abnormal vestibular saccule morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the smaller of the two sacs in the vestibule (Mammalian Phenotype Ontology, MP_0006089)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006089
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Genes

44 gene mutations causing the abnormal vestibular saccule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATF2 activating transcription factor 2
ATG4B autophagy related 4B, cysteine peptidase
ATP2B2 ATPase, Ca++ transporting, plasma membrane 2
CDH23 cadherin-related 23
DLX5 distal-less homeobox 5
ESPN espin
EYA1 EYA transcriptional coactivator and phosphatase 1
FGF10 fibroblast growth factor 10
FGF3 fibroblast growth factor 3
FOXI1 forkhead box I1
GATA3 GATA binding protein 3
GBX2 gastrulation brain homeobox 2
GRXCR1 glutaredoxin, cysteine rich 1
HES1 hes family bHLH transcription factor 1
HES5 hes family bHLH transcription factor 5
HMX2 H6 family homeobox 2
HMX3 H6 family homeobox 3
HOXA1 homeobox A1
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
LMX1A LIM homeobox transcription factor 1, alpha
LOC102723475 putative uncharacterized protein LOC388820
MITF microphthalmia-associated transcription factor
MYO6 myosin VI
MYO7A myosin VIIA
OC90 otoconin 90
OTOG otogelin
OTX1 orthodenticle homeobox 1
PAX2 paired box 2
PAX3 paired box 3
PCDH15 protocadherin-related 15
PHEX phosphate regulating endopeptidase homolog, X-linked
S1PR2 sphingosine-1-phosphate receptor 2
SHH sonic hedgehog
SIX1 SIX homeobox 1
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
TBX10 T-box 10
TMC1 transmembrane channel-like 1
TMIE transmembrane inner ear
TMPRSS3 transmembrane protease, serine 3
USH1G Usher syndrome 1G (autosomal recessive)