### LOVD-version 3000-210 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = PPOX) # 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}}" "PPOX" "protoporphyrinogen oxidase" "1" "q22" "unknown" "NC_000001.10" "UD_138431484673" "" "" "" "1" "1" "9280" "5498" "600923" "1" "1" "1" "MSeqDR-LSDB" "Variations Associated with Mitochondrial Diseases Gene" "" "" "2" " ; NuclearMitome http://www.transgenomic.com ; 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}}" "00001072" "PPOX" "transcript variant X1" "001" "XM_005245290.1" "" "XP_005245347.1" "" "" "" "-26" "1590" "1548" "161135832" "161141008" "00001" "2013-11-12 21:54:29" "" "" "" "1" "00001073" "PPOX" "transcript variant 2" "002" "NM_001122764.1" "" "NP_001116236.1" "" "" "" "-290" "1478" "1434" "161136181" "161141010" "00001" "2013-11-12 21:54:29" "" "" "" "1" "00001074" "PPOX" "transcript variant 1" "003" "NM_000309.3" "" "NP_000300.1" "" "" "" "-229" "1478" "1434" "161136181" "161141010" "00001" "2013-11-12 21:54:29" "" "" "" "1" "00001075" "PPOX" "transcript variant X2" "004" "XM_005245291.1" "" "XP_005245348.1" "" "" "" "-268" "1506" "1482" "161136203" "161146896" "00001" "2013-11-12 21:54:29" "" "" "" "1" "00001076" "PPOX" "transcript variant X6" "005" "XM_005245295.1" "" "XP_005245352.1" "" "" "" "-524" "1098" "1074" "161136258" "161146896" "00001" "2013-11-12 21:54:29" "" "" "" "1" "00001077" "PPOX" "transcript variant X7" "006" "XM_005245296.1" "" "XP_005245353.1" "" "" "" "-544" "2260" "996" "161136270" "161148136" "00001" "2013-11-12 21:54:29" "" "" "" "1" "00001078" "PPOX" "transcript variant X4" "007" "XM_005245293.1" "" "XP_005245350.1" "" "" "" "-571" "1098" "1074" "161136630" "161146896" "00001" "2013-11-12 21:54:29" "" "" "" "1" "00001079" "PPOX" "transcript variant X5" "008" "XM_005245294.1" "" "XP_005245351.1" "" "" "" "-467" "1098" "1074" "161136630" "161146896" "00001" "2013-11-12 21:54:29" "" "" "" "1" "00001080" "PPOX" "transcript variant X3" "009" "XM_005245292.1" "" "XP_005245349.1" "" "" "" "-8" "1377" "1335" "161136630" "161141008" "00001" "2013-11-12 21:54:29" "" "" "" "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