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
ARHGAP36	gene	ARHGAP36	Expert Review;Expert Review Amber	Hair disorders		Dermatological disorders	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	"Bazex-Dupre-Christol syndrome, MIM#	301845"			Abnormal hair morphology;HP:0001595	35986704;40015599		False	2	0;100;0	0.89	True	Other	ENSG00000147256	ENSG00000147256	HGNC:26388													
C3orf52	gene	C3orf52	Expert Review Amber;Literature	Hair disorders		Dermatological disorders	BIALLELIC, autosomal or pseudoautosomal	Hypotrichosis-15, MIM#620177			Abnormal hair morphology;HP:0001595	PMID: 32336749		False	2	0;100;0	0.89	True		ENSG00000114529	ENSG00000114529	HGNC:26255													
CST6	gene	CST6	Expert list;Expert Review Amber	Hair disorders		Dermatological disorders	BIALLELIC, autosomal or pseudoautosomal	Ectodermal dysplasia 15, hypohidrotic/hair type MIM#618535			Abnormal hair morphology;HP:0001595	30425301;12393798;36371786		False	2	0;100;0	0.89	True		ENSG00000175315	ENSG00000175315	HGNC:2478													
DSC3	gene	DSC3	Expert Review Amber;NHS GMS	Hair disorders		Dermatological disorders	BIALLELIC, autosomal or pseudoautosomal	Hypotrichosis and recurrent skin vesicles MIM#613102			Abnormal hair morphology;HP:0001595	19765682;31790667;18682494		False	2	0;100;0	0.89	True		ENSG00000134762	ENSG00000134762	HGNC:3037													
KDF1	gene	KDF1	Expert list;Expert Review Amber	Hair disorders		Dermatological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail type MIM#617337			Abnormal hair morphology;HP:0001595	27838789;24075906		False	2	0;100;0	0.89	True		ENSG00000175707	ENSG00000175707	HGNC:26624													
KRT71	gene	KRT71	Expert Review Amber;Literature	Hair disorders		Dermatological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	?Hypotrichosis 13, 615896			Abnormal hair morphology;HP:0001595	31332722;14632181;22592156;19713490		False	2	0;100;0	0.89	True		ENSG00000139648	ENSG00000139648	HGNC:28927													
KRT74	gene	KRT74	Expert Review Amber;NHS GMS;Royal Melbourne Hospital	Hair disorders		Dermatological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Hypotrichosis 3 , MIM# 613981;Woolly hair, autosomal dominant, MIM# 194300			Abnormal hair morphology;HP:0001595	21188418;20346438;21188418		False	2	0;100;0	0.89	True		ENSG00000170484	ENSG00000170484	HGNC:28929													
KRT83	gene	KRT83	Expert Review Amber;Literature	Hair disorders		Dermatological disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Monilethrix, MIM#621170			Abnormal hair morphology;HP:0001595	31332722;15744029;25557232		False	2	0;100;0	0.89	True		ENSG00000170523	ENSG00000170523	HGNC:6460													
TARS	gene	TARS	Expert Review Amber;Literature	Hair disorders		Dermatological disorders	BIALLELIC, autosomal or pseudoautosomal	Trichothiodystrophy 7, nonphotosensitive, 618546			Abnormal hair morphology;HP:0001595	31332722;31374204		False	2	0;100;0	0.89	True		ENSG00000113407	ENSG00000113407	HGNC:11572													
TGM3	gene	TGM3	Expert Review Amber;Literature	Hair disorders		Dermatological disorders	BIALLELIC, autosomal or pseudoautosomal	?Uncombable hair syndrome 2, 617251			Abnormal hair morphology;HP:0001595	31332722		False	2	0;100;0	0.89	True		ENSG00000125780	ENSG00000125780	HGNC:11779