the head in multiple directions (Mammalian Phenotype Ontology, MP_0005307)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005307
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Genes

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

Symbol Name
ATF2 activating transcription factor 2
ATP2B2 ATPase, Ca++ transporting, plasma membrane 2
CACNG2 calcium channel, voltage-dependent, gamma subunit 2
CDH23 cadherin-related 23
CHD7 chromodomain helicase DNA binding protein 7
DFNB31 deafness, autosomal recessive 31
GRXCR1 glutaredoxin, cysteine rich 1
JAG1 jagged 1
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
LHFPL5 lipoma HMGIC fusion partner-like 5
LMX1A LIM homeobox transcription factor 1, alpha
LOC102723475 putative uncharacterized protein LOC388820
LRIG3 leucine-rich repeats and immunoglobulin-like domains 3
LRTOMT leucine rich transmembrane and O-methyltransferase domain containing
MAFB v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog B
MCOLN3 mucolipin 3
MYO6 myosin VI
MYO7A myosin VIIA
PCDH15 protocadherin-related 15
POU4F3 POU class 4 homeobox 3
SCN8A sodium channel, voltage gated, type VIII alpha subunit
SLC12A2 solute carrier family 12 (sodium/potassium/chloride transporter), member 2
SOX2 SRY (sex determining region Y)-box 2
SRRM4 serine/arginine repetitive matrix 4
TBX10 T-box 10
TMC1 transmembrane channel-like 1
USH1C Usher syndrome 1C (autosomal recessive, severe)
USH1G Usher syndrome 1G (autosomal recessive)