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
ALPL	gene	ALPL	Expert Review Red;Literature	Tremors_Superpanel		Neurology and neurodevelopmental disorders	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	Hypophosphatasia, adult, MIM# 146300;Osteomalacia;Parkinsonism				PMID: 32956941		False	1	50;0;50	3.65	True		ENSG00000162551	ENSG00000162551	HGNC:438													
ANG	gene	ANG	Expert Review Red;Literature	Tremors_Superpanel		Neurology and neurodevelopmental disorders	Unknown	Parkinson disease MONDO:0005180				33875291;25386690		False	1	0;0;100	3.65	True		ENSG00000214274	ENSG00000214274	HGNC:483													
CACNA1B	gene	CACNA1B	Expert Review Red;Other	Tremors_Superpanel		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Myoclonus-dystonia syndrome MONDO:0000903				25296916;26157024;35698023;33051750;35041927		False	1	0;0;100	3.65	True		ENSG00000148408	ENSG00000148408	HGNC:1389													
CHMP2B	gene	CHMP2B	Expert Review Red;Royal Melbourne Hospital	Tremors_Superpanel		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	familial frontotemporal lobar degeneration (ALS17);Frontotemporal dementia and/or amyotrophic lateral sclerosis 1;Dystonia				20301378		False	1	0;0;100	3.65	True		ENSG00000083937	ENSG00000083937	HGNC:24537													
DCAF17	gene	DCAF17	Expert Review Red;Melbourne Genomics Health Alliance Complex Neurology Flagship;Victorian Clinical Genetics Services	Tremors_Superpanel		Neurology and neurodevelopmental disorders	Unknown							False	1	0;0;100	3.65	True		ENSG00000115827	ENSG00000115827	HGNC:25784													
DCTN1	gene	DCTN1	Expert Review Red;Expert list	Tremors_Superpanel		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Perry syndrome MIM#168605				24343258		False	1	0;0;100	3.65	True		ENSG00000204843	ENSG00000204843	HGNC:2711													
DNAJC13	gene	DNAJC13	Expert Review Red;Expert list	Tremors_Superpanel		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted					30788857;24218364;29309590;31082451;29887357;27270108		False	1	0;100;0	3.65	True		ENSG00000138246	ENSG00000138246	HGNC:30343													
DRD2	gene	DRD2	Expert Review Red;Literature	Tremors_Superpanel		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Combined dystonia, MONDO:0020065, DRD2-related;dystonia;chorea;anxiety;ataxia;orofacial dyskinesia;tremor;memory problems				33200438		False	1	100;0;0	3.65	True	Other	ENSG00000149295	ENSG00000149295	HGNC:3023													
EARS2	gene	EARS2	Expert Review Red;Expert list	Tremors_Superpanel		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Combined oxidative phosphorylation deficiency 12 MIM#614924				22492562		False	1	0;0;100	3.65	True		ENSG00000103356	ENSG00000103356	HGNC:29419													
FUS	gene	FUS	Expert Review Red;Literature	Tremors_Superpanel		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"tremor, hereditary essential, 4	MONDO:0013888"				22863194;23834483;23825177;38626532		False	1	0;0;100	3.65	True		ENSG00000089280	ENSG00000089280	HGNC:4010													
GIGYF2	gene	GIGYF2	Expert Review Red;Literature	Tremors_Superpanel		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	{Parkinson disease 11} , OMIM # 607688				18358451;33239198;25279164;20060621;19250854;26152800;19449032		False	1	0;50;50	3.65	True		ENSG00000204120	ENSG00000204120	HGNC:11960													
HEXA	gene	HEXA	Expert Review Red;Literature	Tremors_Superpanel		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	GM2 Gangliosidosis;Tay-Sachs disease;Parkinsonism;OMIM 272800				PMID: 33069254		False	1	50;0;50	3.65	True		ENSG00000213614	ENSG00000213614	HGNC:4878													
MAT1A	gene	MAT1A	Expert Review Red;Expert list	Tremors_Superpanel		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Methionine adenosyltransferase deficiency, autosomal recessive MIM#250850				8770875		False	1	0;0;100	3.65	True		ENSG00000151224	ENSG00000151224	HGNC:6903													
MMADHC	gene	MMADHC	Expert Review Red;Expert list	Tremors_Superpanel		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Homocystinuria, cblD type, variant 1 MIM#277410				15292234;18385497		False	1	0;0;100	3.65	True		ENSG00000168288	ENSG00000168288	HGNC:25221													
MOGS	gene	MOGS	Expert Review Red;Expert Review	Tremors_Superpanel		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Congenital disorder of glycosylation, type IIb, MIM# 606056				33058492		False	1	0;0;100	3.65	True		ENSG00000115275	ENSG00000115275	HGNC:24862													
MPV17	gene	MPV17	Expert Review Red;Expert list	Tremors_Superpanel		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type) MIM#256810				29282788		False	1	0;0;100	3.65	True		ENSG00000115204	ENSG00000115204	HGNC:7224													
OPA3	gene	OPA3	Expert Review Red;Melbourne Genomics Health Alliance Complex Neurology Flagship;Victorian Clinical Genetics Services	Tremors_Superpanel		Neurology and neurodevelopmental disorders	Unknown							False	1	0;0;100	3.65	True		ENSG00000125741	ENSG00000125741	HGNC:8142													
