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
ANK2	gene	ANK2	Expert Review;Expert Review Red	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Neurodevelopmental disorder (MONDO:0700092), gene-related				37195288		False	1	0;0;100	1.27	True		ENSG00000145362	ENSG00000145362	HGNC:493													
ARHGEF9	gene	ARHGEF9	Expert list;Expert Review;Expert Review Red	Speech apraxia		Neurology and neurodevelopmental disorders	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Developmental and epileptic encephalopathy 8, MIM# 300607				36117209		False	1	0;0;100	1.27	True		ENSG00000131089	ENSG00000131089	HGNC:14561													
BPTF	gene	BPTF	Expert list;Expert Review;Expert Review Red	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies, MIM# 617755						False	1	0;0;100	1.27	True		ENSG00000171634	ENSG00000171634	HGNC:3581													
GNB1	gene	GNB1	Expert list;Expert Review;Expert Review Red	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Intellectual developmental disorder, autosomal dominant 42, MIM# 616973				32345733		False	1	0;0;100	1.27	True		ENSG00000078369	ENSG00000078369	HGNC:4396													
HNRNPK	gene	HNRNPK	Expert list;Expert Review;Expert Review Red	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Au-Kline syndrome, MIM# 616580				36117209		False	1	0;0;100	1.27	True		ENSG00000165119	ENSG00000165119	HGNC:5044													
KDM5C	gene	KDM5C	Expert list;Expert Review;Expert Review Red	Speech apraxia		Neurology and neurodevelopmental disorders	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Intellectual developmental disorder, X-linked syndromic, Claes-Jensen type, MIM# 300534				36117209;36434256		False	1	0;0;100	1.27	True		ENSG00000126012	ENSG00000126012	HGNC:11114													
PHF21A	gene	PHF21A	Expert list;Expert Review;Expert Review Red	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures, MIM# 618725				36117209		False	1	0;0;100	1.27	True		ENSG00000135365	ENSG00000135365	HGNC:24156													
POGZ	gene	POGZ	Expert list;Expert Review;Expert Review Red	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	White-Sutton syndrome, MIM# 616364				32345733;35052493		False	1	0;0;100	1.27	True		ENSG00000143442	ENSG00000143442	HGNC:18801													
PURA	gene	PURA	Expert list;Expert Review;Expert Review Red	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties, MIM# 616158				36117209		False	1	0;0;100	1.27	True		ENSG00000185129	ENSG00000185129	HGNC:9701													
SETD1B	gene	SETD1B	Expert list;Expert Review;Expert Review Red	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Intellectual developmental disorder with seizures and language delay, MIM# 619000				36117209		False	1	0;0;100	1.27	True		ENSG00000139718	ENSG00000139718	HGNC:29187													
SPAST	gene	SPAST	Expert list;Expert Review;Expert Review Red	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Spastic paraplegia 4, autosomal dominant, MIM# 182601				36117209		False	1	0;0;100	1.27	True		ENSG00000021574	ENSG00000021574	HGNC:11233													
TAOK2	gene	TAOK2	Expert list;Expert Review;Expert Review Red	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Neurodevelopmental disorder (MONDO:0700092), TAOK2-related				36117209		False	1	0;0;100	1.27	True		ENSG00000149930	ENSG00000149930	HGNC:16835													
TRIP12	gene	TRIP12	Expert list;Expert Review;Expert Review Red	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Intellectual developmental disorder, autosomal dominant 49, MIM# 617752				36117209		False	1	0;0;100	1.27	True		ENSG00000153827	ENSG00000153827	HGNC:12306													
UPF2	gene	UPF2	Expert list;Expert Review;Expert Review Red	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Neurodevelopmental disorder (MONDO:0700092), UPF2-related				32345733;31585809		False	1	0;0;100	1.27	True		ENSG00000151461	ENSG00000151461	HGNC:17854													
ZBTB18	gene	ZBTB18	Expert list;Expert Review;Expert Review Red	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Intellectual developmental disorder, autosomal dominant 22, MIM# 612337				36117209		False	1	0;0;100	1.27	True		ENSG00000179456	ENSG00000179456	HGNC:13030													
ZFHX4	gene	ZFHX4	Expert list;Expert Review;Expert Review Red	Speech apraxia		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Neurodevelopmental disorder (MONDO:0700092), ZFHX4-related				29463886;34461323		False	1	0;0;100	1.27	True		ENSG00000091656	ENSG00000091656	HGNC:30939