Test 54.
Hereditary spastic paraplegia
Mutations in 111 genes associated with hereditary spastic paraplegia
ABCD1, ABHD16A, ADAR, AFG3L2, AIMP1, ALDH18A1, ALS2, AMPD2, AP4B1, AP4E1, AP4M1, AP4S1, AP5Z1, ARG1, ARL6IP1, ARSI, ATAD3A, ATL1, ATP13A2, B4GALNT1, BICD2, BSCL2, C12orf65, C19orf12, CAPN1, CCT5, CDK16, CPT1C, CTNNB1, CYP27A1, CYP2U1, CYP7B1, DARS1, DDHD1, DDHD2, DSTYK, ENTPD1, EPT1, ERLIN1, ERLIN2, EXOSC3, FA2H, FARS2, GAD1, GBA2, GCH1, GJC2, HACE1, HIKESHI, HSPD1, IBA57, IFIH1, INTS8, IRF2BPL, KDM5C, KIDINS220, KIF1A, KIF1C, KIF5A, KLC2, KLC4, KY, L1CAM, MAG, MARS2, MTPAP, NIPA1, NKX6-2, NT5C2, OPA3, PCDH12, PCYT2, PGAP1, PLP1, PNPLA6, POLR3A, POLR3K, PSEN1, RAB3GAP2, REEP1, REEP2, RNASEH2B, RTN2, SACS, SARS2, SERAC1, SHMT2, SLC16A2, SLC1A4, SLC25A46, SLC2A1, SLC33A1, SPART, SPAST, SPG11, SPG21, SPG7, TECPR2, TFG, TOE1, TUBB4A, UBAP1, UCHL1, VAMP1, VPS37A, WASHC5, WDR45B, WDR48, ZEB2, ZFYVE26, ZFYVE27