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	Expert Review Amber;Genomics England PanelApp	Pain syndromes		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Neuropathy, hereditary sensory, with spastic paraplegia, 256840;HSAN with spastic paraplegia			Pain;HP:0012531	12874111;16399879;25124038;28623285		False	2	0;100;0	0.34	True		ENSG00000150753	ENSG00000150753	HGNC:1618													
CLTCL1	gene	CLTCL1	Expert Review Amber;Genomics England PanelApp;Literaure;Review	Pain syndromes		Neurology and neurodevelopmental disorders	Unknown	Congenital insensitivity to pain			Pain;HP:0012531	26068709;29402896		False	2	0;100;0	0.34	True		ENSG00000070371	ENSG00000070371	HGNC:2093													
NAGLU	gene	NAGLU	Expert Review Amber;Genomics England PanelApp	Pain syndromes		Neurology and neurodevelopmental disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Mucopolysaccharidosis type IIIB (Sanfilippo B), AR, 252920;Late-onset painful sensory neuropathy, AD			Pain;HP:0012531	25818867;12202988		False	2	0;100;0	0.34	True		ENSG00000108784	ENSG00000108784	HGNC:7632													
NMNAT2	gene	NMNAT2	Expert Review Amber;Genomics England PanelApp;Research	Pain syndromes		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	polyneuropathy;erythromelalgia			Pain;HP:0012531	31132363;25271157;20126265		False	2	0;100;0	0.34	True		ENSG00000157064	ENSG00000157064	HGNC:16789													
TRPA1	gene	TRPA1	Expert Review Amber;Genomics England PanelApp	Pain syndromes		Neurology and neurodevelopmental disorders	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Familial episodic pain syndrome type I;Episodic pain syndrome, familial,  615040			Pain;HP:0012531	28314413;21468319;24778270;20718100;16564016;28436534;24564660;20547126		False	2	0;100;0	0.34	True		ENSG00000104321	ENSG00000104321	HGNC:497