### LOVD-version 3000-210 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = SLC25A30) # 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}}" "SLC25A30" "solute carrier family 25, member 30" "13" "q14" "unknown" "NC_000013.10" "UD_138313424455" "" "" "" "1" "1" "27371" "253512" "610793" "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}}" "00002898" "SLC25A30" "transcript variant X3" "001" "XM_005266323.1" "" "XP_005266380.1" "" "" "" "-137" "893" "765" "45992516" "45960520" "00001" "2013-11-15 16:25:13" "" "" "" "13" "00002899" "SLC25A30" "transcript variant X4" "002" "XM_005266324.1" "" "XP_005266381.1" "" "" "" "-204" "3381" "723" "45992549" "45967451" "00001" "2013-11-15 16:25:13" "" "" "" "13" "00002900" "SLC25A30" "solute carrier family 25, member 30" "003" "NM_001010875.2" "" "NP_001010875.1" "" "" "" "-137" "3534" "876" "45992516" "45967451" "00001" "2013-11-15 16:25:13" "" "" "" "13" "00002901" "SLC25A30" "transcript variant X5" "004" "XM_005266325.1" "" "XP_005266382.1" "" "" "" "-213" "3309" "651" "45992515" "45967451" "00001" "2013-11-15 16:25:13" "" "" "" "13" "00002902" "SLC25A30" "transcript variant X6" "005" "XM_005266326.1" "" "XP_005266383.1" "" "" "" "-338" "3309" "651" "45986073" "45967451" "00001" "2013-11-15 16:25:13" "" "" "" "13" "00002903" "SLC25A30" "transcript variant X1" "006" "XM_005266321.1" "" "XP_005266378.1" "" "" "" "-137" "1050" "882" "45992516" "45970157" "00001" "2013-11-15 16:25:13" "" "" "" "13" "00002904" "SLC25A30" "transcript variant X7" "007" "XM_005266327.1" "" "XP_005266384.1" "" "" "" "-54" "684" "516" "45976973" "45970157" "00001" "2013-11-15 16:25:13" "" "" "" "13" "00002905" "SLC25A30" "transcript variant X2" "008" "XM_005266322.1" "" "XP_005266379.1" "" "" "" "-137" "931" "765" "45992516" "45972022" "00001" "2013-11-15 16:25:13" "" "" "" "13" ## 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