### LOVD-version 3000-210 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = SLC19A3) # 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}}" "SLC19A3" "solute carrier family 19 (thiamine transporter), member 3" "2" "q37" "unknown" "NC_000002.11" "UD_138385436661" "" "" "" "1" "1" "16266" "80704" "606152" "1" "1" "1" "MSeqDR-LSDB" "Variations Associated with Mitochondrial Diseases Gene" "" "" "2" "Sources: GeneDX http://www.genedx.com" "MSeqDR-LSDB: Mitochondrial Disease LSDB" "0" "Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium" "0" "00001" "2013-11-07 13:50:45" "" "" "" "" "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}}" "00000296" "SLC19A3" "transcript variant X1" "001" "XM_005246871.1" "" "XP_005246928.1" "" "" "" "-8" "3828" "1641" "228582814" "228549926" "00001" "2013-11-07 13:59:37" "" "" "" "2" "00000297" "SLC19A3" "solute carrier family 19 (thiamine transporter), member 3" "002" "NM_025243.3" "" "NP_079519.1" "" "" "" "-89" "3678" "1491" "228582745" "228549926" "00001" "2013-11-07 13:59:37" "" "" "" "2" "00000298" "SLC19A3" "transcript variant X4" "003" "XM_005246874.1" "" "XP_005246931.1" "" "" "" "-267" "3021" "1479" "228582715" "228550571" "00001" "2013-11-07 13:59:37" "" "" "" "2" "00000299" "SLC19A3" "transcript variant X3" "004" "XM_005246873.1" "" "XP_005246930.1" "" "" "" "-166" "3033" "1491" "228579328" "228550571" "00001" "2013-11-07 13:59:37" "" "" "" "2" "00000300" "SLC19A3" "transcript variant X2" "005" "XM_005246872.1" "" "XP_005246929.1" "" "" "" "-163" "3069" "1527" "228571227" "228550571" "00001" "2013-11-07 13:59:37" "" "" "" "2" "00000301" "SLC19A3" "transcript variant X5" "006" "XM_005246875.1" "" "XP_005246932.1" "" "" "" "-8" "1249" "1152" "228582814" "228552904" "00001" "2013-11-07 13:59:37" "" "" "" "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