{"context":{"query":">>hgnc>>gencc","source_dataset":"hgnc","target_dataset":"gencc"},"stats":{"queried":6,"total":15,"mapped":4},"pagination":{"has_next":false},"schema":"id|gene_symbol|disease_title|classification_title|moi_title|submitter_title","mappings":[{"input":"HGNC:903","source":"HGNC:903|axin 1","targets":["GENCC_000101-HGNC_903-MONDO_0005484-HP_0000006-GENCC_100004|AXIN1|colorectal adenoma|Limited|Autosomal dominant|Ambry Genetics","GENCC_000112-HGNC_903-OMIM_607864-HP_0000006-GENCC_100004|AXIN1|caudal duplication|Limited|Autosomal dominant|G2P"]},{"input":"HGNC:16421","source":"HGNC:16421|SRY-box transcription factor 6","targets":["GENCC_000101-HGNC_16421-OMIM_618971-HP_0000006-GENCC_100003|SOX6|Tolchin-Le Caignec syndrome|Moderate|Autosomal dominant|Ambry Genetics","GENCC_000105-HGNC_16421-MONDO_0033544-HP_0000006-GENCC_100002|SOX6|Tolchin-Le Caignec syndrome|Strong|Autosomal dominant|Illumina","GENCC_000106-HGNC_16421-OMIM_618971-HP_0000006-GENCC_100002|SOX6|Tolchin-Le Caignec syndrome|Strong|Autosomal dominant|Labcorp Genetics (formerly Invitae)","GENCC_000111-HGNC_16421-OMIM_618971-HP_0000006-GENCC_100002|SOX6|Tolchin-Le Caignec syndrome|Strong|Autosomal dominant|PanelApp Australia","GENCC_000112-HGNC_16421-OMIM_618971-HP_0000006-GENCC_100002|SOX6|Tolchin-Le Caignec syndrome|Strong|Autosomal dominant|G2P"]},{"input":"HGNC:10778","source":"HGNC:10778|secreted frizzled related protein 4","targets":["GENCC_000101-HGNC_10778-OMIM_265900-HP_0000007-GENCC_100003|SFRP4|Pyle disease|Moderate|Autosomal recessive|Ambry Genetics","GENCC_000106-HGNC_10778-OMIM_265900-HP_0000007-GENCC_100002|SFRP4|Pyle disease|Strong|Autosomal recessive|Labcorp Genetics (formerly Invitae)","GENCC_000110-HGNC_10778-ORPHANET_3005-HP_0000007-GENCC_100009|SFRP4|Pyle disease|Supportive|Autosomal recessive|Orphanet","GENCC_000111-HGNC_10778-OMIM_265900-HP_0000007-GENCC_100002|SFRP4|Pyle disease|Strong|Autosomal recessive|PanelApp Australia"]},{"input":"HGNC:17321","source":"HGNC:17321|Sp7 transcription factor","targets":["GENCC_000101-HGNC_17321-OMIM_613849-HP_0000007-GENCC_100004|SP7|osteogenesis imperfecta type 12|Limited|Autosomal recessive|Ambry Genetics","GENCC_000106-HGNC_17321-OMIM_613849-HP_0000007-GENCC_100002|SP7|osteogenesis imperfecta type 12|Strong|Autosomal recessive|Labcorp Genetics (formerly Invitae)","GENCC_000110-HGNC_17321-ORPHANET_216820-HP_0000006-GENCC_100009|SP7|osteogenesis imperfecta type 4|Supportive|Autosomal dominant|Orphanet","GENCC_000111-HGNC_17321-MONDO_0013460-HP_0000007-GENCC_100002|SP7|osteogenesis imperfecta type 12|Strong|Autosomal recessive|PanelApp Australia"]}],"not_found":["HGNC:13361","HGNC:20866"]}