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
DIP2C	gene	DIP2C	Expert list;Expert Review;Expert Review Amber	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Neurodevelopmental disorder (MONDO:0700092), DIP2C-related				36117209;38421105		False	2	0;100;0	1.27	True		ENSG00000151240	ENSG00000151240	HGNC:29150													
ERF	gene	ERF	Expert list;Expert Review;Expert Review Amber	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Craniosynostosis 4, MIM# 600775				36117209;35761471;35852485		False	2	0;0;100	1.27	True		ENSG00000105722	ENSG00000105722	HGNC:3444													
GNAO1	gene	GNAO1	Expert list;Expert Review;Expert Review Amber	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Developmental and epileptic encephalopathy 17, MIM# 615473;Neurodevelopmental disorder with involuntary movements, MIM# 617493				32345733;35722775;38881224		False	2	0;0;100	1.27	True		ENSG00000087258	ENSG00000087258	HGNC:4389													
MEIS2	gene	MEIS2	Expert list;Expert Review;Expert Review Amber	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Cleft palate, cardiac defects, and impaired intellectual development, MIM# 600987				32345733;30055086		False	2	0;100;0	1.27	True		ENSG00000134138	ENSG00000134138	HGNC:7001													
MKL2	gene	MKL2	Expert list;Expert Review;Expert Review Amber	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Neurodevelopmental disorder (MONDO:0700092), MKL2-related				29463886;37013900;38366112		False	2	0;50;50	1.27	True		ENSG00000186260	ENSG00000186260	HGNC:29819													
RBFOX3	gene	RBFOX3	Expert list;Expert Review;Expert Review Amber	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Neurodevelopmental disorder (MONDO:0700092), RBFOX3-related				36117209;24039908		False	2	0;100;0	1.27	True		ENSG00000167281	ENSG00000167281	HGNC:27097													
SHANK3	gene	SHANK3	Expert list;Expert Review;Expert Review Amber	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Phelan-McDermid syndrome, MIM# 606232				36117209;33293697		False	2	0;100;0	1.27	True		ENSG00000251322	ENSG00000251322	HGNC:14294													
TNRC6B	gene	TNRC6B	Expert list;Expert Review;Expert Review Amber	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Global developmental delay with speech and behavioral abnormalities, MIM# 619243				29463886;32152250;38300321;38404251		False	2	0;0;100	1.27	True		ENSG00000100354	ENSG00000100354	HGNC:29190													
WDR5	gene	WDR5	Expert list;Expert Review;Expert Review Amber	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Neurodevelopmental disorder (MONDO:0700092), WDR5-related				29463886;36408368		False	2	0;100;0	1.27	True		ENSG00000196363	ENSG00000196363	HGNC:12757													
ZNF142	gene	ZNF142	Expert list;Expert Review;Expert Review Amber	Speech apraxia		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Neurodevelopmental disorder with impaired speech and hyperkinetic movements, MIM# 618425				32345733;31036918;34531528;35616059		False	2	0;100;0	1.27	True		ENSG00000115568	ENSG00000115568	HGNC:12927