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
COL7A1	gene	COL7A1	Expert Review Red;Victorian Clinical Genetics Services	Inflammatory bowel disease		Gastroenterological disorders	BIALLELIC, autosomal or pseudoautosomal	Epidermolysis bullosa dystrophica, AR, MIM# 226600			Gastrointestinal inflammation;HP:0004386	27537055;25058236		False	1	0;0;100	0.122	True		ENSG00000114270	ENSG00000114270	HGNC:2214													
FERMT1	gene	FERMT1	Expert Review Red;Victorian Clinical Genetics Services	Inflammatory bowel disease		Gastroenterological disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Kindler syndrome, MIM# 173650			Gastrointestinal inflammation;HP:0004386	19057668;27537055;32463623		False	1	0;0;100	0.122	True		ENSG00000101311	ENSG00000101311	HGNC:15889													
FMNL2	gene	FMNL2	Expert Review Red;Literature	Inflammatory bowel disease		Gastroenterological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	inflammatory bowel disease, MONDO:0005265, FMNL2-related			Gastrointestinal inflammation;HP:0004386	34043722		False	1	0;0;100	0.122	True		ENSG00000157827	ENSG00000157827	HGNC:18267													
IL21	gene	IL21	Expert Review;Expert Review Red	Inflammatory bowel disease		Gastroenterological disorders	BIALLELIC, autosomal or pseudoautosomal	Immunodeficiency, common variable, 11, MIM# 615767			Gastrointestinal inflammation;HP:0004386	24746753		False	1	0;100;0	0.122	True		ENSG00000138684	ENSG00000138684	HGNC:6005													
IL37	gene	IL37	Expert Review Red;Literature	Inflammatory bowel disease		Gastroenterological disorders	BIALLELIC, autosomal or pseudoautosomal	"Inflammatory bowel disease (infantile ulcerative colitis) 31, MIM#	619398"			Gastrointestinal inflammation;HP:0004386	33674380		False	1	0;0;100	0.122	True		ENSG00000125571	ENSG00000125571	HGNC:15563													
LY96	gene	LY96	Expert Review Red;Literature	Inflammatory bowel disease		Gastroenterological disorders	BIALLELIC, autosomal or pseudoautosomal	Inborn error of immunity, MONDO:0003778, LY96-related;Colitis			Gastrointestinal inflammation;HP:0004386	PMID: 36462957		False	1	0;0;100	0.122	True		ENSG00000154589	ENSG00000154589	HGNC:17156													
PMM2	gene	PMM2	Expert Review Red;Literature	Inflammatory bowel disease		Gastroenterological disorders	BIALLELIC, autosomal or pseudoautosomal	"Congenital disorder of glycosylation, type Ia, MIM#	212065;Inflammatory bowel disease, hyperinsulinism, polycystic kidney disease"			Gastrointestinal inflammation;HP:0004386	36773065		False	1	0;0;100	0.122	True		ENSG00000140650	ENSG00000140650	HGNC:9115													
PTEN	gene	PTEN	Expert Review Red;Victorian Clinical Genetics Services	Inflammatory bowel disease		Gastroenterological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Colitis			Gastrointestinal inflammation;HP:0004386	23962154;24882466;25352295;22266152		False	1	0;50;50	0.122	True		ENSG00000171862	ENSG00000171862	HGNC:9588