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
CACNA1H	gene	CACNA1H	Expert Review Red;Victorian Clinical Genetics Services	Autism		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Autism spectrum disorder			Autism;HP:0000717	16754686;32571372		False	1	0;0;100	0.205	True		ENSG00000196557	ENSG00000196557	HGNC:1395													
CACNA2D3	gene	CACNA2D3	Expert Review Red;Victorian Clinical Genetics Services	Autism		Neurology and neurodevelopmental disorders	Unknown				Autism;HP:0000717	31275518;22542183;23375656		False	1	0;0;100	0.205	True		ENSG00000157445	ENSG00000157445	HGNC:15460													
CNTN4	gene	CNTN4	Expert Review Red;Victorian Clinical Genetics Services	Autism		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Intellectual disability;SCA			Autism;HP:0000717	15106122;18349135;17932120		False	1	0;0;100	0.205	True		ENSG00000144619	ENSG00000144619	HGNC:2174													
GIGYF2	gene	GIGYF2	Expert Review Red;Victorian Clinical Genetics Services	Autism		Neurology and neurodevelopmental disorders	Unknown				Autism;HP:0000717			False	1	0;0;100	0.205	False		ENSG00000204120	ENSG00000204120	HGNC:11960													
HDAC4	gene	HDAC4	Expert Review Red;Victorian Clinical Genetics Services	Autism		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Brachydactyly mental retardation syndrome;Brachydactyly without intellectual disability			Autism;HP:0000717	24715439;20691407;31209962		False	1	0;0;100	0.205	True		ENSG00000068024	ENSG00000068024	HGNC:14063													
ILF2	gene	ILF2	Expert Review Red;Victorian Clinical Genetics Services	Autism		Neurology and neurodevelopmental disorders	Unknown	Autism			Autism;HP:0000717	26402605		False	1	0;0;100	0.205	True		ENSG00000143621	ENSG00000143621	HGNC:6037													
INTS6	gene	INTS6	Expert Review Red;Victorian Clinical Genetics Services	Autism		Neurology and neurodevelopmental disorders	Unknown				Autism;HP:0000717			False	1	0;0;100	0.205	True		ENSG00000102786	ENSG00000102786	HGNC:14879													
MET	gene	MET	Expert list;Expert Review Red;Victorian Clinical Genetics Services	Autism		Neurology and neurodevelopmental disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	?Deafness, autosomal recessive 97, OMIM #616705;{Osteofibrous dysplasia, susceptibility to}, OMIM #607278			Autism;HP:0000717			False	1	0;0;100	0.205	True		ENSG00000105976	ENSG00000105976	HGNC:7029													
NTNG1	gene	NTNG1	Expert Review Red;Victorian Clinical Genetics Services	Autism		Neurology and neurodevelopmental disorders	Unknown				Autism;HP:0000717			False	1	0;0;100	0.205	True		ENSG00000162631	ENSG00000162631	HGNC:23319													
RANBP17	gene	RANBP17	Expert Review Red;Victorian Clinical Genetics Services	Autism		Neurology and neurodevelopmental disorders	Unknown				Autism;HP:0000717			False	1	0;0;100	0.205	True		ENSG00000204764	ENSG00000204764	HGNC:14428													
RELN	gene	RELN	Expert Review Red;Victorian Clinical Genetics Services	Autism		Neurology and neurodevelopmental disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Lissencephaly 2 (Norman-Roberts type), MIM# 257320;ASD			Autism;HP:0000717	28419454;29969175		False	1	50;0;50	0.205	True		ENSG00000189056	ENSG00000189056	HGNC:9957													
RNF135	gene	RNF135	Expert Review Red;Victorian Clinical Genetics Services	Autism		Neurology and neurodevelopmental disorders	Unknown				Autism;HP:0000717			False	1	0;0;100	0.205	True		ENSG00000181481	ENSG00000181481	HGNC:21158													
SLC9A9	gene	SLC9A9	Expert list;Expert Review Red	Autism		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	{?Autism susceptibility 16}, MIM# 613410			Autism;HP:0000717	18621663;31134136;27123481;26755066		False	1	0;0;100	0.205	True		ENSG00000181804	ENSG00000181804	HGNC:20653													
SYNE1	gene	SYNE1	Expert Review Red;Victorian Clinical Genetics Services	Autism		Neurology and neurodevelopmental disorders	Unknown				Autism;HP:0000717			False	1	0;0;100	0.205	True		ENSG00000131018	ENSG00000131018	HGNC:17089													
TMLHE	gene	TMLHE	Expert list;Expert Review Red	Autism		Neurology and neurodevelopmental disorders	X-LINKED: hemizygous mutation in males, biallelic mutations in females	{Autism, susceptibility to, X-linked 6}, MIM#300872			Autism;HP:0000717	21865298		False	1	100;0;0	0.205	False		ENSG00000185973	ENSG00000185973	HGNC:18308													
TMPRSS9	gene	TMPRSS9	Expert Review Red;Literature	Autism		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	autism spectrum disorder			Autism;HP:0000717	31943016		False	1	0;0;100	0.205	True		ENSG00000178297	ENSG00000178297	HGNC:30079													
UNC13A	gene	UNC13A	Expert Review Red;Victorian Clinical Genetics Services	Autism		Neurology and neurodevelopmental disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Congenital myasthenia;dyskinesia;autism;developmental delay			Autism;HP:0000717	27648472;28192369		False	1	0;0;100	0.205	True		ENSG00000130477	ENSG00000130477	HGNC:23150