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
APOA1	gene	APOA1	Expert list;Expert Review Green	Amyloidosis			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Amyloidosis, 3 or more types, MIM#105200			Renal amyloidosis;HP:0001917; Amyloidosis;HP:0011034	PubMed:31482740;29968409;27240838		False	3	100;0;0	1.1	True		ENSG00000118137	ENSG00000118137	HGNC:600													
APOA4	gene	APOA4	Expert Review Green;Literature	Amyloidosis			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"Hereditary amyloidosis, MONDO:0018634, APOA4-related;Tubulointerstitial kidney disease, autosomal dominant 6, MIM#	621106"			Renal amyloidosis;HP:0001917; Amyloidosis;HP:0011034	PMID: 38096951		False	3	100;0;0	1.1	True		ENSG00000110244	ENSG00000110244	HGNC:602													
B2M	gene	B2M	Expert Review Green;Literature;Victorian Clinical Genetics Services	Amyloidosis			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"variant ABeta2M amyloidosis	MONDO:0017810"			Renal amyloidosis;HP:0001917; Amyloidosis;HP:0011034	22693999;37223323;24014031;35575118;32875920		False	3	100;0;0	1.1	False		ENSG00000166710	ENSG00000166710	HGNC:914													
FGA	gene	FGA	Expert list;Expert Review Green	Amyloidosis			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Amyloidosis, familial visceral, MIM#105200			Renal amyloidosis;HP:0001917; Amyloidosis;HP:0011034	PubMed: 8097946;8639778;12050338;31064749;17295221;19073821;11739173		False	3	100;0;0	1.1	True		ENSG00000171560	ENSG00000171560	HGNC:3661													
GPNMB	gene	GPNMB	Expert Review Green;Other;Victorian Clinical Genetics Services	Amyloidosis			BIALLELIC, autosomal or pseudoautosomal	amyloidosis, primary localized cutaneous, 3 MONDO:0054765			Renal amyloidosis;HP:0001917; Amyloidosis;HP:0011034	29336782		False	3	100;0;0	1.1	True		ENSG00000136235	ENSG00000136235	HGNC:4462													
GSN	gene	GSN	Expert list;Expert Review Green;Victorian Clinical Genetics Services	Amyloidosis			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Amyloidosis, Finnish type, MIM#105200			Renal amyloidosis;HP:0001917; Amyloidosis;HP:0011034	PubMed: 8395367;2176164;8684801;6975851;29167514		False	3	100;0;0	1.1	True		ENSG00000148180	ENSG00000148180	HGNC:4620													
LYZ	gene	LYZ	Expert list;Expert Review Green	Amyloidosis			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Amyloidosis, renal, MIM#105200			Renal amyloidosis;HP:0001917; Amyloidosis;HP:0011034	PubMed: 1808634;8464497;15745733,		False	3	100;0;0	1.1	True		ENSG00000090382	ENSG00000090382	HGNC:6740													
NLRP3	gene	NLRP3	Expert list;Expert Review Green	Amyloidosis			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Muckle-Wells syndrome, MIM#191900			Renal amyloidosis;HP:0001917; Amyloidosis;HP:0011034	PubMed: 11687797;28229991;27435956;31057541		False	3	100;0;0	1.1	True		ENSG00000162711	ENSG00000162711	HGNC:16400													
OSMR	gene	OSMR	Expert Review Green;Other	Amyloidosis			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	primary cutaneous amyloidosis MONDO:0015301			Renal amyloidosis;HP:0001917; Amyloidosis;HP:0011034	19375894;19528426;25054142;20507362;19690585		False	3	100;0;0	1.1	True		ENSG00000145623	ENSG00000145623	HGNC:8507													
TTR	gene	TTR	Expert Review Green;Literature	Amyloidosis			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	hereditary ATTR amyloidosis MONDO:0017132			Renal amyloidosis;HP:0001917; Amyloidosis;HP:0011034	20301373;38484868		False	3	100;0;0	1.1	True		ENSG00000118271	ENSG00000118271	HGNC:12405													
APOC2	gene	APOC2	Expert Review Amber;Literature	Amyloidosis			MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	APOC2-related amyloidosis, MONDO:0019065			Renal amyloidosis;HP:0001917; Amyloidosis;HP:0011034	39547356;27297947;27840752;30686043;30197986		False	2	0;100;0	1.1	True		ENSG00000234906	ENSG00000234906	HGNC:609													
