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
ADCY1	gene	ADCY1	Expert Review Red;Melbourne Genomics Health Alliance Deafness Flagship;Victorian Clinical Genetics Services	Deafness_IsolatedAndComplex		Hearing and ear disorders	BIALLELIC, autosomal or pseudoautosomal	Deafness, autosomal recessive 44, MIM# 610154			Hearing impairment;HP:0000365	24482543		False	1	0;0;100	1.210	True		ENSG00000164742	ENSG00000164742	HGNC:232													
BDP1	gene	BDP1	Expert Review Red;Melbourne Genomics Health Alliance Deafness Flagship;Victorian Clinical Genetics Services	Deafness_IsolatedAndComplex		Hearing and ear disorders	BIALLELIC, autosomal or pseudoautosomal	Deafness, autosomal recessive 112, MIM#618257			Hearing impairment;HP:0000365	24312468;25060281		False	1	0;0;100	1.210	True		ENSG00000145734	ENSG00000145734	HGNC:13652													
CATSPER2	gene	CATSPER2	Expert Review Red;Melbourne Genomics Health Alliance Deafness Flagship;Victorian Clinical Genetics Services	Deafness_IsolatedAndComplex		Hearing and ear disorders	Unknown				Hearing impairment;HP:0000365			False	1	0;0;100	1.210	True		ENSG00000166762	ENSG00000166762	HGNC:18810													
CNRIP1	gene	CNRIP1	Expert Review Red;Literature	Deafness_IsolatedAndComplex		Hearing and ear disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"Deafness, autosomal dominant 58	MIM#615654"			Hearing impairment;HP:0000365	32337552;19159392		False	1	0;0;100	1.210	True		ENSG00000119865	ENSG00000119865	HGNC:24546													
DCDC2	gene	DCDC2	Expert list;Expert Review Red	Deafness_IsolatedAndComplex		Hearing and ear disorders	BIALLELIC, autosomal or pseudoautosomal	"Deafness, autosomal recessive 66, MIM#	610212"			Hearing impairment;HP:0000365	25601850;22558177;25130614		False	1	0;0;100	1.210	True		ENSG00000146038	ENSG00000146038	HGNC:18141													
ELMOD3	gene	ELMOD3	Expert Review Red;Melbourne Genomics Health Alliance Deafness Flagship;Victorian Clinical Genetics Services	Deafness_IsolatedAndComplex		Hearing and ear disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Deafness, autosomal recessive 88, MIM# 615429;Deafness, autosomal dominant 81, MIM# 619500			Hearing impairment;HP:0000365	24039609;31628468;30284680;29713870		False	1	0;0;100	1.210	True		ENSG00000115459	ENSG00000115459	HGNC:26158													
FOXL1	gene	FOXL1	Expert Review Red;Literature	Deafness_IsolatedAndComplex		Hearing and ear disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Otosclerosis 11 #MIM620576			Hearing impairment;HP:0000365	PMID: 34633540		False	1	0;0;100	1.210	True		ENSG00000176678	ENSG00000176678	HGNC:3817													
GJB3	gene	GJB3	Expert Review Red;Melbourne Genomics Health Alliance Deafness Flagship;Victorian Clinical Genetics Services	Deafness_IsolatedAndComplex		Hearing and ear disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Deafness, autosomal dominant 2B, MIM# 612644			Hearing impairment;HP:0000365	9843210		False	1	0;0;100	1.210	True		ENSG00000188910	ENSG00000188910	HGNC:4285													
GJB4	gene	GJB4	Expert Review Red;Melbourne Genomics Health Alliance Deafness Flagship;Victorian Clinical Genetics Services	Deafness_IsolatedAndComplex		Hearing and ear disorders	Unknown	Deafness			Hearing impairment;HP:0000365			False	1	0;0;100	1.210	True		ENSG00000189433	ENSG00000189433	HGNC:4286													
GRAP	gene	GRAP	Expert list;Expert Review Red	Deafness_IsolatedAndComplex		Hearing and ear disorders	BIALLELIC, autosomal or pseudoautosomal	"Deafness, autosomal recessive 114, MIM#	618456"			Hearing impairment;HP:0000365	30610177		False	1	0;0;100	1.210	True		ENSG00000154016	ENSG00000154016	HGNC:4562													
