### LOVD-version 3000-210 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = NUDT13) # 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}}" "NUDT13" "nudix (nucleoside diphosphate linked moiety X)-type motif 13" "10" "q22.3" "unknown" "NC_000010.10" "UD_138306845271" "" "" "" "1" "1" "18827" "25961" "609233" "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 = 6 "{{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}}" "00002528" "NUDT13" "transcript variant X5" "001" "XR_246082.1" "" "" "" "" "" "1" "2221" "2221" "74870133" "74891583" "00001" "2013-11-15 16:11:54" "" "" "" "10" "00002529" "NUDT13" "transcript variant X2" "002" "XM_005269682.1" "" "XP_005269739.1" "" "" "" "-202" "1869" "708" "74870133" "74891583" "00001" "2013-11-15 16:11:54" "" "" "" "10" "00002530" "NUDT13" "transcript variant X1" "003" "XM_005269681.1" "" "XP_005269738.1" "" "" "" "-202" "1714" "792" "74870133" "74891583" "00001" "2013-11-15 16:11:54" "" "" "" "10" "00002531" "NUDT13" "transcript variant X4" "004" "XM_005269684.1" "" "XP_005269741.1" "" "" "" "-202" "703" "609" "74870133" "74886504" "00001" "2013-11-15 16:11:54" "" "" "" "10" "00002532" "NUDT13" "nudix (nucleoside diphosphate linked moiety X)-type motif 13" "005" "NM_015901.4" "" "NP_056985.3" "" "" "" "-125" "1979" "1059" "74870210" "74891581" "00001" "2013-11-15 16:11:54" "" "" "" "10" "00002533" "NUDT13" "transcript variant X3" "006" "XM_005269683.1" "" "XP_005269740.1" "" "" "" "-505" "1603" "681" "74870280" "74891583" "00001" "2013-11-15 16:11:54" "" "" "" "10" ## 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