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
TUBA1A	gene	TUBA1A	Australian Genomics Health Alliance Brain Malformations Flagship;Expert Review Green;Victorian Clinical Genetics Services	Tubulinopathies		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted				Abnormal cortical gyration;HP:0002536			False	3	100;0;0	1.2	False		ENSG00000167552	ENSG00000167552	HGNC:20766													
TUBB	gene	TUBB	Australian Genomics Health Alliance Brain Malformations Flagship;Expert Review Green;Victorian Clinical Genetics Services	Tubulinopathies		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Cortical dysplasia, complex, with other brain malformations 6, MIM# 615771			Abnormal cortical gyration;HP:0002536	23246003;32085672		False	3	100;0;0	1.2	True		ENSG00000196230	ENSG00000196230	HGNC:20778													
TUBB2A	gene	TUBB2A	Australian Genomics Health Alliance Brain Malformations Flagship;Expert Review Green;Victorian Clinical Genetics Services	Tubulinopathies		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Cortical dysplasia, complex, with other brain malformations 5, MIM# 615763			Abnormal cortical gyration;HP:0002536	32571897		False	3	100;0;0	1.2	True		ENSG00000137267	ENSG00000137267	HGNC:12412													
TUBB2B	gene	TUBB2B	Australian Genomics Health Alliance Brain Malformations Flagship;Expert Review Green;Victorian Clinical Genetics Services	Tubulinopathies		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Cortical dysplasia, complex, with other brain malformations 7, MIM# 610031			Abnormal cortical gyration;HP:0002536	19465910;22333901;26732629;33082561		False	3	100;0;0	1.2	True		ENSG00000137285	ENSG00000137285	HGNC:30829													
TUBB3	gene	TUBB3	Australian Genomics Health Alliance Brain Malformations Flagship;Expert Review Green;Victorian Clinical Genetics Services	Tubulinopathies		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Cortical dysplasia, complex, with other brain malformations 1, MIM# 614039			Abnormal cortical gyration;HP:0002536	20829227;25059107;33318778		False	3	100;0;0	1.2	True		ENSG00000258947	ENSG00000258947	HGNC:20772													
TUBG1	gene	TUBG1	Australian Genomics Health Alliance Brain Malformations Flagship;Expert Review Green;Victorian Clinical Genetics Services	Tubulinopathies		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Cortical dysplasia, complex, with other brain malformations 4, MIM# 615412			Abnormal cortical gyration;HP:0002536	23603762;31086189		False	3	100;0;0	1.2	True		ENSG00000131462	ENSG00000131462	HGNC:12417