HARS	gene	HARS	Expert Review Red;Melbourne Genomics Health Alliance Deafness Flagship;Victorian Clinical Genetics Services	Deafness_IsolatedAndComplex		Hearing and ear disorders	BIALLELIC, autosomal or pseudoautosomal	Usher syndrome type 3B, MIM# 614504			Hearing impairment;HP:0000365	22279524		False	1	0;0;100	1.210	True		ENSG00000170445	ENSG00000170445	HGNC:4816													
MCM2	gene	MCM2	Expert list;Expert Review Red	Deafness_IsolatedAndComplex		Hearing and ear disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Deafness, autosomal dominant 70, MIM# 616968			Hearing impairment;HP:0000365	26196677		False	1	0;0;100	1.210	True		ENSG00000073111	ENSG00000073111	HGNC:6944													
MET	gene	MET	Expert list;Expert Review Red	Deafness_IsolatedAndComplex		Hearing and ear disorders	BIALLELIC, autosomal or pseudoautosomal	"Deafness, autosomal recessive 97, MIM#	616705"			Hearing impairment;HP:0000365	25941349;31801140		False	1	0;0;100	1.210	True		ENSG00000105976	ENSG00000105976	HGNC:7029													
NAT6	gene	NAT6	Expert Review Red;Literature	Deafness_IsolatedAndComplex		Hearing and ear disorders	BIALLELIC, autosomal or pseudoautosomal	"Auroneurodental syndrome, MIM# 	620830"			Hearing impairment;HP:0000365	34805998		False	1	0;0;100	1.210	True		ENSG00000243477	ENSG00000243477	HGNC:30252													
NR2F1	gene	NR2F1	Expert Review Red;Melbourne Genomics Health Alliance Deafness Flagship;Victorian Clinical Genetics Services	Deafness_IsolatedAndComplex		Hearing and ear disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Bosch-Boonstra-Schaaf optic atrophy syndrome, MIM# 615722			Hearing impairment;HP:0000365	19353646;24462372		False	1	0;0;100	1.210	True		ENSG00000175745	ENSG00000175745	HGNC:7975													
SCD5	gene	SCD5	Expert list;Expert Review Red	Deafness_IsolatedAndComplex		Hearing and ear disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Deafness, autosomal dominant 79, MIM#619086			Hearing impairment;HP:0000365	31972369		False	1	0;0;100	1.210	True		ENSG00000145284	ENSG00000145284	HGNC:21088													
SIX5	gene	SIX5	Expert Review Red;Melbourne Genomics Health Alliance Deafness Flagship;Victorian Clinical Genetics Services	Deafness_IsolatedAndComplex		Hearing and ear disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Branchiootorenal syndrome 2, MIM#610896			Hearing impairment;HP:0000365	17357085;24429398;21280147;14704431;17357085;11950062		False	1	0;0;100	1.210	True		ENSG00000177045	ENSG00000177045	HGNC:10891													
TBL1Y	gene	TBL1Y	Expert Review Red;Literature	Deafness_IsolatedAndComplex		Hearing and ear disorders	Other	Deafness, Y-linked 2, MIM# 400047			Hearing impairment;HP:0000365	30341416		False	1	0;0;100	1.210	True		ENSG00000092377	ENSG00000092377	HGNC:18502													
TJP2	gene	TJP2	Expert Review Red;Melbourne Genomics Health Alliance Deafness Flagship;Victorian Clinical Genetics Services	Deafness_IsolatedAndComplex		Hearing and ear disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Deafness			Hearing impairment;HP:0000365	24752540;20602916;18616530		False	1	0;0;100	1.210	True		ENSG00000119139	ENSG00000119139	HGNC:11828													
TSPEAR	gene	TSPEAR	Expert Review Red;Melbourne Genomics Health Alliance Deafness Flagship;Victorian Clinical Genetics Services	Deafness_IsolatedAndComplex		Hearing and ear disorders	BIALLELIC, autosomal or pseudoautosomal	Deafness, autosomal recessive 98, MIM#614861			Hearing impairment;HP:0000365	22678063;26969326		False	1	0;0;100	1.210	True		ENSG00000175894	ENSG00000175894	HGNC:1268