### LOVD-version 3000-210 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = CCT7) # 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}}" "CCT7" "chaperonin containing TCP1, subunit 7 (eta)" "2" "p13.2" "unknown" "NC_000002.11" "UD_132464786767" "" "" "" "1" "1" "1622" "10574" "605140" "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 15:07:22" "" "" "" "" "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 = 6 "{{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}}" "00001704" "CCT7" "transcript variant 4" "001" "NM_001166285.1" "" "NP_001159757.1" "" "" "" "-371" "1661" "1500" "73461364" "73480150" "00001" "2013-11-15 15:15:00" "" "" "" "2" "00001705" "CCT7" "transcript variant 1" "002" "NM_006429.3" "" "NP_006420.1" "" "" "" "-143" "1793" "1632" "73461364" "73480150" "00001" "2013-11-15 15:15:00" "" "" "" "2" "00001706" "CCT7" "transcript variant 5" "003" "NR_029402.1" "" "" "" "" "" "1" "1883" "1883" "73461364" "73480150" "00001" "2013-11-15 15:15:00" "" "" "" "2" "00001707" "CCT7" "transcript variant 6" "004" "NR_029403.1" "" "" "" "" "" "1" "1787" "1787" "73461364" "73480150" "00001" "2013-11-15 15:15:00" "" "" "" "2" "00001708" "CCT7" "transcript variant 3" "005" "NM_001166284.1" "" "NP_001159756.1" "" "" "" "-143" "1532" "1371" "73461364" "73480150" "00001" "2013-11-15 15:15:00" "" "" "" "2" "00001709" "CCT7" "transcript variant 2" "006" "NM_001009570.2" "" "NP_001009570.1" "" "" "" "-143" "1181" "1020" "73461364" "73480150" "00001" "2013-11-15 15:15:00" "" "" "" "2" ## 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