### LOVD-version 3000-210 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = OGG1) # charset = UTF-8 ## Genes ## Do not remove or alter this header ## ## Count = 1 "{{id}}" "{{name}}" "{{chromosome}}" "{{chrom_band}}" "{{imprinting}}" "{{refseq_genomic}}" "{{refseq_UD}}" "{{reference}}" "{{url_homepage}}" "{{url_external}}" "{{allow_download}}" "{{allow_index_wiki}}" "{{id_hgnc}}" "{{id_entrez}}" "{{id_omim}}" "{{show_hgmd}}" "{{show_genecards}}" "{{show_genetests}}" "{{note_index}}" "{{note_listing}}" "{{refseq}}" "{{refseq_url}}" "{{disclaimer}}" "{{disclaimer_text}}" "{{header}}" "{{header_align}}" "{{footer}}" "{{footer_align}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "{{updated_by}}" "{{updated_date}}" "{{iNote}}" "OGG1" "8-oxoguanine DNA glycosylase" "3" "p26" "unknown" "NC_000003.11" "UD_138312189216" "" "" "" "1" "1" "8125" "4968" "601982" "1" "1" "1" "MSeqDR-LSDB" "Variations Associated with Mitochondrial Diseases Gene" "" "" "2" " ; MitoPhenome http://mitophenome.org ; MitoCarta http://www.broadinstitute.org/pubs/MitoCarta/ " "MSeqDR-LSDB: Mitochondrial Disease LSDB" "-1" "Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium" "-1" "00001" "2013-11-12 21:46:20" "" "" "" "" "The gene panel from GenDX, MitoPhenome, and NuclearMitome, and MitoCarta, plus all genes on chromosome M" ## Transcripts ## Do not remove or alter this header ## ## Count = 9 "{{id}}" "{{geneid}}" "{{name}}" "{{id_mutalyzer}}" "{{id_ncbi}}" "{{id_ensembl}}" "{{id_protein_ncbi}}" "{{id_protein_ensembl}}" "{{id_protein_uniprot}}" "{{remarks}}" "{{position_c_mrna_start}}" "{{position_c_mrna_end}}" "{{position_c_cds_end}}" "{{position_g_mrna_start}}" "{{position_g_mrna_end}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "{{iNote}}" "{{chrom}}" "00001009" "OGG1" "transcript variant 2d" "001" "NM_016828.2" "" "NP_058437.1" "" "" "" "-343" "1909" "1071" "9791628" "9808353" "00001" "2013-11-12 21:52:26" "" "" "" "3" "00001010" "OGG1" "transcript variant 2e" "002" "NM_016829.2" "" "NP_058438.1" "" "" "" "-343" "1862" "969" "9791628" "9808353" "00001" "2013-11-12 21:52:26" "" "" "" "3" "00001011" "OGG1" "transcript variant 2a" "003" "NM_016821.2" "" "NP_058214.1" "" "" "" "-343" "1809" "1275" "9791628" "9808353" "00001" "2013-11-12 21:52:26" "" "" "" "3" "00001012" "OGG1" "transcript variant 2b" "004" "NM_016826.2" "" "NP_058434.1" "" "" "" "-343" "1608" "1074" "9791628" "9808353" "00001" "2013-11-12 21:52:26" "" "" "" "3" "00001013" "OGG1" "transcript variant 2c" "005" "NM_016827.2" "" "NP_058436.1" "" "" "" "-343" "1426" "588" "9791628" "9808353" "00001" "2013-11-12 21:52:26" "" "" "" "3" "00001014" "OGG1" "transcript variant 1b" "006" "NM_016819.3" "" "NP_058212.1" "" "" "" "-343" "1539" "975" "9791628" "9799091" "00001" "2013-11-12 21:52:26" "" "" "" "3" "00001015" "OGG1" "transcript variant 1c" "007" "NM_016820.3" "" "NP_058213.1" "" "" "" "-343" "1312" "1233" "9791628" "9799091" "00001" "2013-11-12 21:52:26" "" "" "" "3" "00001016" "OGG1" "transcript variant 1a" "008" "NM_002542.5" "" "NP_002533.1" "" "" "" "-343" "1295" "1038" "9791628" "9799091" "00001" "2013-11-12 21:52:26" "" "" "" "3" "00001017" "OGG1" "transcript variant X1" "009" "XM_005265185.1" "" "XP_005265242.1" "" "" "" "-341" "1005" "960" "9791630" "9829468" "00001" "2013-11-12 21:52:26" "" "" "" "3" ## Diseases ## Do not remove or alter this header ## ## Count = 0 ## Genes_To_Diseases ## Do not remove or alter this header ## ## Count = 0 ## Individuals ## Do not remove or alter this header ## ## Count = 0 ## Individuals_To_Diseases ## Do not remove or alter this header ## ## Count = 0 ## Phenotypes ## Do not remove or alter this header ## ## Count = 0 ## Screenings ## Do not remove or alter this header ## ## Count = 0 ## Screenings_To_Genes ## Do not remove or alter this header ## ## Count = 0 ## Variants_On_Genome ## Do not remove or alter this header ## ## Please note that not necessarily all variants found in the given individuals are shown. This output is restricted to variants in the selected gene. ## Count = 0 ## Variants_On_Transcripts ## Do not remove or alter this header ## ## Please note that not necessarily all variants found in the given individuals are shown. This output is restricted to variants in the selected gene. ## Count = 0 ## Screenings_To_Variants ## Do not remove or alter this header ## ## Count = 0