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
CFTR	gene	CFTR	Expert Review Green;Victorian Clinical Genetics Services	Pancreatitis		Gastroenterological disorders	BIALLELIC, autosomal or pseudoautosomal	Cystic fibrosis			Pancreatitis;HP:0001733			False	3	100;0;0	1.6	True		ENSG00000001626	ENSG00000001626	HGNC:1884													
CPA1	gene	CPA1	Expert Review Green;Victorian Clinical Genetics Services	Pancreatitis		Gastroenterological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Hereditary pancreatitis, MONDO:0008185, CPA1-related			Pancreatitis;HP:0001733	23955596;28497564;28258133;31005883		False	3	100;0;0	1.6	True		ENSG00000091704	ENSG00000091704	HGNC:2296													
PRSS1	gene	PRSS1	Expert Review Green;Victorian Clinical Genetics Services	Pancreatitis		Gastroenterological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Pancreatitis, hereditary, MIM# 167800			Pancreatitis;HP:0001733	8841182;10204851;10529393;11097832;11702203;15776435;16791840;18461367;17072318		False	3	100;0;0	1.6	True		ENSG00000204983	ENSG00000204983	HGNC:9475													
SPINK1	gene	SPINK1	Expert Review Green;Victorian Clinical Genetics Services	Pancreatitis		Gastroenterological disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Tropical calcific pancreatitis, MIM# 608189;Pancreatitis, hereditary, MIM# 167800			Pancreatitis;HP:0001733	10835640;11355022;11938439;16823394;17274009;27535533		False	3	100;0;0	1.6	True		ENSG00000164266	ENSG00000164266	HGNC:11244													
TRPV6	gene	TRPV6	Expert Review Green;Literature	Pancreatitis		Gastroenterological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Early onset chronic pancreatitis susceptibility			Pancreatitis;HP:0001733	32383311;31930989		False	3	100;0;0	1.6	True		ENSG00000165125	ENSG00000165125	HGNC:14006													
CASR	gene	CASR	Expert Review Amber;Victorian Clinical Genetics Services	Pancreatitis		Gastroenterological disorders	Other	Susceptibility to pancreatitis			Pancreatitis;HP:0001733	16497624;26166472		False	2	0;100;0	1.6	True		ENSG00000036828	ENSG00000036828	HGNC:1514													
CELA3B	gene	CELA3B	Expert Review Amber;Literature	Pancreatitis		Gastroenterological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Chronic pancreatitis			Pancreatitis;HP:0001733	31369399;33565216		False	2	0;100;0	1.6	True	Other	ENSG00000219073	ENSG00000219073	HGNC:15945													
CTRC	gene	CTRC	Expert Review Amber;Victorian Clinical Genetics Services	Pancreatitis		Gastroenterological disorders	Other	{Pancreatitis, chronic, susceptibility to}, MIM#167800			Pancreatitis;HP:0001733	18059268;18172691;28502372		False	2	0;100;0	1.6	True		ENSG00000162438	ENSG00000162438	HGNC:2523