### LOVD-version 3000-210 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = TDRKH) # 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}}" "TDRKH" "tudor and KH domain containing" "1" "q21" "unknown" "NC_000001.10" "UD_138313853492" "" "" "" "1" "1" "11713" "11022" "609501" "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 16:06:56" "" "" "" "" "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}}" "00002988" "TDRKH" "transcript variant X1" "001" "XM_005244853.1" "" "XP_005244910.1" "" "" "" "-224" "2023" "1686" "151763052" "151742741" "00001" "2013-11-15 16:28:31" "" "" "" "1" "00002989" "TDRKH" "transcript variant 3" "002" "NM_006862.3" "" "NP_006853.2" "" "" "" "-182" "2148" "1686" "151763010" "151744040" "00001" "2013-11-15 16:28:31" "" "" "" "1" "00002990" "TDRKH" "transcript variant 2" "003" "NM_001083963.1" "" "NP_001077432.1" "" "" "" "-157" "2659" "1686" "151763010" "151745955" "00001" "2013-11-15 16:28:31" "" "" "" "1" "00002991" "TDRKH" "transcript variant 4" "004" "NM_001083964.1" "" "NP_001077433.1" "" "" "" "-182" "2524" "1551" "151763010" "151745955" "00001" "2013-11-15 16:28:31" "" "" "" "1" "00002992" "TDRKH" "transcript variant 1" "005" "NM_001083965.1" "" "NP_001077434.1" "" "" "" "-182" "2659" "1686" "151763010" "151745955" "00001" "2013-11-15 16:28:31" "" "" "" "1" "00002993" "TDRKH" "transcript variant X2" "006" "XM_005244854.1" "" "XP_005244911.1" "" "" "" "-224" "2469" "1686" "151763052" "151745960" "00001" "2013-11-15 16:28:31" "" "" "" "1" "00002994" "TDRKH" "transcript variant X3" "007" "XM_005244855.1" "" "XP_005244912.1" "" "" "" "-138" "2642" "1674" "151762985" "151745960" "00001" "2013-11-15 16:28:31" "" "" "" "1" "00002995" "TDRKH" "transcript variant X4" "008" "XM_005244856.1" "" "XP_005244913.1" "" "" "" "-702" "1797" "1014" "151762983" "151745960" "00001" "2013-11-15 16:28:31" "" "" "" "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