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
FBXW11	gene	FBXW11	Expert Review Red;Literature	Autoinflammatory Disorders		Immunological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Autoinflammatory disorder MONDO:0019751, FBXW11-related				PMID: 36250618		False	1	0;0;100	2.3	True		ENSG00000072803	ENSG00000072803	HGNC:13607													
IL1R1	gene	IL1R1	Expert Review Red;Literature	Autoinflammatory Disorders		Immunological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"Chronic recurrent multifocal osteomyelitis 3, MIM#	259680"				37315560		False	1	0;0;100	2.3	True		ENSG00000115594	ENSG00000115594	HGNC:5993													
IL6ST	gene	IL6ST	Expert Review Red;Literature	Autoinflammatory Disorders		Immunological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"Immunodeficiency 94 with autoinflammation and dysmorphic facies 	619750"				33517393		False	1	0;0;100	2.3	True		ENSG00000134352	ENSG00000134352	HGNC:6021													
IRAK2	gene	IRAK2	Expert Review Red;Literature	Autoinflammatory Disorders		Immunological disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Immune dysregulation, MONDO:0957790, IRAK2-related				PMID: 39299377		False	1	0;0;100	2.3	True		ENSG00000134070	ENSG00000134070	HGNC:6113													
LSM11	gene	LSM11	Expert list;Expert Review Red	Autoinflammatory Disorders		Immunological disorders	BIALLELIC, autosomal or pseudoautosomal	Aicardi-Goutieres syndrome MONDO:0018866				33230297		False	1	0;0;100	2.3	True		ENSG00000155858	ENSG00000155858	HGNC:30860													
PSMA5	gene	PSMA5	Expert Review Red;Literature	Autoinflammatory Disorders		Immunological disorders	Other	Inborn error of immunity, MONDO:0003778, PSMA5-related;PRAAS/CANDLE				PMID: 37600812		False	1	0;0;100	2.3	True		ENSG00000143106	ENSG00000143106	HGNC:9534													
PSMG2	gene	PSMG2	Expert list;Expert Review Red	Autoinflammatory Disorders		Immunological disorders	BIALLELIC, autosomal or pseudoautosomal	"Proteasome-associated autoinflammatory syndrome 4, MIM#	619183;CANDLE syndrome;Chronic atypical neutrophilic dermatitis with lipodystrophy"				30664889		False	1	0;0;100	2.3	True		ENSG00000128789	ENSG00000128789	HGNC:24929													
SIRT1	gene	SIRT1	Expert Review Red;Literature	Autoinflammatory Disorders		Immunological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	autoimmune disease, MONDO:0007179, SIRT1-related				23473037		False	1	0;0;100	2.3	True		ENSG00000096717	ENSG00000096717	HGNC:14929