### LOVD-version 3000-210 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = NEU4) # 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}}" "NEU4" "sialidase 4" "2" "q37.3" "unknown" "NC_000002.11" "UD_138455330652" "" "" "" "1" "1" "21328" "129807" "608527" "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 = 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}}" "00002458" "NEU4" "transcript variant X1" "001" "XM_005246989.1" "" "XP_005247046.1" "" "" "" "-383" "1853" "1485" "242749920" "242758742" "00001" "2013-11-15 16:08:37" "" "" "" "2" "00002459" "NEU4" "transcript variant 4" "002" "NM_001167601.1" "" "NP_001161073.1" "" "" "" "-216" "1820" "1455" "242750160" "242758739" "00001" "2013-11-15 16:08:37" "" "" "" "2" "00002460" "NEU4" "transcript variant 3" "003" "NM_001167600.1" "" "NP_001161072.1" "" "" "" "-213" "1820" "1455" "242750160" "242758739" "00001" "2013-11-15 16:08:37" "" "" "" "2" "00002461" "NEU4" "transcript variant 5" "004" "NM_001167602.1" "" "NP_001161074.1" "" "" "" "-711" "1820" "1455" "242752030" "242758739" "00001" "2013-11-15 16:08:37" "" "" "" "2" "00002462" "NEU4" "transcript variant 2" "005" "NM_001167599.1" "" "NP_001161071.1" "" "" "" "-494" "1859" "1494" "242752030" "242758739" "00001" "2013-11-15 16:08:37" "" "" "" "2" "00002463" "NEU4" "transcript variant 1" "006" "NM_080741.2" "" "NP_542779.2" "" "" "" "-494" "1856" "1491" "242752030" "242758739" "00001" "2013-11-15 16:08:37" "" "" "" "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