### LOVD-version 3000-210 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = TMEM91) # 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}}" "TMEM91" "transmembrane protein 91" "19" "q13.2" "unknown" "NC_000019.9" "UD_138431511184" "" "" "" "1" "1" "32393" "641649" "" "1" "1" "1" "MSeqDR-LSDB" "Variations Associated with Mitochondrial Diseases Gene" "" "" "2" " ; MitoPhenome http://mitophenome.org " "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 = 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}}" "00001221" "TMEM91" "transcript variant X1" "001" "XM_005259150.1" "" "XP_005259207.1" "" "" "" "-264" "729" "519" "41856873" "41889988" "00001" "2013-11-12 21:58:45" "" "" "" "19" "00001222" "TMEM91" "transcript variant 6" "002" "NM_001098825.1" "" "NP_001092295.1" "" "" "" "-159" "581" "402" "41869871" "41889988" "00001" "2013-11-12 21:58:45" "" "" "" "19" "00001223" "TMEM91" "transcript variant 1" "003" "NM_001098821.1" "" "NP_001092291.1" "" "" "" "-351" "729" "519" "41882438" "41889988" "00001" "2013-11-12 21:58:45" "" "" "" "19" "00001224" "TMEM91" "transcript variant 3" "004" "NM_001098822.1" "" "NP_001092292.1" "" "" "" "-351" "581" "402" "41882438" "41889988" "00001" "2013-11-12 21:58:45" "" "" "" "19" "00001225" "TMEM91" "transcript variant 4" "005" "NM_001098823.1" "" "NP_001092293.1" "" "" "" "-351" "570" "384" "41882438" "41889988" "00001" "2013-11-12 21:58:45" "" "" "" "19" "00001226" "TMEM91" "transcript variant 5" "006" "NM_001098824.1" "" "NP_001092294.1" "" "" "" "-351" "558" "372" "41882438" "41889988" "00001" "2013-11-12 21:58:45" "" "" "" "19" "00001227" "TMEM91" "transcript variant X2" "007" "XM_005259151.1" "" "XP_005259208.1" "" "" "" "-485" "729" "519" "41882773" "41889988" "00001" "2013-11-12 21:58:45" "" "" "" "19" "00001228" "TMEM91" "transcript variant 2" "008" "NM_001042595.2" "" "NP_001036060.1" "" "" "" "-89" "883" "420" "41883169" "41889988" "00001" "2013-11-12 21:58:45" "" "" "" "19" ## 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