abnormal vestibular ganglion morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the group of neurons associated with the vestibular part of the eighth cranial nerve that are involved in equilibration (Mammalian Phenotype Ontology, MP_0002856)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002856
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24 gene mutations causing the abnormal vestibular ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARSA arylsulfatase A
ATF2 activating transcription factor 2
BDNF brain-derived neurotrophic factor
EYA1 EYA transcriptional coactivator and phosphatase 1
GABRB3 gamma-aminobutyric acid (GABA) A receptor, beta 3
GRXCR1 glutaredoxin, cysteine rich 1
HOXA1 homeobox A1
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
MAN2B1 mannosidase, alpha, class 2B, member 1
MCOLN3 mucolipin 3
MYO6 myosin VI
MYO7A myosin VIIA
NTF4 neurotrophin 4
NTRK2 neurotrophic tyrosine kinase, receptor, type 2
NTRK3 neurotrophic tyrosine kinase, receptor, type 3
OTOP1 otopetrin 1
PAX2 paired box 2
POU4F1 POU class 4 homeobox 1
POU4F3 POU class 4 homeobox 3
SCUBE1 signal peptide, CUB domain, EGF-like 1
SLC9A1 solute carrier family 9, subfamily A (NHE1, cation proton antiporter 1), member 1
SLITRK6 SLIT and NTRK-like family, member 6
TBX10 T-box 10
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)