### LOVD-version 3000-210 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = MECR) # 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}}" "MECR" "mitochondrial trans-2-enoyl-CoA reductase" "1" "p35.3" "unknown" "NC_000001.10" "UD_138455234440" "" "" "" "1" "1" "19691" "51102" "608205" "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 = 8 "{{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}}" "00002207" "MECR" "transcript variant 1" "001" "NM_016011.2" "" "NP_057095.2" "" "" "" "-36" "2271" "1122" "29557454" "29519385" "00001" "2013-11-15 15:52:37" "" "" "" "1" "00002208" "MECR" "transcript variant 2" "002" "NM_001024732.1" "" "NP_001019903.1" "" "" "" "-391" "2043" "894" "29557454" "29519385" "00001" "2013-11-15 15:52:37" "" "" "" "1" "00002209" "MECR" "transcript variant X2" "003" "XM_005245886.1" "" "XP_005245943.1" "" "" "" "-475" "1099" "894" "29557460" "29520329" "00001" "2013-11-15 15:52:37" "" "" "" "1" "00002210" "MECR" "transcript variant X3" "004" "XM_005245887.1" "" "XP_005245944.1" "" "" "" "-599" "1099" "894" "29557457" "29520329" "00001" "2013-11-15 15:52:37" "" "" "" "1" "00002211" "MECR" "transcript variant X5" "005" "XM_005245889.1" "" "XP_005245946.1" "" "" "" "-603" "1099" "894" "29557457" "29520329" "00001" "2013-11-15 15:52:37" "" "" "" "1" "00002212" "MECR" "transcript variant X1" "006" "XM_005245885.1" "" "XP_005245942.1" "" "" "" "-18" "1411" "1206" "29557436" "29520329" "00001" "2013-11-15 15:52:37" "" "" "" "1" "00002213" "MECR" "transcript variant X4" "007" "XM_005245888.1" "" "XP_005245945.1" "" "" "" "-439" "1099" "894" "29557418" "29520329" "00001" "2013-11-15 15:52:37" "" "" "" "1" "00002214" "MECR" "transcript variant X6" "008" "XM_005245890.1" "" "XP_005245947.1" "" "" "" "-41" "834" "834" "29557459" "29527024" "00001" "2013-11-15 15:52:37" "" "" "" "1" ## 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