abnormal b wave amplitude Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the size (height or maximum displacement) of the b wave as measured in the electroretinogram (Mammalian Phenotype Ontology, MP_0012031)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012031
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11 gene mutations causing the abnormal b wave amplitude phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADRB2 adrenoceptor beta 2, surface
CACNA1F calcium channel, voltage-dependent, L type, alpha 1F subunit
CFH complement factor H
GLRA1 glycine receptor, alpha 1
KL klotho
MT-ND6 NADH dehydrogenase, subunit 6 (complex I)
PROM1 prominin 1
RHO rhodopsin
RP1 retinitis pigmentosa 1 (autosomal dominant)
TSHR thyroid stimulating hormone receptor
TYR tyrosinase