### LOVD-version 3000-210 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = KIAA0141) # 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}}" "KIAA0141" "KIAA0141" "5" "q31" "unknown" "NC_000005.9" "UD_138306053936" "" "" "" "1" "1" "28969" "9812" "" "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 = 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}}" "00002117" "KIAA0141" "transcript variant X4" "001" "XM_005268550.1" "" "XP_005268607.1" "" "" "" "-157" "1568" "1194" "141303350" "141330027" "00001" "2013-11-15 15:49:18" "" "" "" "5" "00002118" "KIAA0141" "transcript variant X3" "002" "XM_005268549.1" "" "XP_005268606.1" "" "" "" "-157" "1629" "1548" "141303350" "141328976" "00001" "2013-11-15 15:49:18" "" "" "" "5" "00002119" "KIAA0141" "transcript variant X1" "003" "XM_005268547.1" "" "XP_005268604.1" "" "" "" "-157" "4743" "1548" "141303350" "141321610" "00001" "2013-11-15 15:49:18" "" "" "" "5" "00002120" "KIAA0141" "transcript variant X7" "004" "XR_245861.1" "" "" "" "" "" "1" "4299" "4299" "141303350" "141321610" "00001" "2013-11-15 15:49:18" "" "" "" "5" "00002121" "KIAA0141" "transcript variant X2" "005" "XM_005268548.1" "" "XP_005268605.1" "" "" "" "-157" "4089" "1548" "141303350" "141321610" "00001" "2013-11-15 15:49:18" "" "" "" "5" "00002122" "KIAA0141" "transcript variant X6" "006" "XM_005268552.1" "" "XP_005268609.1" "" "" "" "-157" "1369" "1170" "141303350" "141318305" "00001" "2013-11-15 15:49:18" "" "" "" "5" "00002123" "KIAA0141" "transcript variant X5" "007" "XM_005268551.1" "" "XP_005268608.1" "" "" "" "-157" "1487" "1185" "141303350" "141316756" "00001" "2013-11-15 15:49:18" "" "" "" "5" "00002124" "KIAA0141" "transcript variant 1" "008" "NM_014773.3" "" "NP_055588.3" "" "" "" "-122" "4836" "1548" "141303385" "141321612" "00001" "2013-11-15 15:49:18" "" "" "" "5" "00002125" "KIAA0141" "transcript variant 2" "009" "NM_001142603.1" "" "NP_001136075.1" "" "" "" "-122" "4043" "1548" "141303385" "141321612" "00001" "2013-11-15 15:49:19" "" "" "" "5" ## 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