| HTC2 |
|
hypertrichosis 2 (generalized, congenital)
|
|
|
0.392 |
0.808 |
| MIR143 |
|
microRNA 143
|
|
|
0.462 |
0.885 |
| MAA |
|
microphthalmia or anophthalmia and associated anomalies
|
|
|
0.666 |
0.577 |
| TRP-AGG2-6 |
|
tRNA-Pro (anticodon AGG) 2-6
|
|
|
0.666 |
0.462 |
| MIR508 |
|
microRNA 508
|
|
|
0.705 |
0.385 |
| AIC |
|
Aicardi syndrome
|
|
|
0.729 |
0.462 |
| TRP-AGG2-5 |
|
tRNA-Pro (anticodon AGG) 2-5
|
|
|
0.722 |
0.423 |
| MCOPCT1 |
|
cataract, congenital, with microphthalmia
|
|
|
0.931 |
0.077 |
| NNO1 |
|
nanophthalmos 1
|
|
|
1.000 |
0.077 |
| MCOP1 |
|
microphthalmia, autosomal recessive
|
|
|
1.000 |
0.077 |
| FANCA |
O15360
|
FA complementation group A
|
|
1.6E-68 |
0.505 |
0.731 |
| CEP290 |
O15078
|
centrosomal protein 290
|
|
1.1E-60 |
0.517 |
0.769 |
| FREM1 |
Q5H8C1
|
FRAS1 related extracellular matrix 1
|
|
1.6E-52 |
0.633 |
0.423 |
| VPS13B |
Q7Z7G8
|
vacuolar protein sorting 13 homolog B
|
|
2.5E-45 |
0.579 |
0.769 |
| FRAS1 |
Q86XX4
|
Fraser extracellular matrix complex subunit 1
|
|
3.1E-45 |
0.560 |
0.577 |
| TRPM1 |
Q7Z4N2
|
transient receptor potential cation channel subfamily M member 1
|
Ion channel
|
1.6E-42 |
0.626 |
0.462 |
| FANCI |
Q9NVI1
|
FA complementation group I
|
|
8.9E-37 |
0.543 |
0.731 |
| CENPF |
P49454
|
centromere protein F
|
|
1.9E-36 |
0.601 |
0.654 |
| RECQL4 |
O94761
|
RecQ like helicase 4
|
Enzyme
|
3.3E-35 |
0.496 |
0.808 |
| TYR |
P14679
|
tyrosinase
|
Enzyme
|
5.0E-32 |
0.473 |
0.808 |
| TUBGCP6 |
Q96RT7
|
tubulin gamma complex associated protein 6
|
Cellular structure
|
2.6E-31 |
0.695 |
0.308 |
| RPGRIP1L |
Q68CZ1
|
RPGRIP1 like
|
Enzyme modulator
|
4.1E-31 |
0.534 |
0.769 |
| FANCD2 |
Q9BXW9
|
FA complementation group D2
|
|
1.1E-30 |
0.479 |
0.885 |
| CNKSR1 |
Q969H4
|
connector enhancer of kinase suppressor of Ras 1
|
|
4.3E-30 |
0.769 |
0.462 |
| CSPP1 |
Q1MSJ5
|
centrosome and spindle pole associated protein 1
|
|
3.3E-29 |
0.544 |
0.769 |