PDGFRB	gene	PDGFRB	Expert Review Red;Royal Melbourne Hospital	Tremors_Superpanel		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Basal ganglia calcification, idiopathic, 4, MIM# 615007				24518837		False	1	0;0;100	3.65	True		ENSG00000113721	ENSG00000113721	HGNC:8804													
PLP1	gene	PLP1	Expert Review Red;Expert list	Tremors_Superpanel		Neurology and neurodevelopmental disorders	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Pelizaeus-Merzbacher disease MIM#312080				30046645;19396823		False	1	0;0;100	3.65	True		ENSG00000123560	ENSG00000123560	HGNC:9086													
PODXL	gene	PODXL	Expert Review Red;Expert list	Tremors_Superpanel		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	juvenile-onset Parkinson disease				26864383		False	1	0;0;100	3.65	True		ENSG00000128567	ENSG00000128567	HGNC:9171													
PODXL	gene	PODXL	Literature	Tremors_Superpanel		Neurology and neurodevelopmental disorders	Unknown	juvenile-onset Parkinson disease				26864383;20706633		False	1	0;100;0	3.65	False		ENSG00000128567	ENSG00000128567	HGNC:9171													
PSEN2	gene	PSEN2	Expert Review Red;Other	Tremors_Superpanel		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Parkinsonism;Alzheimer disease-4 MIM#606889				22118943;26422362;18427071;29692703		False	1	0;0;100	3.65	True		ENSG00000143801	ENSG00000143801	HGNC:9509													
RELN	gene	RELN	Expert Review Red;Other	Tremors_Superpanel		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Myoclonus-dystonia syndrome MONDO:0000903				32334381;25648840		False	1	0;0;100	3.65	True		ENSG00000189056	ENSG00000189056	HGNC:9957													
RIC3	gene	RIC3	Expert Review Red;Other	Tremors_Superpanel		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Parkinson disease				27055476;28153381;28606768;32794657		False	1	0;0;100	3.65	True		ENSG00000166405	ENSG00000166405	HGNC:30338													
RNASEH2A	gene	RNASEH2A	Expert Review Red;Expert list	Tremors_Superpanel		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Aicardi-Goutieres syndrome 4 MIM#610333				20131292		False	1	0;0;100	3.65	True		ENSG00000104889	ENSG00000104889	HGNC:18518													
SLC20A2	gene	SLC20A2	Expert Review Red;Expert list	Tremors_Superpanel		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Basal ganglia calcification, idiopathic, 1, MIM# 213600;Paroxysmal kinesigenic dyskinesia				22327515;23334463;24411498		False	1	0;0;100	3.65	True		ENSG00000168575	ENSG00000168575	HGNC:10947													
TMEM230	gene	TMEM230	Expert list	Tremors_Superpanel		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Parkinson disease 21, MIM#616361				30804554;27270108;28115417;28017548;30804555;30804556;31323517		False	1	0;100;0	3.65	False		ENSG00000089063	ENSG00000089063	HGNC:15876													
TOR1AIP1	gene	TOR1AIP1	Expert Review Red;Royal Melbourne Hospital	Tremors_Superpanel		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Dystonia, cerebellar atrophy, and cardiomyopathy				25425325		False	1	0;0;100	3.65	True		ENSG00000143337	ENSG00000143337	HGNC:29456													
TUBB4A	gene	TUBB4A	Expert Review Red;Melbourne Genomics Health Alliance Complex Neurology Flagship;Victorian Clinical Genetics Services	Tremors_Superpanel		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted							False	1	0;0;100	3.65	True		ENSG00000104833	ENSG00000104833	HGNC:20774													
UBR4	gene	UBR4	Expert Review Red;Expert list	Tremors_Superpanel		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	early onset episodic ataxia;nystagmus;myokymia;tremor				23982692;29062094		False	1	0;0;100	3.65	True		ENSG00000127481	ENSG00000127481	HGNC:30313													
UNC80	gene	UNC80	Expert Review Red;Expert list	Tremors_Superpanel		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Hypotonia, infantile, with psychomotor retardation and characteristic facies 2, MIM# 616801;MONDO:0014777				26545877		False	1	0;0;100	3.65	True		ENSG00000144406	ENSG00000144406	HGNC:26582													
VPS11	gene	VPS11	Expert Review Red;Literature	Tremors_Superpanel		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Dystonia 32, MIM# 619637;Dystonia, adult-onset				33452836		False	1	0;0;100	3.65	True		ENSG00000160695	ENSG00000160695	HGNC:14583													
VPS37A	gene	VPS37A	Expert Review Red;Expert list	Tremors_Superpanel		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Spastic paraplegia 53, autosomal recessive MIM#614898				22717650		False	1	0;0;100	3.65	True		ENSG00000155975	ENSG00000155975	HGNC:24928													
WASL	gene	WASL	Expert Review Red;Literature	Tremors_Superpanel		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Parkinson's disease, MONDO:0005180, WASL-related				PMID: 33571872		False	1	50;0;50	3.65	True		ENSG00000106299	ENSG00000106299	HGNC:12735