| IPW |
|
imprinted in Prader-Willi syndrome
|
|
|
0.682 |
0.423 |
| WHCR |
|
Wolf-Hirschhorn syndrome chromosome region
|
|
|
0.638 |
0.577 |
| MKRN3-AS1 |
|
MKRN3 antisense RNA 1
|
|
|
0.682 |
0.423 |
| NPAP1 |
Q9NZP6
|
nuclear pore associated protein 1
|
Nucleic acid binding
|
|
0.670 |
0.500 |
| TTC25 |
Q96NG3
|
tetratricopeptide repeat domain 25
|
|
|
0.674 |
0.538 |
| PWAR1 |
|
Prader Willi/Angelman region RNA 1
|
|
|
0.490 |
0.769 |
| SNORD115-1 |
|
small nucleolar RNA, C/D box 115-1
|
|
|
0.682 |
0.423 |
| PWRN1 |
|
Prader-Willi region non-protein coding RNA 1
|
|
|
0.670 |
0.500 |
| SNORD116-1 |
|
small nucleolar RNA, C/D box 116-1
|
|
|
0.682 |
0.423 |
| FANCA |
O15360
|
FA complementation group A
|
|
1.6E-68 |
0.505 |
0.731 |
| DNAH5 |
Q8TE73
|
dynein axonemal heavy chain 5
|
Enzyme
|
4.9E-64 |
0.590 |
0.692 |
| DNAH11 |
Q96DT5
|
dynein axonemal heavy chain 11
|
Enzyme
|
2.5E-58 |
0.587 |
0.692 |
| PCNT |
O95613
|
pericentrin
|
|
4.0E-58 |
0.564 |
0.808 |
| IFIH1 |
Q9BYX4
|
interferon induced with helicase C domain 1
|
|
7.0E-44 |
0.471 |
0.808 |
| FANCI |
Q9NVI1
|
FA complementation group I
|
|
8.9E-37 |
0.543 |
0.731 |
| FANCD2 |
Q9BXW9
|
FA complementation group D2
|
|
1.1E-30 |
0.479 |
0.885 |
| BRCA1 |
P38398
|
BRCA1 DNA repair associated
|
Enzyme
|
9.2E-29 |
0.367 |
0.923 |
| NME8 |
Q8N427
|
NME/NM23 family member 8
|
|
5.6E-28 |
0.644 |
0.692 |
| CC2D2A |
Q9P2K1
|
coiled-coil and C2 domain containing 2A
|
|
1.7E-27 |
0.532 |
0.692 |
| CENPJ |
Q9HC77
|
centromere protein J
|
Enzyme
|
2.1E-27 |
0.546 |
0.846 |
| CEP152 |
O94986
|
centrosomal protein 152
|
Signaling
|
2.7E-27 |
0.653 |
0.500 |
| DNAH1 |
Q9P2D7
|
dynein axonemal heavy chain 1
|
Enzyme
|
1.5E-26 |
0.656 |
0.615 |
| ARMC4 |
Q5T2S8
|
armadillo repeat containing 4
|
|
1.9E-25 |
0.641 |
0.615 |
| BRCA2 |
P51587
|
BRCA2 DNA repair associated
|
Nucleic acid binding
|
2.4E-25 |
0.379 |
0.846 |
| HYDIN |
Q4G0P3
|
HYDIN axonemal central pair apparatus protein
|
|
2.3E-24 |
0.641 |
0.538 |