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
ARHGAP42	gene	ARHGAP42	Expert Review Red;Literature	Pulmonary Fibrosis_Interstitial Lung Disease		Respiratory disorders	BIALLELIC, autosomal or pseudoautosomal	Interstitial lung disease;systemic hypertension;immunological abnormalities			Pulmonary fibrosis;HP:0002206; Abnormal pulmonary interstitial morphology;HP:0006530	34232960		False	1	0;0;100	1.11	True		ENSG00000165895	ENSG00000165895	HGNC:26545													
ASAH1	gene	ASAH1	Expert Review Red;Victorian Clinical Genetics Services	Pulmonary Fibrosis_Interstitial Lung Disease		Respiratory disorders	Unknown	Spinal muscular atrophy with progressive myoclonic epilepsy, MIM# 159950;Farber lipogranulomatosis, MIM# 228000			Pulmonary fibrosis;HP:0002206; Abnormal pulmonary interstitial morphology;HP:0006530	32875576;32449975		False	1	0;0;100	1.11	True		ENSG00000104763	ENSG00000104763	HGNC:735													
BMPR1B	gene	BMPR1B	Expert list;Expert Review Red	Pulmonary Fibrosis_Interstitial Lung Disease		Respiratory disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Pulmonary arterial hypertension, MONDO:0015924			Pulmonary fibrosis;HP:0002206; Abnormal pulmonary interstitial morphology;HP:0006530	22374147;28768485		False	1	0;50;50	1.11	True	Other	ENSG00000138696	ENSG00000138696	HGNC:1077													
CARD11	gene	CARD11	Expert list;Expert Review Red	Pulmonary Fibrosis_Interstitial Lung Disease		Respiratory disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	"Immunodeficiency 11B with atopic dermatitis, MIM#	617638;HIES (Job syndrome);Bronchiectasis"			Pulmonary fibrosis;HP:0002206; Abnormal pulmonary interstitial morphology;HP:0006530	28628108;28826773		False	1	0;0;100	1.11	True		ENSG00000198286	ENSG00000198286	HGNC:16393													
FOXP1	gene	FOXP1	Expert Review Red;Victorian Clinical Genetics Services	Pulmonary Fibrosis_Interstitial Lung Disease		Respiratory disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Hypotonia, developmental delay, atrial septal defect - neuroendocrine hyperplasia of infancy (NEHI)			Pulmonary fibrosis;HP:0002206; Abnormal pulmonary interstitial morphology;HP:0006530	28884888		False	1	0;0;100	1.11	True		ENSG00000114861	ENSG00000114861	HGNC:3823													
GDNF	gene	GDNF	Expert Review Red;Victorian Clinical Genetics Services	Pulmonary Fibrosis_Interstitial Lung Disease		Respiratory disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Central hypoventilation syndrome, MIM# 209880			Pulmonary fibrosis;HP:0002206; Abnormal pulmonary interstitial morphology;HP:0006530			False	1	0;0;100	1.11	True		ENSG00000168621	ENSG00000168621	HGNC:4232													
HPS6	gene	HPS6	Expert Review Red;Victorian Clinical Genetics Services	Pulmonary Fibrosis_Interstitial Lung Disease		Respiratory disorders	BIALLELIC, autosomal or pseudoautosomal	"Hermansky-Pudlak syndrome 6, MIM#	614075"			Pulmonary fibrosis;HP:0002206; Abnormal pulmonary interstitial morphology;HP:0006530			False	1	0;0;100	1.11	True		ENSG00000166189	ENSG00000166189	HGNC:18817													
MUC5B	gene	MUC5B	Expert Review Red;Victorian Clinical Genetics Services	Pulmonary Fibrosis_Interstitial Lung Disease		Respiratory disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	{Pulmonary fibrosis, idiopathic, susceptibility to}, MIM# 178500			Pulmonary fibrosis;HP:0002206; Abnormal pulmonary interstitial morphology;HP:0006530	21506741;21506748		False	1	0;0;100	1.11	False		ENSG00000117983	ENSG00000117983	HGNC:7516													
RET	gene	RET	Expert Review Red;Victorian Clinical Genetics Services	Pulmonary Fibrosis_Interstitial Lung Disease		Respiratory disorders	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Central hypoventilation syndrome, congenital, MIM#209880			Pulmonary fibrosis;HP:0002206; Abnormal pulmonary interstitial morphology;HP:0006530	18438890;16443855;12566528;12086152		False	1	0;0;100	1.11	True		ENSG00000165731	ENSG00000165731	HGNC:9967													
RPA2	gene	RPA2	Expert Review Red;Literature	Pulmonary Fibrosis_Interstitial Lung Disease		Respiratory disorders	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Telomere syndrome, MONDO:0100137, RPA2-related			Pulmonary fibrosis;HP:0002206; Abnormal pulmonary interstitial morphology;HP:0006530	41703052;39231615		False	1	0;0;100	1.11	True		ENSG00000117748	ENSG00000117748	HGNC:10290													
S100A13	gene	S100A13	Expert Review Red;Literature	Pulmonary Fibrosis_Interstitial Lung Disease		Respiratory disorders	BIALLELIC, autosomal or pseudoautosomal	Pulmonary fibrosis, MONDO:0002771, S100A13-related			Pulmonary fibrosis;HP:0002206; Abnormal pulmonary interstitial morphology;HP:0006530	40497957;38099297;31073086		False	1	0;0;100	1.11	True		ENSG00000189171	ENSG00000189171	HGNC:10490													
S100A3	gene	S100A3	Expert Review Red;Literature	Pulmonary Fibrosis_Interstitial Lung Disease		Respiratory disorders	BIALLELIC, autosomal or pseudoautosomal	Pulmonary fibrosis, MONDO:0002771, S100A3-related			Pulmonary fibrosis;HP:0002206; Abnormal pulmonary interstitial morphology;HP:0006530	40497957;38099297;31073086		False	1	0;0;100	1.11	True		ENSG00000188015	ENSG00000188015	HGNC:10493													
ZNF341	gene	ZNF341	Expert list;Expert Review Red	Pulmonary Fibrosis_Interstitial Lung Disease		Respiratory disorders	BIALLELIC, autosomal or pseudoautosomal	Hyper-IgE recurrent infection syndrome 3, autosomal recessive, MIM# 618282;Bronchiectasis			Pulmonary fibrosis;HP:0002206; Abnormal pulmonary interstitial morphology;HP:0006530	29907691;29907690		False	1	0;0;100	1.11	True		ENSG00000131061	ENSG00000131061	HGNC:15992