| H3P10 |
|
H3 histone pseudogene 10
|
|
|
0.350 |
0.846 |
| HTC2 |
|
hypertrichosis 2 (generalized, congenital)
|
|
|
0.392 |
0.808 |
| MEG3 |
|
maternally expressed 3
|
|
|
0.471 |
0.846 |
| RNU4ATAC |
|
RNA, U4atac small nuclear (U12-dependent splicing)
|
|
|
0.556 |
0.808 |
| H3P9 |
|
H3 histone pseudogene 9
|
|
|
0.505 |
0.731 |
| TMX2-CTNND1 |
|
TMX2-CTNND1 readthrough (NMD candidate)
|
|
|
0.538 |
0.769 |
| ATHS |
|
atherosclerosis susceptibility (lipoprotein associated)
|
|
|
0.551 |
0.769 |
| NPHP3-ACAD11 |
|
NPHP3-ACAD11 readthrough (NMD candidate)
|
|
|
0.663 |
0.577 |
| H3P47 |
|
H3 histone pseudogene 47
|
|
|
0.603 |
0.538 |
| HFM |
|
Hemifacial microsomia
|
|
|
0.722 |
0.385 |
| SHFM3 |
|
Split-hand/foot malformation 3
|
|
|
0.780 |
0.115 |
| AFA |
|
ankyloblepharon filiforme adnatum
|
|
|
0.792 |
0.462 |
| ERVMER61-1 |
|
endogenous retrovirus group MER61 member 1
|
|
|
0.890 |
0.115 |
| OFC2 |
|
orofacial cleft 2
|
|
|
0.931 |
0.115 |
| SHFL1 |
|
Split-hand/foot malformation with long bone deficiency 1
|
|
|
1.000 |
0.038 |
| MACOM |
|
macrophthalmia, colobomatous, with microcornea
|
|
|
1.000 |
0.077 |
| SMCHD1 |
A6NHR9
|
structural maintenance of chromosomes flexible hinge domain containing 1
|
|
1.00 |
0.631 |
0.615 |
| KPNA7 |
A9QM74
|
karyopherin subunit alpha 7
|
|
3.4E-15 |
0.805 |
0.308 |
| PRNP |
F7VJQ1 P04156
|
prion protein
|
|
6.3E-04 |
0.445 |
0.923 |
| KIF2A |
O00139
|
kinesin family member 2A
|
Cellular structure
|
1.00 |
0.590 |
0.731 |
| BMPR1B |
O00238
|
bone morphogenetic protein receptor type 1B
|
Kinase
|
1.00 |
0.573 |
0.615 |
| PIK3CD |
O00329
|
phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta
|
Kinase
|
1.00 |
0.319 |
0.885 |
| EML1 |
O00423
|
EMAP like 1
|
|
1.00 |
0.705 |
0.462 |
| KRIT1 |
O00522
|
KRIT1 ankyrin repeat containing
|
|
6.9E-04 |
0.500 |
0.808 |
| WNT7A |
O00755
|
Wnt family member 7A
|
Signaling
|
3.6E-02 |
0.531 |
0.692 |