Entity Name	Entity type	Gene Symbol	Sources(; separated)	Level4	Level3	Level2	Model_Of_Inheritance	Phenotypes	Omim	Orphanet	HPO	Publications	Description	Flagged	GEL_Status	UserRatings_Green_amber_red	version	ready	Mode of pathogenicity	EnsemblId(GRch37)	EnsemblId(GRch38)	HGNC	Position Chromosome	Position GRCh37 Start	Position GRCh37 End	Position GRCh38 Start	Position GRCh38 End	STR Repeated Sequence	STR Normal Repeats	STR Pathogenic Repeats	Region Haploinsufficiency Score	Region Triplosensitivity Score	Region Required Overlap Percentage	Region Variant Type	Region Verbose Name
COQ7	gene	COQ7	Literature	Hereditary Spastic Paraplegia - adult onset		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Hereditary spastic paraplegia, COQ7-related (MONDO#0019064)			Spasticity;HP:0001257	PMID: 33215859		False	1	0;0;100	1.19	False		ENSG00000167186	ENSG00000167186	HGNC:2244													
DNM2	gene	DNM2	Expert Review Red;Royal Melbourne Hospital	Hereditary Spastic Paraplegia - adult onset		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Complicated hereditary spastic paraplegia			Spasticity;HP:0001257	26517984		False	1	0;0;100	1.19	True		ENSG00000079805	ENSG00000079805	HGNC:2974													
SLC33A1	gene	SLC33A1	Expert list;Expert Review Red;Royal Melbourne Hospital	Hereditary Spastic Paraplegia - adult onset		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Spastic paraplegia 42, autosomal dominant;Congenital cataracts, hearing loss, and neurodegeneration 614482, AR:Spastic paraplegia 42, autosomal dominant, 612539 AD			Spasticity;HP:0001257	27935820;19061983		False	1	0;0;100	1.19	True		ENSG00000169359	ENSG00000169359	HGNC:95													
TSPOAP1	gene	TSPOAP1	Expert Review Red;Literature	Hereditary Spastic Paraplegia - adult onset		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Dystonia 22, MIM# 620453			Spasticity;HP:0001257	33539324		False	1	0;50;50	1.19	True		ENSG00000005379	ENSG00000005379	HGNC:16831													
ZFYVE27	gene	ZFYVE27	Expert Review Red;Royal Melbourne Hospital	Hereditary Spastic Paraplegia - adult onset		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Spastic paraplegia 33, autosomal dominant, MIM#610244			Spasticity;HP:0001257	29980238;18606302;16826525		False	1	0;0;100	1.19	True		ENSG00000155256	ENSG00000155256	HGNC:26559