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
FICD	gene	FICD	Expert Review Amber;Literature	Monogenic diabetes		Endocrinology	BIALLELIC, autosomal or pseudoautosomal	Spastic paraplegia 92, autosomal recessive, OMIM:620911;diabetes mellitus, MONDO:0005015;Neonatal insulin-dependent diabetes mellitus, HP:0000857				36704923;36136088;40062579		False	2	100;0;0	3.22	False		ENSG00000198855	ENSG00000198855	HGNC:18416													
KBTBD2	gene	KBTBD2	Expert Review Amber;Literature	Monogenic diabetes		Endocrinology	BIALLELIC, autosomal or pseudoautosomal	Neurodevelopmental disorder, MONDO:0700092				39313616		False	2	0;100;0	3.22	False		ENSG00000170852	ENSG00000170852	HGNC:21751													
MAFA	gene	MAFA	Expert Review;Expert Review Amber	Monogenic diabetes		Endocrinology	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Insulinomatosis and diabetes mellitus, OMIM:147630;islet cell adenomatosis, MONDO:0007834				17682063;29339498;34644565;35406570		False	2	100;0;0	3.22	False		ENSG00000182759	ENSG00000182759	HGNC:23145													
POC5	gene	POC5	Expert Review Amber;Literature	Monogenic diabetes		Endocrinology	BIALLELIC, autosomal or pseudoautosomal	Retinal dystrophy;diabetes mellitus;lipodystrophy;renal failure;abnormal muscle physiology				29272404;40590205		False	2	100;0;0	3.22	False		ENSG00000152359	ENSG00000152359	HGNC:26658													
SLC19A2	gene	SLC19A2	Expert Review Amber	Monogenic diabetes		Endocrinology	BIALLELIC, autosomal or pseudoautosomal	Thiamine-responsive megaloblastic anemia syndrome, OMIM:249270;diabetes mellitus, MONDO:0005015				26549656;26839896;33571483;39025920;20301459;10391221;38932873		False	2	75;0;25	3.22	False		ENSG00000117479	ENSG00000117479	HGNC:10938													
ZNF808	gene	ZNF808	Expert Review;Expert Review Amber	Monogenic diabetes		Endocrinology	BIALLELIC, autosomal or pseudoautosomal	Pancreatic agenesis 3, OMIM:620991;diabetes mellitus, MONDO:0005015				37973953;41500078		False	2	100;0;0	3.22	False		ENSG00000198482	ENSG00000198482	HGNC:33230													
ISCA-37432-Loss	region		Expert Review Amber	Monogenic diabetes		Endocrinology	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	614527;utero-vaginal atresia;RCAD syndrome;Schizophrenia;Chromosome 17q12 deletion syndrome;delayed development, intellectual disability;global developmental delay;Autism Spectrum Disorder;Renal cysts and diabetes syndrome;Mayer-Rokitansky-Kster-Hauser (MRKH) syndrome in females						False	2	100;0;0	3.22	False					17			36458167	37854616				3		60	cnv_loss	17q12 recurrent (RCAD syndrome) region (includes HNF1B) Loss