### LOVD-version 3000-210 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = DAP3) # 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}}" "DAP3" "death associated protein 3" "1" "q22" "unknown" "NC_000001.10" "UD_138304818752" "" "" "" "1" "1" "2673" "7818" "602074" "1" "1" "1" "MSeqDR-LSDB" "Variations Associated with Mitochondrial Diseases Gene" "" "" "2" " ; MitoCarta http://www.broadinstitute.org/pubs/MitoCarta/ " "MSeqDR-LSDB: Mitochondrial Disease LSDB" "-1" "Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium" "-1" "00001" "2013-11-15 15:07:22" "" "" "" "" "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}}" "00001800" "DAP3" "transcript variant X1" "001" "XM_005245479.1" "" "XP_005245536.1" "" "" "" "-378" "1484" "1197" "155657693" "155708320" "00001" "2013-11-15 15:18:28" "" "" "" "1" "00001801" "DAP3" "transcript variant X3" "002" "XM_005245481.1" "" "XP_005245538.1" "" "" "" "-189" "1361" "1074" "155658853" "155708320" "00001" "2013-11-15 15:18:28" "" "" "" "1" "00001802" "DAP3" "transcript variant X2" "003" "XM_005245480.1" "" "XP_005245537.1" "" "" "" "-168" "1382" "1095" "155658874" "155708320" "00001" "2013-11-15 15:18:28" "" "" "" "1" "00001803" "DAP3" "transcript variant X4" "004" "XM_005245482.1" "" "XP_005245539.1" "" "" "" "-92" "1259" "972" "155658881" "155708320" "00001" "2013-11-15 15:18:28" "" "" "" "1" "00001804" "DAP3" "transcript variant 3" "005" "NM_001199849.1" "" "NP_001186778.1" "" "" "" "-184" "1965" "1197" "155658882" "155708801" "00001" "2013-11-15 15:18:28" "" "" "" "1" "00001805" "DAP3" "transcript variant 4" "006" "NM_001199850.1" "" "NP_001186779.1" "" "" "" "-91" "1863" "1095" "155658882" "155708801" "00001" "2013-11-15 15:18:28" "" "" "" "1" "00001806" "DAP3" "transcript variant 5" "007" "NM_001199851.1" "" "NP_001186780.1" "" "" "" "-91" "1842" "1074" "155658882" "155708801" "00001" "2013-11-15 15:18:28" "" "" "" "1" "00001807" "DAP3" "transcript variant 1" "008" "NM_033657.2" "" "NP_387506.1" "" "" "" "-157" "1965" "1197" "155658885" "155708801" "00001" "2013-11-15 15:18:28" "" "" "" "1" "00001808" "DAP3" "transcript variant 2" "009" "NM_004632.3" "" "NP_004623.1" "" "" "" "-88" "1965" "1197" "155658885" "155708801" "00001" "2013-11-15 15:18:28" "" "" "" "1" ## 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