### LOVD-version 3000-210 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = MOBP) # 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}}" "MOBP" "myelin-associated oligodendrocyte basic protein" "3" "p21.33" "unknown" "NC_000003.11" "UD_138455238316" "" "" "" "1" "1" "7189" "4336" "600948" "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 15:44:54" "" "" "" "" "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 = 10 "{{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}}" "00002217" "MOBP" "transcript variant 6" "001" "NR_103505.1" "" "" "" "" "" "1" "6204" "6204" "39509064" "39570988" "00001" "2013-11-15 15:53:15" "" "" "" "3" "00002218" "MOBP" "transcript variant 5" "002" "NR_103504.1" "" "" "" "" "" "1" "6166" "6166" "39509064" "39570988" "00001" "2013-11-15 15:53:15" "" "" "" "3" "00002219" "MOBP" "transcript variant 4" "003" "NR_003090.2" "" "" "" "" "" "1" "5824" "5824" "39509064" "39570988" "00001" "2013-11-15 15:53:15" "" "" "" "3" "00002220" "MOBP" "transcript variant 1" "004" "NM_001278322.1" "" "NP_001265251.1" "" "" "" "-256" "3241" "621" "39509064" "39557494" "00001" "2013-11-15 15:53:15" "" "" "" "3" "00002221" "MOBP" "transcript variant 3" "005" "NM_182935.3" "" "NP_891980.1" "" "" "" "-256" "2827" "246" "39509064" "39557494" "00001" "2013-11-15 15:53:15" "" "" "" "3" "00002222" "MOBP" "transcript variant 7" "006" "NR_103506.1" "" "" "" "" "" "1" "2873" "2873" "39509064" "39557494" "00001" "2013-11-15 15:53:15" "" "" "" "3" "00002223" "MOBP" "transcript variant X2" "007" "XR_245128.1" "" "" "" "" "" "1" "1642" "1642" "39509075" "39566373" "00001" "2013-11-15 15:53:15" "" "" "" "3" "00002224" "MOBP" "transcript variant X3" "008" "XR_245129.1" "" "" "" "" "" "1" "1623" "1623" "39509096" "39566373" "00001" "2013-11-15 15:53:15" "" "" "" "3" "00002225" "MOBP" "transcript variant X1" "009" "XM_005265167.1" "" "XP_005265224.1" "" "" "" "-82" "699" "552" "39521537" "39544518" "00001" "2013-11-15 15:53:15" "" "" "" "3" "00002226" "MOBP" "transcript variant 2" "010" "NM_001278323.1" "" "NP_001265252.1" "" "" "" "-4" "699" "552" "39543557" "39544518" "00001" "2013-11-15 15:53:15" "" "" "" "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