### LOVD-version 3000-210 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = ANKRD26) # 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}}" "ANKRD26" "ankyrin repeat domain 26" "10" "p12.1" "unknown" "NC_000010.10" "UD_138184185917" "" "" "" "1" "1" "29186" "22852" "610855" "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 15:07:22" "" "" "" "" "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}}" "00001530" "ANKRD26" "transcript variant X2" "001" "XM_005252410.1" "" "XP_005252467.1" "" "" "" "-172" "5022" "5010" "27389427" "27284054" "00001" "2013-11-15 15:08:46" "" "" "" "10" "00001531" "ANKRD26" "transcript variant X1" "002" "XM_005252409.1" "" "XP_005252466.1" "" "" "" "-172" "6670" "5181" "27389427" "27293030" "00001" "2013-11-15 15:08:46" "" "" "" "10" "00001532" "ANKRD26" "transcript variant X5" "003" "XM_005252413.1" "" "XP_005252470.1" "" "" "" "-408" "5779" "4290" "27369882" "27293030" "00001" "2013-11-15 15:08:46" "" "" "" "10" "00001533" "ANKRD26" "transcript variant X7" "004" "XM_005252415.1" "" "XP_005252472.1" "" "" "" "-547" "5236" "3747" "27356116" "27293030" "00001" "2013-11-15 15:08:46" "" "" "" "10" "00001534" "ANKRD26" "transcript variant X4" "005" "XM_005252412.1" "" "XP_005252469.1" "" "" "" "-167" "5980" "4491" "27341147" "27293030" "00001" "2013-11-15 15:08:46" "" "" "" "10" "00001535" "ANKRD26" "transcript variant 2" "006" "NM_001256053.1" "" "NP_001242982.1" "" "" "" "-172" "6604" "5130" "27389427" "27293045" "00001" "2013-11-15 15:08:46" "" "" "" "10" "00001536" "ANKRD26" "transcript variant 1" "007" "NM_014915.2" "" "NP_055730.2" "" "" "" "-172" "6607" "5133" "27389427" "27293045" "00001" "2013-11-15 15:08:46" "" "" "" "10" "00001537" "ANKRD26" "transcript variant X3" "008" "XM_005252411.1" "" "XP_005252468.1" "" "" "" "-172" "4856" "4752" "27389427" "27294567" "00001" "2013-11-15 15:08:46" "" "" "" "10" "00001538" "ANKRD26" "transcript variant X6" "009" "XM_005252414.1" "" "XP_005252471.1" "" "" "" "-172" "4014" "3822" "27389427" "27319319" "00001" "2013-11-15 15:08:46" "" "" "" "10" ## 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