### LOVD-version 3000-210 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = OCIAD1) # 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}}" "OCIAD1" "OCIA domain containing 1" "4" "p11" "unknown" "NC_000004.11" "UD_138455354313" "" "" "" "1" "1" "16074" "54940" "" "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 = 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}}" "00002542" "OCIAD1" "transcript variant X1" "001" "XM_005248112.1" "" "XP_005248169.1" "" "" "" "-97" "1226" "738" "48832599" "48863267" "00001" "2013-11-15 16:12:38" "" "" "" "4" "00002543" "OCIAD1" "transcript variant 4" "002" "NM_001079841.2" "" "NP_001073310.1" "" "" "" "-212" "1685" "564" "48833060" "48863834" "00001" "2013-11-15 16:12:38" "" "" "" "4" "00002544" "OCIAD1" "transcript variant 1" "003" "NM_017830.3" "" "NP_060300.1" "" "" "" "-212" "1793" "738" "48833060" "48863834" "00001" "2013-11-15 16:12:38" "" "" "" "4" "00002545" "OCIAD1" "transcript variant 3" "004" "NM_001079840.2" "" "NP_001073309.1" "" "" "" "-212" "1640" "585" "48833060" "48863834" "00001" "2013-11-15 16:12:38" "" "" "" "4" "00002546" "OCIAD1" "transcript variant X4" "005" "XM_005248115.1" "" "XP_005248172.1" "" "" "" "-203" "911" "423" "48833087" "48863267" "00001" "2013-11-15 16:12:38" "" "" "" "4" "00002547" "OCIAD1" "transcript variant 2" "006" "NM_001079839.2" "" "NP_001073308.1" "" "" "" "-275" "1793" "738" "48833244" "48863834" "00001" "2013-11-15 16:12:38" "" "" "" "4" "00002548" "OCIAD1" "transcript variant 5" "007" "NM_001079842.2" "" "NP_001073311.2" "" "" "" "-275" "1640" "585" "48833244" "48863834" "00001" "2013-11-15 16:12:38" "" "" "" "4" "00002549" "OCIAD1" "transcript variant 6" "008" "NM_001168254.1" "" "NP_001161726.1" "" "" "" "-216" "1808" "753" "48833323" "48863834" "00001" "2013-11-15 16:12:38" "" "" "" "4" "00002550" "OCIAD1" "transcript variant X3" "009" "XM_005248114.1" "" "XP_005248171.1" "" "" "" "-116" "1135" "579" "48833423" "48863269" "00001" "2013-11-15 16:12:38" "" "" "" "4" "00002551" "OCIAD1" "transcript variant X2" "010" "XM_005248113.1" "" "XP_005248170.1" "" "" "" "-116" "1088" "600" "48833423" "48863267" "00001" "2013-11-15 16:12:38" "" "" "" "4" ## 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