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 PDGFRA gene PDGFRA Literature Adult solid tumours for rare disease Tumour syndromes Tumour syndromes MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Gastrointestinal stromal tumor/GIST-plus syndrome, somatic or familial, OMIM:175510 False 1 0;100;0 1.40 False ENSG00000134853 ENSG00000134853 HGNC:8803