### LOVD-version 3000-210 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = CCDC90B) # 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}}" "CCDC90B" "coiled-coil domain containing 90B" "11" "q14.1" "unknown" "NC_000011.9" "UD_138455007965" "" "" "" "1" "1" "28108" "60492" "" "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 = 11 "{{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}}" "00001693" "CCDC90B" "transcript variant X1" "001" "XM_005274151.1" "" "" "" "" "" "1" "1415" "1415" "82997437" "82972498" "00001" "2013-11-15 15:14:55" "" "" "" "11" "00001694" "CCDC90B" "transcript variant X10" "002" "XM_005274160.1" "" "XP_005274217.1" "" "" "" "-499" "875" "420" "82997393" "82972498" "00001" "2013-11-15 15:14:55" "" "" "" "11" "00001695" "CCDC90B" "transcript variant X4" "003" "XM_005274154.1" "" "XP_005274211.1" "" "" "" "-884" "926" "471" "82997389" "82972498" "00001" "2013-11-15 15:14:55" "" "" "" "11" "00001696" "CCDC90B" "transcript variant X7" "004" "XM_005274157.1" "" "XP_005274214.1" "" "" "" "-997" "917" "462" "82997389" "82972498" "00001" "2013-11-15 15:14:55" "" "" "" "11" "00001697" "CCDC90B" "transcript variant X3" "005" "XM_005274153.1" "" "XP_005274210.1" "" "" "" "-311" "926" "471" "82997136" "82972498" "00001" "2013-11-15 15:14:55" "" "" "" "11" "00001698" "CCDC90B" "transcript variant X6" "006" "XM_005274156.1" "" "XP_005274213.1" "" "" "" "-716" "926" "471" "82997136" "82972498" "00001" "2013-11-15 15:14:55" "" "" "" "11" "00001699" "CCDC90B" "transcript variant X8" "007" "XM_005274158.1" "" "XP_005274215.1" "" "" "" "-1170" "917" "462" "82997136" "82972498" "00001" "2013-11-15 15:14:55" "" "" "" "11" "00001700" "CCDC90B" "transcript variant X9" "008" "XM_005274159.1" "" "XP_005274216.1" "" "" "" "-404" "917" "462" "82997031" "82972498" "00001" "2013-11-15 15:14:55" "" "" "" "11" "00001701" "CCDC90B" "transcript variant X5" "009" "XM_005274155.1" "" "XP_005274212.1" "" "" "" "-905" "926" "471" "82996984" "82972498" "00001" "2013-11-15 15:14:55" "" "" "" "11" "00001702" "CCDC90B" "transcript variant X2" "010" "XM_005274152.1" "" "XP_005274209.1" "" "" "" "-430" "1101" "621" "82997445" "82972502" "00001" "2013-11-15 15:14:55" "" "" "" "11" "00001703" "CCDC90B" "coiled-coil domain containing 90B" "011" "NM_021825.3" "" "NP_068597.2" "" "" "" "-362" "1212" "765" "82997377" "82972506" "00001" "2013-11-15 15:14:55" "" "" "" "11" ## 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