### LOVD-version 3000-210 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = MFSD8) # 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}}" "MFSD8" "major facilitator superfamily domain containing 8" "4" "q28.2" "unknown" "NC_000004.11" "UD_138394113312" "" "" "" "1" "1" "28486" "256471" "611124" "1" "1" "1" "MSeqDR-LSDB" "Variations Associated with Mitochondrial Diseases Gene" "" "" "2" " ; NuclearMitome http://www.transgenomic.com " "MSeqDR-LSDB: Mitochondrial Disease LSDB" "-1" "Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium" "-1" "00001" "2013-11-12 21:46:20" "" "" "" "" "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 = 9 "{{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}}" "00003384" "MFSD8" "major facilitator superfamily domain containing 8" "002" "NM_152778.2" "" "NP_689991.1" "" "" "" "-163" "4382" "1557" "128887139" "128838960" "00001" "2015-01-22 14:00:15" "" "" "" "" "00003385" "MFSD8" "transcript variant X1" "006" "XM_005262893.1" "" "XP_005262950.1" "" "" "" "-77" "4382" "1557" "128886365" "128838960" "00001" "2015-01-22 14:00:15" "" "" "" "" "00003386" "MFSD8" "transcript variant X2" "003" "XM_005262894.1" "" "XP_005262951.1" "" "" "" "-77" "4268" "1443" "128886365" "128838960" "00001" "2015-01-22 14:00:15" "" "" "" "" "00003387" "MFSD8" "transcript variant X3" "001" "XM_005262895.1" "" "XP_005262952.1" "" "" "" "-207" "4247" "1422" "128887185" "128838960" "00001" "2015-01-22 14:00:15" "" "" "" "" "00003388" "MFSD8" "transcript variant X4" "005" "XM_005262896.1" "" "XP_005262953.1" "" "" "" "-77" "4235" "1410" "128886365" "128838960" "00001" "2015-01-22 14:00:15" "" "" "" "" "00003389" "MFSD8" "transcript variant X5" "004" "XM_005262897.1" "" "XP_005262954.1" "" "" "" "-77" "4181" "1356" "128886365" "128838960" "00001" "2015-01-22 14:00:15" "" "" "" "" "00003390" "MFSD8" "transcript variant X6" "008" "XM_005262898.1" "" "XP_005262955.1" "" "" "" "-77" "1301" "1011" "128886365" "128842624" "00001" "2015-01-22 14:00:15" "" "" "" "" "00003391" "MFSD8" "transcript variant X7" "007" "XM_005262899.1" "" "XP_005262956.1" "" "" "" "-77" "1187" "897" "128886365" "128842624" "00001" "2015-01-22 14:00:15" "" "" "" "" "00003392" "MFSD8" "transcript variant X8" "009" "XM_005262900.1" "" "XP_005262957.1" "" "" "" "-77" "794" "690" "128886365" "128851897" "00001" "2015-01-22 14:00:15" "" "" "" "" ## 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