### LOVD-version 3000-210 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = NME6) # 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}}" "NME6" "NME/NM23 nucleoside diphosphate kinase 6" "3" "p21.31" "unknown" "NC_000003.11" "UD_138455343712" "" "" "" "1" "1" "20567" "10201" "608294" "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}}" "00002509" "NME6" "transcript variant X3" "001" "XM_005264791.1" "" "XP_005264848.1" "" "" "" "-410" "1476" "834" "48343719" "48335485" "00001" "2013-11-15 16:10:49" "" "" "" "3" "00002510" "NME6" "transcript variant X2" "002" "XM_005264790.1" "" "XP_005264847.1" "" "" "" "-410" "1637" "966" "48343719" "48335485" "00001" "2013-11-15 16:10:49" "" "" "" "3" "00002511" "NME6" "transcript variant X1" "003" "XM_005264789.1" "" "XP_005264846.1" "" "" "" "-410" "1677" "1035" "48343719" "48335485" "00001" "2013-11-15 16:10:49" "" "" "" "3" "00002512" "NME6" "transcript variant X7" "004" "XR_245088.1" "" "" "" "" "" "1" "2165" "2165" "48343719" "48335485" "00001" "2013-11-15 16:10:49" "" "" "" "3" "00002513" "NME6" "transcript variant X5" "005" "XM_005264793.1" "" "XP_005264850.1" "" "" "" "-56" "1187" "516" "48342858" "48335485" "00001" "2013-11-15 16:10:49" "" "" "" "3" "00002514" "NME6" "transcript variant X4" "006" "XM_005264792.1" "" "XP_005264849.1" "" "" "" "-96" "1203" "561" "48342857" "48335485" "00001" "2013-11-15 16:10:49" "" "" "" "3" "00002515" "NME6" "transcript variant X6" "007" "XM_005264794.1" "" "XP_005264851.1" "" "" "" "-90" "1163" "492" "48342851" "48335485" "00001" "2013-11-15 16:10:49" "" "" "" "3" "00002516" "NME6" "NME/NM23 nucleoside diphosphate kinase 6" "008" "NM_005793.3" "" "NP_005784.1" "" "" "" "-46" "1136" "585" "48342848" "48335576" "00001" "2013-11-15 16:10:49" "" "" "" "3" ## 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