### LOVD-version 3000-210 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = NLRX1) # 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}}" "NLRX1" "NLR family member X1" "11" "q23.3" "unknown" "NC_000011.9" "UD_138455337684" "" "" "" "1" "1" "29890" "79671" "611947" "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 16:06:56" "" "" "" "" "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 = 8 "{{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}}" "00002485" "NLRX1" "transcript variant X1" "001" "XM_005271667.1" "" "XP_005271724.1" "" "" "" "-169" "3505" "2928" "119039036" "119054725" "00001" "2013-11-15 16:09:44" "" "" "" "11" "00002486" "NLRX1" "transcript variant X3" "002" "XM_005271669.1" "" "XP_005271726.1" "" "" "" "-481" "3505" "2928" "119039319" "119054725" "00001" "2013-11-15 16:09:44" "" "" "" "11" "00002487" "NLRX1" "transcript variant X5" "003" "XM_005271671.1" "" "XP_005271728.1" "" "" "" "-842" "2971" "2394" "119039422" "119054725" "00001" "2013-11-15 16:09:44" "" "" "" "11" "00002488" "NLRX1" "transcript variant 1" "004" "NM_024618.2" "" "NP_078894.2" "" "" "" "-239" "3505" "2928" "119039440" "119054725" "00001" "2013-11-15 16:09:44" "" "" "" "11" "00002489" "NLRX1" "transcript variant 2" "005" "NM_170722.1" "" "NP_733840.1" "" "" "" "-239" "2802" "2766" "119039440" "119054725" "00001" "2013-11-15 16:09:44" "" "" "" "11" "00002490" "NLRX1" "transcript variant X6" "006" "XM_005271672.1" "" "XP_005271729.1" "" "" "" "-665" "2971" "2394" "119039451" "119054725" "00001" "2013-11-15 16:09:44" "" "" "" "11" "00002491" "NLRX1" "transcript variant X2" "007" "XM_005271668.1" "" "XP_005271725.1" "" "" "" "-515" "3505" "2928" "119039545" "119054725" "00001" "2013-11-15 16:09:44" "" "" "" "11" "00002492" "NLRX1" "transcript variant X4" "008" "XM_005271670.1" "" "XP_005271727.1" "" "" "" "-668" "2971" "2394" "119039856" "119054725" "00001" "2013-11-15 16:09:44" "" "" "" "11" ## 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