abnormal sensory neuron physiology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any functional anomaly of cells that innervate an effector (muscle or glandular) tissue and are responsible for transmission of sensory impulses (Mammalian Phenotype Ontology, MP_0010055)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010055
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Genes

47 gene mutations causing the abnormal sensory neuron physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADGRV1 adhesion G protein-coupled receptor V1
ALG10 ALG10, alpha-1,2-glucosyltransferase
ATP2B2 ATPase, Ca++ transporting, plasma membrane 2
BSN bassoon presynaptic cytomatrix protein
CACNA1D calcium channel, voltage-dependent, L type, alpha 1D subunit
CDH23 cadherin-related 23
CDKN2D cyclin-dependent kinase inhibitor 2D (p19, inhibits CDK4)
CHD7 chromodomain helicase DNA binding protein 7
CHRNA10 cholinergic receptor, nicotinic, alpha 10 (neuronal)
CHRNA9 cholinergic receptor, nicotinic, alpha 9 (neuronal)
CLRN1 clarin 1
CNGA2 cyclic nucleotide gated channel alpha 2
ESPN espin
FFAR1 free fatty acid receptor 1
FFAR3 free fatty acid receptor 3
FFAR4 free fatty acid receptor 4
GJB6 gap junction protein, beta 6, 30kDa
HPN hepsin
KCNMA1 potassium channel, calcium activated large conductance subfamily M alpha, member 1
KCNQ4 potassium channel, voltage gated KQT-like subfamily Q, member 4
MAGED1 melanoma antigen family D1
MYO1C myosin IC
MYO7A myosin VIIA
OTOF otoferlin
OTOS otospiralin
P2RX2 purinergic receptor P2X, ligand gated ion channel, 2
PAX8 paired box 8
PDZD7 PDZ domain containing 7
PIRT phosphoinositide-interacting regulator of transient receptor potential channels
PSAP prosaposin
PTPRQ protein tyrosine phosphatase, receptor type, Q
SCARB2 scavenger receptor class B, member 2
SDHD succinate dehydrogenase complex, subunit D, integral membrane protein
SLC17A8 solute carrier family 17 (vesicular glutamate transporter), member 8
SLC24A4 solute carrier family 24 (sodium/potassium/calcium exchanger), member 4
SLC26A5 solute carrier family 26 (anion exchanger), member 5
STRC stereocilin
TECTA tectorin alpha
THRB thyroid hormone receptor, beta
TMC1 transmembrane channel-like 1
TMC2 transmembrane channel-like 2
TRIOBP TRIO and F-actin binding protein
TRPA1 transient receptor potential cation channel, subfamily A, member 1
TRPM3 transient receptor potential cation channel, subfamily M, member 3
TRPV1 transient receptor potential cation channel, subfamily V, member 1
USH1C Usher syndrome 1C (autosomal recessive, severe)
USH1G Usher syndrome 1G (autosomal recessive)