| Gene | Uniprot | Gene Full Name | Protein Class | pLI | DSI v | DPI v |
|---|---|---|---|---|---|---|
| SRY | Q05066 | sex determining region Y | Transcription factor | 0.456 | 0.808 | |
| MIR29A | microRNA 29a | 0.459 | 0.808 | |||
| NEFL | P07196 | neurofilament light | 0.488 | 0.769 | ||
| CBLL2 | Q8N7E2 | Cbl proto-oncogene like 2 | Enzyme | 0.476 | 0.808 | |
| ATP6 | P00846 | ATP synthase F0 subunit 6 | Transporter | 0.541 | 0.731 | |
| HPT | hypoparathyroidism | 0.593 | 0.692 | |||
| RAB7B | Q96AH8 | RAB7B, member RAS oncogene family | 0.615 | 0.731 | ||
| GBAP1 | glucosylceramidase beta pseudogene 1 | 0.623 | 0.538 | |||
| PRS | Prieto X-linked mental retardation syndrome | 0.663 | 0.615 | |||
| RIEG2 | Rieger syndrome 2 | 0.674 | 0.462 | |||
| GLC3B | glaucoma 3, primary infantile, B | 0.769 | 0.154 | |||
| GUSBP14 | GUSB pseudogene 14 | 0.839 | 0.077 | |||
| CMTX3 | Charcot-Marie-Tooth neuropathy, X-linked 3 (dominant) | 0.821 | 0.154 | |||
| DFNA7 | deafness, autosomal dominant 7 | 0.861 | 0.154 | |||
| DFNA49 | deafness, autosomal dominant 49 | 0.861 | 0.154 | |||
| GUSBP3 | GUSB pseudogene 3 | 0.861 | 0.077 | |||
| GUSBP1 | Q15486 | GUSB pseudogene 1 | 0.861 | 0.077 | ||
| MBS2 | Moebius syndrome 2 | 0.931 | 0.115 | |||
| D1S111 | Minisatellite 33.6 | 0.931 | 0.115 | |||
| CMTX2 | Charcot-Marie-Tooth neuropathy, X-linked 2 (recessive) | 1.000 | 0.077 | |||
| TTN | Q8WZ42 | titin | Kinase | 2.6E-96 | 0.470 | 0.885 |
| MYO15A | Q9UKN7 | myosin XVA | Cellular structure | 1.3E-56 | 0.722 | 0.346 |
| MYO1A | Q9UBC5 | myosin IA | Cellular structure | 8.9E-46 | 0.769 | 0.269 |
| SPG11 | Q96JI7 | SPG11 vesicle trafficking associated, spatacsin | 1.6E-39 | 0.576 | 0.538 | |
| ACE | P12821 | angiotensin I converting enzyme | Enzyme | 1.0E-37 | 0.328 | 0.923 |