### LOVD-version 3000-210 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = PHYHIPL) # 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}}" "PHYHIPL" "phytanoyl-CoA 2-hydroxylase interacting protein-like" "10" "q21.1" "unknown" "NC_000010.10" "UD_138455370292" "" "" "" "1" "1" "29378" "84457" "" "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 = 5 "{{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}}" "00002630" "PHYHIPL" "transcript variant 1" "001" "NM_032439.3" "" "NP_115815.2" "" "" "" "-266" "3314" "1131" "60936348" "61007534" "00001" "2013-11-15 16:15:11" "" "" "" "10" "00002631" "PHYHIPL" "transcript variant 2" "002" "NM_001143774.1" "" "NP_001137246.1" "" "" "" "-124" "3236" "1053" "60937227" "61007534" "00001" "2013-11-15 16:15:11" "" "" "" "10" "00002632" "PHYHIPL" "transcript variant X1" "003" "XM_005270226.1" "" "XP_005270283.1" "" "" "" "-9" "3502" "1038" "60943413" "61007815" "00001" "2013-11-15 16:15:11" "" "" "" "10" "00002633" "PHYHIPL" "transcript variant X3" "004" "XM_005270228.1" "" "XP_005270285.1" "" "" "" "-118" "3457" "993" "60966519" "61007815" "00001" "2013-11-15 16:15:11" "" "" "" "10" "00002634" "PHYHIPL" "transcript variant X2" "005" "XM_005270227.1" "" "XP_005270284.1" "" "" "" "-41" "3457" "993" "60978987" "61007815" "00001" "2013-11-15 16:15:11" "" "" "" "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