### LOVD-version 3000-210 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = TPM2) # 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}}" "TPM2" "tropomyosin 2 (beta)" "9" "p13" "unknown" "NC_000009.11" "UD_138314076435" "" "" "" "1" "1" "12011" "7169" "190990" "1" "1" "1" "MSeqDR-LSDB" "Variations Associated with Mitochondrial Diseases Gene" "" "" "2" " ; NuclearMitome http://www.transgenomic.com " "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 = 10 "{{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}}" "00001240" "TPM2" "transcript variant 2" "001" "NM_213674.1" "" "NP_998839.1" "" "" "" "-239" "943" "855" "35690053" "35681990" "00001" "2013-11-12 21:58:54" "" "" "" "9" "00001241" "TPM2" "transcript variant X1" "002" "XM_005251565.1" "" "XP_005251622.1" "" "" "" "-769" "1027" "954" "35690583" "35682005" "00001" "2013-11-12 21:58:54" "" "" "" "9" "00001242" "TPM2" "transcript variant X6" "003" "XM_005251570.1" "" "XP_005251627.1" "" "" "" "-111" "928" "855" "35689925" "35682005" "00001" "2013-11-12 21:58:54" "" "" "" "9" "00001243" "TPM2" "transcript variant X4" "004" "XM_005251568.1" "" "XP_005251625.1" "" "" "" "-111" "1646" "855" "35689925" "35682005" "00001" "2013-11-12 21:58:54" "" "" "" "9" "00001244" "TPM2" "transcript variant X5" "005" "XM_005251569.1" "" "XP_005251626.1" "" "" "" "-111" "1646" "855" "35689925" "35682005" "00001" "2013-11-12 21:58:54" "" "" "" "9" "00001245" "TPM2" "transcript variant X8" "006" "XM_005251572.1" "" "XP_005251629.1" "" "" "" "-111" "1004" "642" "35689925" "35682005" "00001" "2013-11-12 21:58:54" "" "" "" "9" "00001246" "TPM2" "transcript variant X7" "007" "XM_005251571.1" "" "XP_005251628.1" "" "" "" "-111" "1722" "642" "35689925" "35682005" "00001" "2013-11-12 21:58:54" "" "" "" "9" "00001247" "TPM2" "transcript variant X3" "008" "XM_005251567.1" "" "XP_005251624.1" "" "" "" "-111" "1260" "912" "35689925" "35682005" "00001" "2013-11-12 21:58:54" "" "" "" "9" "00001248" "TPM2" "transcript variant X2" "009" "XM_005251566.1" "" "XP_005251623.1" "" "" "" "-111" "1978" "912" "35689925" "35682005" "00001" "2013-11-12 21:58:54" "" "" "" "9" "00001249" "TPM2" "transcript variant 1" "010" "NM_003289.3" "" "NP_003280.2" "" "" "" "-239" "1088" "855" "35690053" "35682923" "00001" "2013-11-12 21:58:54" "" "" "" "9" ## 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