### LOVD-version 3000-210 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = PCCB) # 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}}" "PCCB" "propionyl CoA carboxylase, beta polypeptide" "3" "q21-q22" "unknown" "NC_000003.11" "UD_138312274702" "" "" "" "1" "1" "8654" "5096" "232050" "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 = 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}}" "00001036" "PCCB" "transcript variant X4" "001" "XM_005247510.1" "" "XP_005247567.1" "" "" "" "-51" "5434" "1653" "135969167" "136056737" "00001" "2013-11-12 21:53:16" "" "" "" "3" "00001037" "PCCB" "transcript variant X2" "002" "XM_005247508.1" "" "XP_005247565.1" "" "" "" "-51" "1826" "1344" "135969167" "136051431" "00001" "2013-11-12 21:53:16" "" "" "" "3" "00001038" "PCCB" "transcript variant X3" "003" "XM_005247509.1" "" "XP_005247566.1" "" "" "" "-51" "1665" "1218" "135969167" "136049014" "00001" "2013-11-12 21:53:16" "" "" "" "3" "00001039" "PCCB" "transcript variant 2" "004" "NM_001178014.1" "" "NP_001171485.1" "" "" "" "-51" "1825" "1680" "135969167" "136049013" "00001" "2013-11-12 21:53:16" "" "" "" "3" "00001040" "PCCB" "transcript variant 1" "005" "NM_000532.4" "" "NP_000523.2" "" "" "" "-51" "1765" "1620" "135969167" "136049013" "00001" "2013-11-12 21:53:16" "" "" "" "3" "00001041" "PCCB" "transcript variant X1" "006" "XM_005247507.1" "" "XP_005247564.1" "" "" "" "-40" "1490" "1344" "135969178" "136049014" "00001" "2013-11-12 21:53:16" "" "" "" "3" ## 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