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
CCT5	gene	CCT5	Literaure;Review	Pain syndromes	Channelopathies	Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Neuropathy, hereditary sensory, with spastic paraplegia, 256840;HSAN with spastic paraplegia				16399879;25124038;28623285;12874111		False	1	0;0;100	1.12	False		ENSG00000150753	ENSG00000150753	HGNC:1618													
CLTCL1	gene	CLTCL1	Literaure;Review	Pain syndromes	Channelopathies	Neurology and neurodevelopmental disorders	Unknown	Congenital insensitivity to pain				26068709		False	1	0;0;100	1.12	False		ENSG00000070371	ENSG00000070371	HGNC:2093													
FAAHP1	gene	FAAHP1	Literature	Pain syndromes	Channelopathies	Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Pain insensitivity				30929760		False	1	0;0;100	1.12	False		ENSG00000232022	ENSG00000232022	HGNC:50679													
NMNAT2	gene	NMNAT2	Expert Review Red;Research	Pain syndromes	Channelopathies	Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	polyneuropathy;erythromelalgia				31132363		False	1	100;0;0	1.12	False		ENSG00000157064	ENSG00000157064	HGNC:16789