### LOVD-version 3000-210 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = OGDH) # 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}}" "OGDH" "oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide)" "7" "p13-p11.2" "unknown" "NC_000007.13" "UD_138312185472" "" "" "" "1" "1" "8124" "4967" "613022" "1" "1" "1" "MSeqDR-LSDB" "Variations Associated with Mitochondrial Diseases Gene" "" "" "2" " ; NuclearMitome http://www.transgenomic.com ; MitoPhenome http://mitophenome.org ; 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 = 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}}" "00001001" "OGDH" "transcript variant X3" "001" "XM_005249761.1" "" "XP_005249818.1" "" "" "" "-176" "4174" "3105" "44646104" "44748667" "00001" "2013-11-12 21:52:23" "" "" "" "7" "00001002" "OGDH" "transcript variant 3" "002" "NM_001165036.1" "" "NP_001158508.1" "" "" "" "-159" "4131" "3060" "44646121" "44748669" "00001" "2013-11-12 21:52:23" "" "" "" "7" "00001003" "OGDH" "transcript variant 1" "003" "NM_002541.3" "" "NP_002532.2" "" "" "" "-159" "4143" "3072" "44646121" "44748669" "00001" "2013-11-12 21:52:23" "" "" "" "7" "00001004" "OGDH" "transcript variant 2" "004" "NM_001003941.2" "" "NP_001003941.1" "" "" "" "-159" "1653" "1284" "44646121" "44716195" "00001" "2013-11-12 21:52:23" "" "" "" "7" "00001005" "OGDH" "transcript variant X4" "005" "XM_005249762.1" "" "XP_005249819.1" "" "" "" "-109" "4174" "3105" "44646167" "44748667" "00001" "2013-11-12 21:52:23" "" "" "" "7" "00001006" "OGDH" "transcript variant X5" "006" "XM_005249763.1" "" "XP_005249820.1" "" "" "" "-109" "3691" "2622" "44646171" "44748667" "00001" "2013-11-12 21:52:23" "" "" "" "7" "00001007" "OGDH" "transcript variant X1" "007" "XM_005249759.1" "" "XP_005249816.1" "" "" "" "-91" "4186" "3117" "44646189" "44748667" "00001" "2013-11-12 21:52:23" "" "" "" "7" "00001008" "OGDH" "transcript variant X2" "008" "XM_005249760.1" "" "XP_005249817.1" "" "" "" "-50" "4186" "3117" "44646226" "44748667" "00001" "2013-11-12 21:52:23" "" "" "" "7" ## 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