### LOVD-version 3000-210 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = NDUFC1) # 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}}" "NDUFC1" "NADH dehydrogenase (ubiquinone) 1, subcomplex unknown, 1, 6kDa" "4" "q31.1" "unknown" "NC_000004.11" "UD_136089523818" "" "" "" "1" "1" "7705" "4717" "603844" "1" "1" "1" "MSeqDR-LSDB" "Variations Associated with Mitochondrial Diseases Gene" "" "" "2" " ; NuclearMitome http://www.transgenomic.com ; MitoCarta http://www.broadinstitute.org/pubs/MitoCarta/ " "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 = 7 "{{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}}" "00000971" "NDUFC1" "transcript variant 6" "001" "NM_001184990.1" "" "NP_001171919.1" "" "" "" "-294" "427" "231" "140223705" "140211071" "00001" "2013-11-12 21:51:35" "" "" "" "4" "00000972" "NDUFC1" "transcript variant 3" "002" "NM_001184987.1" "" "NP_001171916.1" "" "" "" "-298" "427" "231" "140223705" "140211071" "00001" "2013-11-12 21:51:35" "" "" "" "4" "00000973" "NDUFC1" "transcript variant 4" "003" "NM_001184988.1" "" "NP_001171917.1" "" "" "" "-334" "427" "231" "140223705" "140211071" "00001" "2013-11-12 21:51:35" "" "" "" "4" "00000974" "NDUFC1" "transcript variant 5" "004" "NM_001184989.1" "" "NP_001171918.1" "" "" "" "-357" "427" "231" "140223705" "140211071" "00001" "2013-11-12 21:51:35" "" "" "" "4" "00000975" "NDUFC1" "transcript variant 2" "005" "NM_002494.3" "" "NP_002485.1" "" "" "" "-433" "427" "231" "140222388" "140211071" "00001" "2013-11-12 21:51:35" "" "" "" "4" "00000976" "NDUFC1" "transcript variant 7" "006" "NM_001184991.1" "" "NP_001171920.1" "" "" "" "-771" "427" "231" "140222364" "140211071" "00001" "2013-11-12 21:51:35" "" "" "" "4" "00000977" "NDUFC1" "transcript variant 1" "007" "NM_001184986.1" "" "NP_001171915.1" "" "" "" "-830" "427" "231" "140222364" "140211071" "00001" "2013-11-12 21:51:35" "" "" "" "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