bidirectional circling Gene Set
Genes
22 gene mutations causing the bidirectional circling phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol |
Name |
|
CDH23
|
cadherin-related 23
|
|
CHD7
|
chromodomain helicase DNA binding protein 7
|
|
CLIC5
|
chloride intracellular channel 5
|
|
CYCS
|
cytochrome c, somatic
|
|
ESPN
|
espin
|
|
FIGN
|
fidgetin
|
|
GRXCR1
|
glutaredoxin, cysteine rich 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
|
|
LRTOMT
|
leucine rich transmembrane and O-methyltransferase domain containing
|
|
MYO6
|
myosin VI
|
|
NR4A3
|
nuclear receptor subfamily 4, group A, member 3
|
|
PCDH15
|
protocadherin-related 15
|
|
SOBP
|
sine oculis binding protein homolog (Drosophila)
|
|
SOX2
|
SRY (sex determining region Y)-box 2
|
|
TBX1
|
T-box 1
|
|
TBX10
|
T-box 10
|
|
TMIE
|
transmembrane inner ear
|
|
USH1G
|
Usher syndrome 1G (autosomal recessive)
|
|
ZEB1
|
zinc finger E-box binding homeobox 1
|
