abnormal susceptibility to hearing loss Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the sensitivity to loss of hearing related to age or environmental factors (Mammalian Phenotype Ontology, MP_0006334)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006334
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Genes

31 gene mutations causing the abnormal susceptibility to hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1
ACTG1 actin gamma 1
ADGRV1 adhesion G protein-coupled receptor V1
ATP2B2 ATPase, Ca++ transporting, plasma membrane 2
BARHL1 BarH-like homeobox 1
CDH23 cadherin-related 23
CHRNA9 cholinergic receptor, nicotinic, alpha 9 (neuronal)
COL1A1 collagen, type I, alpha 1
CS citrate synthase
DMD dystrophin
FBXO2 F-box protein 2
FIGN fidgetin
FSCN2 fascin actin-bundling protein 2, retinal
GJC3 gap junction protein, gamma 3, 30.2kDa
GPX1 glutathione peroxidase 1
GRID1 glutamate receptor, ionotropic, delta 1
KCNMA1 potassium channel, calcium activated large conductance subfamily M alpha, member 1
LRP2 low density lipoprotein receptor-related protein 2
MYD88 myeloid differentiation primary response 88
MYH9 myosin, heavy chain 9, non-muscle
MYO7A myosin VIIA
NDP Norrie disease (pseudoglioma)
NFKB1 nuclear factor of kappa light polypeptide gene enhancer in B-cells 1
NGFR nerve growth factor receptor
OPRL1 opiate receptor-like 1
PARP1 poly (ADP-ribose) polymerase 1
POLG polymerase (DNA directed), gamma
SLC1A3 solute carrier family 1 (glial high affinity glutamate transporter), member 3
SOD1 superoxide dismutase 1, soluble
TNFRSF11B tumor necrosis factor receptor superfamily, member 11b
TRPV4 transient receptor potential cation channel, subfamily V, member 4