### LOVD-version 3000-210 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = MAPT) # 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}}" "MAPT" "microtubule-associated protein tau" "17" "q21" "unknown" "NC_000017.10" "UD_138306357442" "" "" "" "1" "1" "6893" "4137" "157140" "1" "1" "1" "MSeqDR-LSDB" "Variations Associated with Mitochondrial Diseases Gene" "" "" "2" " ; NuclearMitome http://www.transgenomic.com " "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 = 19 "{{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}}" "00000858" "MAPT" "transcript variant X10" "001" "XM_005257371.1" "" "XP_005257428.1" "" "" "" "-368" "1625" "1350" "43971702" "44101812" "00001" "2013-11-12 21:47:13" "" "" "" "17" "00000859" "MAPT" "transcript variant 6" "002" "NM_001123066.3" "" "NP_001116538.2" "" "" "" "-322" "6494" "2331" "43971748" "44105700" "00001" "2013-11-12 21:47:13" "" "" "" "17" "00000860" "MAPT" "transcript variant 1" "003" "NM_016835.4" "" "NP_058519.3" "" "" "" "-322" "6440" "2277" "43971748" "44105700" "00001" "2013-11-12 21:47:13" "" "" "" "17" "00000861" "MAPT" "transcript variant 2" "004" "NM_005910.5" "" "NP_005901.2" "" "" "" "-322" "5489" "1326" "43971748" "44105700" "00001" "2013-11-12 21:47:13" "" "" "" "17" "00000862" "MAPT" "transcript variant 8" "005" "NM_001203252.1" "" "NP_001190181.1" "" "" "" "-322" "5396" "1233" "43971748" "44105700" "00001" "2013-11-12 21:47:13" "" "" "" "17" "00000863" "MAPT" "transcript variant 5" "006" "NM_001123067.3" "" "NP_001116539.1" "" "" "" "-322" "5402" "1239" "43971748" "44105700" "00001" "2013-11-12 21:47:13" "" "" "" "17" "00000864" "MAPT" "transcript variant 7" "007" "NM_001203251.1" "" "NP_001190180.1" "" "" "" "-322" "5309" "1146" "43971748" "44105700" "00001" "2013-11-12 21:47:13" "" "" "" "17" "00000865" "MAPT" "transcript variant 3" "008" "NM_016834.4" "" "NP_058518.1" "" "" "" "-322" "5315" "1152" "43971748" "44105700" "00001" "2013-11-12 21:47:13" "" "" "" "17" "00000866" "MAPT" "transcript variant 4" "009" "NM_016841.4" "" "NP_058525.1" "" "" "" "-322" "5222" "1059" "43971748" "44105700" "00001" "2013-11-12 21:47:13" "" "" "" "17" "00000867" "MAPT" "transcript variant X1" "010" "XM_005257362.1" "" "XP_005257419.1" "" "" "" "-178" "2864" "2589" "43971892" "44101812" "00001" "2013-11-12 21:47:13" "" "" "" "17" "00000868" "MAPT" "transcript variant X4" "011" "XM_005257365.1" "" "XP_005257422.1" "" "" "" "-178" "2771" "2496" "43971892" "44101812" "00001" "2013-11-12 21:47:13" "" "" "" "17" "00000869" "MAPT" "transcript variant X6" "012" "XM_005257367.1" "" "XP_005257424.1" "" "" "" "-178" "2666" "2391" "43971892" "44101812" "00001" "2013-11-12 21:47:13" "" "" "" "17" "00000870" "MAPT" "transcript variant X7" "013" "XM_005257368.1" "" "XP_005257425.1" "" "" "" "-178" "2573" "2298" "43971892" "44101812" "00001" "2013-11-12 21:47:13" "" "" "" "17" "00000871" "MAPT" "transcript variant X3" "014" "XM_005257364.1" "" "XP_005257421.1" "" "" "" "-178" "2777" "2502" "43971892" "44101812" "00001" "2013-11-12 21:47:13" "" "" "" "17" "00000872" "MAPT" "transcript variant X8" "015" "XM_005257369.1" "" "XP_005257426.1" "" "" "" "-177" "1799" "1524" "43971893" "44101812" "00001" "2013-11-12 21:47:13" "" "" "" "17" "00000873" "MAPT" "transcript variant X9" "016" "XM_005257370.1" "" "XP_005257427.1" "" "" "" "-176" "1712" "1437" "43971894" "44101812" "00001" "2013-11-12 21:47:13" "" "" "" "17" "00000874" "MAPT" "transcript variant X5" "017" "XM_005257366.1" "" "XP_005257423.1" "" "" "" "-144" "2690" "2415" "43971926" "44101812" "00001" "2013-11-12 21:47:13" "" "" "" "17" "00000875" "MAPT" "transcript variant X2" "018" "XM_005257363.1" "" "XP_005257420.1" "" "" "" "-92" "2864" "2589" "44039049" "44101812" "00001" "2013-11-12 21:47:13" "" "" "" "17" "00000876" "MAPT" "transcript variant X11" "019" "XM_005257372.1" "" "XP_005257429.1" "" "" "" "-76" "1448" "1173" "44063013" "44101812" "00001" "2013-11-12 21:47:13" "" "" "" "17" ## 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