{"count":3,"next":null,"previous":null,"results":[{"gene_data":{"alias":["MCP1","MCP-1","MCAF","SMC-CF","GDCF-2","HC11","MGC9434"],"biotype":"protein_coding","hgnc_id":"HGNC:10618","gene_name":"C-C motif chemokine ligand 2","omim_gene":["158105"],"alias_name":["monocyte chemotactic protein 1, homologous to mouse Sig-je","monocyte chemoattractant protein-1","monocyte chemotactic and activating factor","monocyte secretory protein JE","small inducible cytokine subfamily A (Cys-Cys), member 2"],"gene_symbol":"CCL2","hgnc_symbol":"CCL2","hgnc_release":"2017-11-03T00:00:00","ensembl_genes":{"GRch37":{"82":{"location":"17:32582304-32584222","ensembl_id":"ENSG00000108691"}},"GRch38":{"90":{"location":"17:34255218-34257203","ensembl_id":"ENSG00000108691"}}},"hgnc_date_symbol_changed":"2002-08-23"},"entity_type":"gene","entity_name":"CCL2","confidence_level":"1","penetrance":"Complete","mode_of_pathogenicity":"","publications":[],"evidence":["Radboud University Medical Center, Nijmegen"],"phenotypes":["Susceptibility to spina bifida"],"mode_of_inheritance":"","tags":[],"panel":{"id":11,"hash_id":"57e3df7e8f62034b82c0d332","name":"Familial Neural Tube Defects","disease_group":"","disease_sub_group":"","status":"public","version":"1.5","version_created":"2017-11-05T02:37:19.836037Z","relevant_disorders":[],"stats":{"number_of_genes":44,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["MCP1","MCP-1","MCAF","SMC-CF","GDCF-2","HC11","MGC9434"],"biotype":"protein_coding","hgnc_id":"HGNC:10618","gene_name":"C-C motif chemokine ligand 2","omim_gene":["158105"],"alias_name":["monocyte chemotactic protein 1, homologous to mouse Sig-je","monocyte chemoattractant protein-1","monocyte chemotactic and activating factor","monocyte secretory protein JE","small inducible cytokine subfamily A (Cys-Cys), member 2"],"gene_symbol":"CCL2","hgnc_symbol":"CCL2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"17:32582304-32584222","ensembl_id":"ENSG00000108691"}},"GRch38":{"90":{"location":"17:34255218-34257203","ensembl_id":"ENSG00000108691"}}},"hgnc_date_symbol_changed":"2002-08-23"},"entity_type":"gene","entity_name":"CCL2","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":null,"publications":["28787010"],"evidence":["Literature"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":394,"hash_id":null,"name":"Familial Meniere Disease","disease_group":"Hearing and ear disorders","disease_sub_group":"Other hearing and ear disorders","status":"public","version":"1.1","version_created":"2018-01-17T16:26:29.432517Z","relevant_disorders":[],"stats":{"number_of_genes":130,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"}]}},{"gene_data":{"alias":["MCP1","MCP-1","MCAF","SMC-CF","GDCF-2","HC11","MGC9434"],"biotype":"protein_coding","hgnc_id":"HGNC:10618","gene_name":"C-C motif chemokine ligand 2","omim_gene":["158105"],"alias_name":["monocyte chemotactic protein 1, homologous to mouse Sig-je","monocyte chemoattractant protein-1","monocyte chemotactic and activating factor","monocyte secretory protein JE","small inducible cytokine subfamily A (Cys-Cys), member 2"],"gene_symbol":"CCL2","hgnc_symbol":"CCL2","hgnc_release":"2017-11-03","ensembl_genes":{"GRch37":{"82":{"location":"17:32582304-32584222","ensembl_id":"ENSG00000108691"}},"GRch38":{"90":{"location":"17:34255218-34257203","ensembl_id":"ENSG00000108691"}}},"hgnc_date_symbol_changed":"2002-08-23"},"entity_type":"gene","entity_name":"CCL2","confidence_level":"1","penetrance":null,"mode_of_pathogenicity":null,"publications":["25499426","22248664","23449669","21345872"],"evidence":["EUROPAC"],"phenotypes":[],"mode_of_inheritance":"","tags":[],"panel":{"id":386,"hash_id":null,"name":"Pancreatitis","disease_group":"","disease_sub_group":"","status":"public","version":"2.0","version_created":"2019-09-04T09:45:14.660178Z","relevant_disorders":["R175"],"stats":{"number_of_genes":16,"number_of_strs":0,"number_of_regions":0},"types":[{"name":"Rare Disease 100K","slug":"rare-disease-100k","description":"Rare Disease 100K"},{"name":"GMS Rare Disease","slug":"gms-rare-disease","description":"This panel type is used for GMS panels that are not virtual (i.e. could be a wet lab test)"},{"name":"GMS signed-off","slug":"gms-signed-off","description":"This panel has undergone review by a NHSE GMS disease specialist group and processes to be signed-off for use within the GMS."}]}}]}