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
MBTPS2	gene	MBTPS2	Expert Review Green;Other	Familial cicatricial alopecia	Skin adnexa disorders	Dermatological disorders	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Keratosis follicularis spinulosa decalvans, X-linked, 208800 (includes progressive cicatricial alopecia of the scalp);KFSDX;scarring alopecia				22816986;20672378;23316014		False	3	100;0;0	1.6	False		ENSG00000012174	ENSG00000012174	HGNC:15455													
HLA-DRA	gene	HLA-DRA	Expert Review Amber;Other	Familial cicatricial alopecia	Skin adnexa disorders	Dermatological disorders	Unknown	Graham Little-Piccardi-Lassueur syndrome; Graham Little syndrome; lichen planopilaris; progressive cicatricial (scarring) alopecia						False	2	0;100;0	1.6	False		ENSG00000204287	ENSG00000204287	HGNC:4947													
SDR9C7	gene	SDR9C7	Expert Review Amber;Other	Familial cicatricial alopecia	Skin adnexa disorders	Dermatological disorders	BIALLELIC, autosomal or pseudoautosomal	autosomal recessive congenital ichthyosis (ARCI) type 7 (includes scarring alopecia)						False	2	0;100;0	1.6	False		ENSG00000170426	ENSG00000170426	HGNC:29958