| HTC2 |
|
hypertrichosis 2 (generalized, congenital)
|
|
|
0.392 |
0.808 |
| MIR122 |
|
microRNA 122
|
|
|
0.468 |
0.808 |
| PWAR1 |
|
Prader Willi/Angelman region RNA 1
|
|
|
0.490 |
0.769 |
| MIR23A |
|
microRNA 23a
|
|
|
0.499 |
0.808 |
| CYTB |
P00156
|
cytochrome b
|
|
|
0.529 |
0.808 |
| BTF3P11 |
|
basic transcription factor 3 pseudogene 11
|
|
|
0.519 |
0.731 |
| THAS |
|
thoracoabdominal syndrome
|
|
|
0.560 |
0.808 |
| ANKRD36B |
Q8N2N9
|
ankyrin repeat domain 36B
|
|
|
0.584 |
0.500 |
| 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 |
| FRAXA |
|
fragile site, folic acid type, rare, fra(X)(q27.3) A (macroorchidism, mental retardation)
|
|
|
0.641 |
0.462 |
| SNHG14 |
|
small nucleolar RNA host gene 14
|
|
|
0.656 |
0.577 |
| SNORD15A |
|
small nucleolar RNA, C/D box 15A
|
|
|
0.653 |
0.577 |
| SNORD35B |
|
small nucleolar RNA, C/D box 35B
|
|
|
0.653 |
0.538 |
| SNORD14C |
|
small nucleolar RNA, C/D box 14C
|
|
|
0.653 |
0.538 |
| SNORD14D |
|
small nucleolar RNA, C/D box 14D
|
|
|
0.653 |
0.538 |
| SNORD14E |
|
small nucleolar RNA, C/D box 14E
|
|
|
0.653 |
0.538 |
| SNORD14B |
|
small nucleolar RNA, C/D box 14B
|
|
|
0.656 |
0.538 |
| SNORD116@ |
|
small nucleolar RNA, C/D box 116 cluster
|
|
|
0.705 |
0.692 |
| FMR1-IT1 |
|
FMR1 intronic transcript 1
|
|
|
0.716 |
0.385 |
| DAZ1 |
Q9NQZ3
|
deleted in azoospermia 1
|
Nucleic acid binding
|
|
0.705 |
0.385 |