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GTD Indications Diagnosis Prenatal GTD Samples Accepted Blood DNA GTD Test Methodology CNV Sequencing GTD Methodology Notes Exome + targeted microarray Generic Test name (cms title) Hereditary Spastic Paraplegia GTD Test type Gene Panel GTD Location The Hospital for Sick Children GTD Gene/Platform/Region List ABCD1, ADAR, ALDH18A1, ALS2, AP4B1, AP4E1, AP4M1, AP4S1, AP5Z1, ATL1, ATP13A2, B4GALNT1, BSCL2, C19orf12, CAPN1, CPT1C, CYP2U1, CYP7B1, DDHD1, DDHD2, ERLIN1, ERLIN2, FA2H, FAR1, FARS2, GBA2, HACE1, HPDL, HSPD1, IBA57, IFIH1, KIDINS220, KIF1A, KIF1C, KIF5A, L1CAM, MAG, MTRFR, NIPA1, NT5C2, PCYT2, PLP1, PNPLA6, POLG, POLR3A, POLR3B, REEP1, REEP2, RNF170, RTN2, SACS, SELENOI, SETX, SLC16A2, SPART, SPAST, SPG11, SPG21, SPG7, TECPR2, TFG, TUBB4A, UBAP1, UCHL1, VPS13D, WASHC5, ZFYVE26 GTD Category Neurogenetics GTD Disease/Condition Hereditary Spastic Paraplegia