| IFNA1 |
P01562
|
interferon alpha 1
|
|
|
0.371 |
0.923 |
| IFNA13 |
P01562
|
interferon alpha 13
|
|
|
0.374 |
0.923 |
| HTC2 |
|
hypertrichosis 2 (generalized, congenital)
|
|
|
0.392 |
0.808 |
| PWAR1 |
|
Prader Willi/Angelman region RNA 1
|
|
|
0.490 |
0.769 |
| H19 |
|
H19 imprinted maternally expressed transcript
|
|
|
0.494 |
0.923 |
| HPT |
|
hypoparathyroidism
|
|
|
0.593 |
0.692 |
| PWRN1 |
|
Prader-Willi region non-protein coding RNA 1
|
|
|
0.670 |
0.500 |
| NPAP1 |
Q9NZP6
|
nuclear pore associated protein 1
|
Nucleic acid binding
|
|
0.670 |
0.500 |
| SNORD116-1 |
|
small nucleolar RNA, C/D box 116-1
|
|
|
0.682 |
0.423 |
| MKRN3-AS1 |
|
MKRN3 antisense RNA 1
|
|
|
0.682 |
0.423 |
| SNORD115-1 |
|
small nucleolar RNA, C/D box 115-1
|
|
|
0.682 |
0.423 |
| IPW |
|
imprinted in Prader-Willi syndrome
|
|
|
0.682 |
0.423 |
| IGHD |
P01880
|
immunoglobulin heavy constant delta
|
|
|
0.722 |
0.346 |
| ALMS1 |
Q8TCU4
|
ALMS1 centrosome and basal body associated protein
|
|
4.5E-60 |
0.559 |
0.808 |
| VPS13B |
Q7Z7G8
|
vacuolar protein sorting 13 homolog B
|
|
2.5E-45 |
0.579 |
0.769 |
| FANCI |
Q9NVI1
|
FA complementation group I
|
|
8.9E-37 |
0.543 |
0.731 |
| IFT172 |
Q9UG01
|
intraflagellar transport 172
|
Cellular structure
|
3.3E-33 |
0.582 |
0.654 |
| KIAA0556 |
O60303
|
KIAA0556
|
|
1.2E-29 |
0.644 |
0.538 |
| KIAA0753 |
Q2KHM9
|
KIAA0753
|
|
1.6E-28 |
0.631 |
0.577 |
| POLE |
Q07864
|
DNA polymerase epsilon, catalytic subunit
|
|
8.0E-27 |
0.526 |
0.731 |
| OBSL1 |
O75147
|
obscurin like cytoskeletal adaptor 1
|
|
1.0E-25 |
0.686 |
0.308 |
| TMEM67 |
Q5HYA8
|
transmembrane protein 67
|
|
2.1E-24 |
0.512 |
0.769 |
| POLR3A |
O14802
|
RNA polymerase III subunit A
|
Enzyme
|
1.3E-23 |
0.538 |
0.769 |
| CLCNKB |
P51801
|
chloride voltage-gated channel Kb
|
Ion channel
|
1.4E-22 |
0.593 |
0.692 |
| CUL7 |
Q14999
|
cullin 7
|
|
2.6E-21 |
0.633 |
0.500 |