Disease: hearing impairment
Source: ALL
Gene Uniprot Gene Full Name Protein Class pLI DSI v DPI v
DFNA24 deafness, autosomal dominant 24 0.931 0.115
CABP2 Q9NPB3 calcium binding protein 2 2.5E-03 0.861 0.115
TMIE Q8NEW7 transmembrane inner ear 7.7E-05 0.890 0.115
TPRN Q4KMQ1 taperin 7.2E-03 0.839 0.115
DFNB38 deafness, autosomal recessive 38 1.000 0.115
GJC3 Q8NFK1 gap junction protein gamma 3 5.3E-04 1.000 0.115
GRXCR1 A8MXD5 glutaredoxin and cysteine rich domain containing 1 3.9E-11 0.861 0.115
PJVK Q0ZLH3 pejvakin 3.7E-08 0.769 0.115
DFNX3 deafness, X-linked 3 0.861 0.192
SMIM12 Q96EX1 small integral membrane protein 12 0.57 0.780 0.192
STRC Q7RTU9 stereocilin Extracellular structure 1.8E-15 0.700 0.192
LRTOMT Q8WZ04 Q96E66 leucine rich transmembrane and O-methyltransferase domain containing Enzyme 7.0E-05 0.792 0.192
LHFPL5 Q8TAF8 LHFPL tetraspan subfamily member 5 4.0E-04 0.861 0.192
CEACAM16 Q2WEN9 CEA cell adhesion molecule 16, tectorial membrane component 1.6E-05 0.805 0.192
EPS8L2 Q9H6S3 EPS8 like 2 Receptor 1.5E-06 0.890 0.231
LOXHD1 Q8IVV2 lipoxygenase homology domains 1 5.6E-26 0.792 0.231
GIPC3 Q8TF64 GIPC PDZ domain containing family member 3 Enzyme 9.3E-03 0.780 0.231
OTOG Q6ZRI0 otogelin 6.6E-37 0.805 0.231
MYO1A Q9UBC5 myosin IA Cellular structure 8.9E-46 0.769 0.269
TRIOBP Q9H2D6 TRIO and F-actin binding protein Enzyme modulator 2.0E-28 0.743 0.269
MYO3A Q8NEV4 myosin IIIA Kinase 1.8E-45 0.780 0.269
ELMOD3 Q96FG2 ELMO domain containing 3 Signaling 5.0E-16 0.821 0.269
OTOGL Q3ZCN5 otogelin like Enzyme modulator 4.7E-52 0.805 0.269
MSRB3 Q8IXL7 methionine sulfoxide reductase B3 3.8E-03 0.729 0.308
CRYM Q14894 crystallin mu Enzyme 2.6E-02 0.769 0.346