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
FAAHP1	gene	FAAHP1	Expert Review Red;Genomics England PanelApp;Literature	Pain syndromes		Neurology and neurodevelopmental disorders	Unknown	Pain insensitivity			Pain;HP:0012531	30929760		False	1	0;0;100	0.34	True		ENSG00000232022	ENSG00000232022	HGNC:50679													
MPV17	gene	MPV17	Expert Review Red;Genomics England PanelApp	Pain syndromes		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Mitochondrial DNA depletion syndrome 6 (hepatocerebral type), 256810;Navajo neurohepatopathy;Pain insensitivity			Pain;HP:0012531	16582910;16909392;23714749;22508010;185990;11431741		False	1	0;0;100	0.34	True		ENSG00000115204	ENSG00000115204	HGNC:7224													
PLEKHN1	gene	PLEKHN1	Expert Review Red;Literature	Pain syndromes		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Sensory Neuropathy			Pain;HP:0012531	33884296		False	1	0;0;0	0.34	True		ENSG00000187583	ENSG00000187583	HGNC:25284													
SMPDL3A	gene	SMPDL3A	Expert Review Red;Literature	Pain syndromes		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Sensory Neuropathy			Pain;HP:0012531	33884296		False	1	0;0;100	0.34	True		ENSG00000172594	ENSG00000172594	HGNC:17389													
TRPV1	gene	TRPV1	Expert Review Red;Literature	Pain syndromes		Neurology and neurodevelopmental disorders	BIALLELIC, autosomal or pseudoautosomal	Channelopathy-associated congenital insensitivity to pain, autosomal recessive - MONDO:0009459			Pain;HP:0012531	PMID: 36454632;PMID: 36472910		False	1	0;0;100	0.34	True		ENSG00000196689	ENSG00000196689	HGNC:12716