head bobbing Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description repetitive up and down movement of the head (Mammalian Phenotype Ontology, MP_0001410)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001410
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Genes

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

Symbol Name
ATP2B2 ATPase, Ca++ transporting, plasma membrane 2
BDNF brain-derived neurotrophic factor
CACNG2 calcium channel, voltage-dependent, gamma subunit 2
CARS2 cysteinyl-tRNA synthetase 2, mitochondrial (putative)
CDH23 cadherin-related 23
CELSR1 cadherin, EGF LAG seven-pass G-type receptor 1
CHD7 chromodomain helicase DNA binding protein 7
CLIC5 chloride intracellular channel 5
CLRN1 clarin 1
COL2A1 collagen, type II, alpha 1
DFNB31 deafness, autosomal recessive 31
DRD3 dopamine receptor D3
EFNB2 ephrin-B2
ELMOD1 ELMO/CED-12 domain containing 1
EPHB2 EPH receptor B2
EYA1 EYA transcriptional coactivator and phosphatase 1
GFI1 growth factor independent 1 transcription repressor
GRXCR1 glutaredoxin, cysteine rich 1
JAG1 jagged 1
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
LOC102723475 putative uncharacterized protein LOC388820
MAOA monoamine oxidase A
MIR96 microRNA 96
MYO15A myosin XVA
MYO6 myosin VI
MYO7A myosin VIIA
PCDH15 protocadherin-related 15
PHEX phosphate regulating endopeptidase homolog, X-linked
POU3F4 POU class 3 homeobox 4
POU4F3 POU class 4 homeobox 3
SCN1A sodium channel, voltage gated, type I alpha subunit
SLC12A2 solute carrier family 12 (sodium/potassium/chloride transporter), member 2
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SOX2 SRY (sex determining region Y)-box 2
SPTBN4 spectrin, beta, non-erythrocytic 4
UNC5C unc-5 homolog C (C. elegans)
USH1C Usher syndrome 1C (autosomal recessive, severe)
ZEB1 zinc finger E-box binding homeobox 1