| GUSBP14 |
|
GUSB pseudogene 14
|
|
|
0.839 |
0.077 |
| GUSBP3 |
|
GUSB pseudogene 3
|
|
|
0.861 |
0.077 |
| GUSBP1 |
Q15486
|
GUSB pseudogene 1
|
|
|
0.861 |
0.077 |
| CMTX2 |
|
Charcot-Marie-Tooth neuropathy, X-linked 2 (recessive)
|
|
|
1.000 |
0.077 |
| TEKT3 |
Q9BXF9
|
tektin 3
|
Cellular structure
|
2.0E-17 |
1.000 |
0.077 |
| C1orf194 |
Q5T5A4
|
chromosome 1 open reading frame 194
|
|
4.0E-06 |
0.792 |
0.115 |
| DRP2 |
Q13474
|
dystrophin related protein 2
|
|
3.7E-06 |
0.805 |
0.115 |
| MBS2 |
|
Moebius syndrome 2
|
|
|
0.931 |
0.115 |
| D1S111 |
|
Minisatellite 33.6
|
|
|
0.931 |
0.115 |
| COX6A1 |
P12074
|
cytochrome c oxidase subunit 6A1
|
Enzyme
|
2.3E-03 |
0.780 |
0.154 |
| GLC3B |
|
glaucoma 3, primary infantile, B
|
|
|
0.769 |
0.154 |
| DCTN2 |
Q13561
|
dynactin subunit 2
|
Cellular structure
|
1.00 |
0.805 |
0.154 |
| CMTX3 |
|
Charcot-Marie-Tooth neuropathy, X-linked 3 (dominant)
|
|
|
0.821 |
0.154 |
| DFNA7 |
|
deafness, autosomal dominant 7
|
|
|
0.861 |
0.154 |
| DFNA49 |
|
deafness, autosomal dominant 49
|
|
|
0.861 |
0.154 |
| DNAJB2 |
P25686
|
DnaJ heat shock protein family (Hsp40) member B2
|
|
5.4E-05 |
0.743 |
0.192 |
| PXMP2 |
Q9NR77
|
peroxisomal membrane protein 2
|
Receptor
|
9.2E-03 |
0.743 |
0.192 |
| PMP2 |
P02689
|
peripheral myelin protein 2
|
|
8.5E-03 |
0.769 |
0.231 |
| LRIG3 |
Q6UXM1
|
leucine rich repeats and immunoglobulin like domains 3
|
Receptor
|
1.2E-09 |
0.743 |
0.231 |
| RER1 |
O15258
|
retention in endoplasmic reticulum sorting receptor 1
|
|
0.38 |
0.821 |
0.231 |
| PLEKHM3 |
Q6ZWE6
|
pleckstrin homology domain containing M3
|
|
1.0E-04 |
0.861 |
0.231 |
| PRB4 |
P10163
|
proline rich protein BstNI subfamily 4
|
|
1.3E-09 |
0.861 |
0.231 |
| JPH1 |
Q9HDC5
|
junctophilin 1
|
|
0.77 |
0.705 |
0.269 |
| MYO1A |
Q9UBC5
|
myosin IA
|
Cellular structure
|
8.9E-46 |
0.769 |
0.269 |
| SLC25A46 |
Q96AG3
|
solute carrier family 25 member 46
|
Transporter
|
1.3E-05 |
0.695 |
0.308 |