### LOVD-version 3000-210 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = HK1) # 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}}" "HK1" "hexokinase 1" "10" "q22" "unknown" "NC_000010.10" "UD_138305756170" "" "" "" "1" "1" "4922" "3098" "142600" "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 21:25:34" "" "" "" "" "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}}" "00000807" "HK1" "transcript variant X2" "001" "XM_005269736.1" "" "XP_005269793.1" "" "" "" "-198" "3513" "2766" "71029740" "71161638" "00001" "2013-11-12 21:41:34" "" "" "" "10" "00000808" "HK1" "transcript variant 5" "002" "NM_033500.2" "" "NP_277035.2" "" "" "" "-499" "3465" "2718" "71029756" "71161638" "00001" "2013-11-12 21:41:34" "" "" "" "10" "00000809" "HK1" "transcript variant 4" "003" "NM_033498.2" "" "NP_277033.1" "" "" "" "-358" "3513" "2766" "71029756" "71161638" "00001" "2013-11-12 21:41:34" "" "" "" "10" "00000810" "HK1" "transcript variant 3" "004" "NM_033497.2" "" "NP_277032.1" "" "" "" "-304" "3513" "2766" "71029756" "71161638" "00001" "2013-11-12 21:41:34" "" "" "" "10" "00000811" "HK1" "transcript variant 2" "005" "NM_033496.2" "" "NP_277031.1" "" "" "" "-101" "3498" "2751" "71075610" "71161638" "00001" "2013-11-12 21:41:34" "" "" "" "10" "00000812" "HK1" "transcript variant X1" "006" "XM_005269735.1" "" "XP_005269792.1" "" "" "" "1" "3630" "2883" "71077800" "71161638" "00001" "2013-11-12 21:41:34" "" "" "" "10" "00000813" "HK1" "transcript variant 1" "007" "NM_000188.2" "" "NP_000179.2" "" "" "" "-101" "3501" "2754" "71078603" "71161638" "00001" "2013-11-12 21:41:34" "" "" "" "10" "00000814" "HK1" "transcript variant X3" "008" "XM_005269737.1" "" "XP_005269794.1" "" "" "" "-456" "3417" "2670" "71097998" "71161638" "00001" "2013-11-12 21:41:34" "" "" "" "10" ## 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