| Gene |
Chromosome |
Location |
Syndrome |
| AP4B1 | 1 | p13.2 | Cerebral palsy spastic quadriplegic type 5 (CPSQ5) disorder | |
| AP4E1 | 15 | q21.2 | Cerebral palsy spastic quadriplegic type 4 (CPSQ4) disorder | |
| AP4M1 | 7 | q22.1 | Cerebral palsy spastic quadriplegic type 3 (CPSQ3) disorder | |
| AP4S1 | 14 | q12 | Cerebral palsy spastic quadriplegic type 6 (CPSQ6) disorder | |
| DMD | 23 | p21.1 | Cerebral palsy - unassigned | |
| FA2H | 16 | q23 | Fatty acid hydroxylase-associated neurodegeneration (FAHN) | |
| GAD1 | 2 | q31 | Cerebral palsy spastic quadriplegic type 1 (CPSQ1) disorder | |
| GSN | 9 | q33 | Lattice corneal dystrophy type II | |
| HPSE2 | 10 | q23-24 | Ochoa syndrome | |
| HSPA4 | 5 | q31.1 | Cerebral palsy - unassigned | |
| KANK1 | 9 | p24.3 | Cerebral palsy spastic quadriplegic type 2 (CPSQ2) disorder | |
| MAPT | 17 | q21.1 | Progressive supranuclear palsy | |
| PACRG | 6 | q26 | Cerebral palsy - unassigned | |
| PMP22 | 17 | p12 | Hereditary neuropathy with liability to pressure palsies | |
| RAPGEF1 | 9 | q34.13 | Cerebral palsy - unassigned | |
| ROBO3 | 11 | q24.2 | Horizontal gaze palsy with progressive scoliosis (HGPPS) | |
| SLC12A6 | 15 | q13 | Andermann syndrome | |
| SLC52A3 | 20 | p13 | Brown-Vialetto-Van Laere syndrome (BVVLS) | |
| WNT4 | 1 | p36.12 | Cerebral palsy - unassigned | |