Disease: Sensorineural Hearing Loss (disorder)
Source: INFERRED ×
Gene Uniprot Gene Full Name Protein Class pLI DSI v DPI v
AAAS Q9NRG9 aladin WD repeat nucleoporin 2.4E-13 0.601 0.654
AARS1 P49588 alanyl-tRNA synthetase 1 Nucleic acid binding 1.8E-08 0.647 0.462
ABHD5 Q8WTS1 abhydrolase domain containing 5 6.4E-07 0.641 0.538
ACOX1 Q15067 acyl-CoA oxidase 1 Enzyme 6.2E-02 0.610 0.731
ACTB P60709 actin beta Cellular structure 0.99 0.325 0.923
ACY1 Q03154 aminoacylase 1 6.9E-09 0.653 0.577
AHI1 Q8N157 Abelson helper integration site 1 1.1E-25 0.513 0.846
AIFM1 O95831 apoptosis inducing factor mitochondria associated 1 Enzyme 1.00 0.527 0.769
ALDH18A1 P54886 aldehyde dehydrogenase 18 family member A1 Enzyme 8.1E-04 0.551 0.769
ALG12 Q9BV10 ALG12 alpha-1,6-mannosyltransferase Enzyme 1.2E-07 0.705 0.500
AMMECR1 Q9Y4X0 AMMECR nuclear protein 1 0.82 0.659 0.692
AP1S2 P56377 adaptor related protein complex 1 subunit sigma 2 Transporter 0.87 0.631 0.615
ARID1B Q8NFD5 AT-rich interaction domain 1B 1.00 0.503 0.846
ARL3 P36405 ADP ribosylation factor like GTPase 3 1.4E-03 0.603 0.615
ARNT2 Q9HBZ2 aryl hydrocarbon receptor nuclear translocator 2 Transcription factor 0.99 0.599 0.731
ASAH1 Q13510 N-acylsphingosine amidohydrolase 1 Enzyme 1.3E-12 0.526 0.808
ATP1A3 P13637 ATPase Na+/K+ transporting subunit alpha 3 Transporter 1.00 0.544 0.615
ATP6 P00846 ATP synthase F0 subunit 6 Transporter 0.541 0.731
ATRX P46100 ATRX chromatin remodeler 1.00 0.452 0.808
BBS2 Q9BXC9 Bardet-Biedl syndrome 2 1.0E-17 0.565 0.654
BCAP31 P51572 B cell receptor associated protein 31 Transporter 0.43 0.579 0.808
BCOR Q6W2J9 BCL6 corepressor 1.00 0.471 0.808
BCR P11274 BCR activator of RhoGEF and GTPase Enzyme modulator 0.99 0.431 0.885
BCS1L Q9Y276 BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone 4.7E-13 0.534 0.808
BMP4 P12644 bone morphogenetic protein 4 Signaling 0.96 0.422 0.808