### LOVD-version 3000-210 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = IMMT) # 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}}" "IMMT" "inner membrane protein, mitochondrial" "2" "p11.2" "unknown" "NC_000002.11" "UD_138305911573" "" "" "" "1" "1" "6047" "10989" "600378" "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 15:44:54" "" "" "" "" "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 = 12 "{{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}}" "00002093" "IMMT" "transcript variant X2" "001" "XM_005264108.1" "" "XP_005264165.1" "" "" "" "-759" "2604" "2268" "86423264" "86371055" "00001" "2013-11-15 15:49:01" "" "" "" "2" "00002094" "IMMT" "transcript variant 3" "002" "NM_001100170.1" "" "NP_001093640.1" "" "" "" "-388" "2580" "2244" "86422893" "86371055" "00001" "2013-11-15 15:49:01" "" "" "" "2" "00002095" "IMMT" "transcript variant 2" "003" "NM_001100169.1" "" "NP_001093639.1" "" "" "" "-388" "2610" "2274" "86422893" "86371055" "00001" "2013-11-15 15:49:01" "" "" "" "2" "00002096" "IMMT" "transcript variant 1" "004" "NM_006839.2" "" "NP_006830.2" "" "" "" "-388" "2613" "2277" "86422893" "86371055" "00001" "2013-11-15 15:49:01" "" "" "" "2" "00002097" "IMMT" "transcript variant X5" "005" "XM_005264111.1" "" "XP_005264168.1" "" "" "" "-61" "2577" "2241" "86422566" "86371055" "00001" "2013-11-15 15:49:01" "" "" "" "2" "00002098" "IMMT" "transcript variant X1" "006" "XM_005264107.1" "" "XP_005264164.1" "" "" "" "-60" "2607" "2271" "86422565" "86371055" "00001" "2013-11-15 15:49:01" "" "" "" "2" "00002099" "IMMT" "transcript variant X8" "007" "XM_005264114.1" "" "XP_005264171.1" "" "" "" "-60" "2484" "2148" "86422565" "86371055" "00001" "2013-11-15 15:49:01" "" "" "" "2" "00002100" "IMMT" "transcript variant X4" "008" "XM_005264110.1" "" "XP_005264167.1" "" "" "" "-60" "2577" "2241" "86422565" "86371055" "00001" "2013-11-15 15:49:01" "" "" "" "2" "00002101" "IMMT" "transcript variant X7" "009" "XM_005264113.1" "" "XP_005264170.1" "" "" "" "-56" "2517" "2181" "86422561" "86371055" "00001" "2013-11-15 15:49:01" "" "" "" "2" "00002102" "IMMT" "transcript variant X3" "010" "XM_005264109.1" "" "XP_005264166.1" "" "" "" "-56" "2598" "2262" "86422561" "86371055" "00001" "2013-11-15 15:49:01" "" "" "" "2" "00002103" "IMMT" "transcript variant X9" "011" "XM_005264115.1" "" "XP_005264172.1" "" "" "" "-51" "2472" "2136" "86422556" "86371055" "00001" "2013-11-15 15:49:01" "" "" "" "2" "00002104" "IMMT" "transcript variant X6" "012" "XM_005264112.1" "" "XP_005264169.1" "" "" "" "-33" "2574" "2238" "86422538" "86371055" "00001" "2013-11-15 15:49:01" "" "" "" "2" ## 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