| HTC2 |
|
hypertrichosis 2 (generalized, congenital)
|
|
|
0.392 |
0.808 |
| MIR10B |
|
microRNA 10b
|
|
|
0.509 |
0.808 |
| MIR10A |
|
microRNA 10a
|
|
|
0.513 |
0.846 |
| BTF3P11 |
|
basic transcription factor 3 pseudogene 11
|
|
|
0.519 |
0.731 |
| MIR320A |
|
microRNA 320a
|
|
|
0.526 |
0.808 |
| THAS |
|
thoracoabdominal syndrome
|
|
|
0.560 |
0.808 |
| CECR |
|
cat eye syndrome chromosome region
|
|
|
0.599 |
0.731 |
| HYMAI |
|
hydatidiform mole associated and imprinted
|
|
|
0.670 |
0.538 |
| DGCR |
|
DiGeorge syndrome chromosome region
|
|
|
0.678 |
0.538 |
| AOS |
|
Adams-Oliver syndrome
|
|
|
0.792 |
0.462 |
| STX18-AS1 |
|
STX18 antisense RNA 1 (head to head)
|
|
|
0.890 |
0.154 |
| RRDX |
|
Radial ray deficiency
|
|
|
0.805 |
0.154 |
| SHFM5 |
|
split hand/foot malformation (ectrodactyly) type 5
|
|
|
0.839 |
0.115 |
| NANOGP1 |
Q8N7R0
|
Nanog homeobox pseudogene 1
|
|
|
0.931 |
0.269 |
| MIB1 |
Q86YT6
|
mindbomb E3 ubiquitin protein ligase 1
|
Enzyme
|
3.4E-88 |
0.438 |
0.769 |
| FANCA |
O15360
|
FA complementation group A
|
|
1.6E-68 |
0.505 |
0.731 |
| DNAH8 |
Q96JB1
|
dynein axonemal heavy chain 8
|
Enzyme
|
1.1E-60 |
0.556 |
0.731 |
| PKHD1 |
P08F94
|
PKHD1 ciliary IPT domain containing fibrocystin/polyductin
|
|
1.2E-47 |
0.576 |
0.654 |
| FRAS1 |
Q86XX4
|
Fraser extracellular matrix complex subunit 1
|
|
3.1E-45 |
0.560 |
0.577 |
| PKD1L1 |
Q8TDX9
|
polycystin 1 like 1, transient receptor potential channel interacting
|
Ion channel
|
1.1E-40 |
0.729 |
0.231 |
| DNMT3A |
Q9Y6K1
|
DNA methyltransferase 3 alpha
|
|
7.4E-39 |
0.445 |
0.846 |
| ACE |
P12821
|
angiotensin I converting enzyme
|
Enzyme
|
1.0E-37 |
0.328 |
0.923 |
| CPLANE1 |
Q9H799
|
ciliogenesis and planar polarity effector 1
|
|
5.9E-36 |
0.575 |
0.692 |
| RECQL4 |
O94761
|
RecQ like helicase 4
|
Enzyme
|
3.3E-35 |
0.496 |
0.808 |
| DYSF |
O75923
|
dysferlin
|
Transporter
|
3.7E-33 |
0.582 |
0.692 |