221
|
|
|
Meiosis specific with OB-fold |
C16orf73, POF23, SPGF22, gs129 |
|
222
|
|
|
MORN repeat containing 5 |
C9orf113, C9orf18 |
|
223
|
|
|
Major facilitator superfamily domain containing 8 |
CCMD, CLN7, SLC74A1 |
Cerebellar atrophy, Cerebral atrophy, Developmental delay, Disorder of eye, Dyssomnia, Age-related macular degeneration, Macular dystrophy with central cone involvement, Myoclonic seizures, Neuronal ceroid lipofuscinosis, Optic atrophy, Retinal diseases, Retinitis pigmentosa, Sleep disorders |
224
|
|
|
MAP7 domain containing 2 |
- |
|
225
|
|
|
Mitochondrial tRNA translation optimization 1 |
CGI-02, COXPD10 |
|
226
|
|
|
MOB family member 4, phocein |
2C4D, CGI-95, MOB1, MOB3, MOBKL3, PHOCN, PREI3 |
|
227
|
|
|
Mitochondrial pyruvate carrier 2 |
BRP44, SLC54A2 |
|
228
|
|
|
Matrix remodeling associated 5 |
- |
|
229
|
|
|
Methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1 like |
FTHFSDC1, MTC1THFS, dJ292B18.2 |
|
230
|
|
|
Myelodysplastic syndrome 2 translocation associated |
- |
|