### LOVD-version 3000-290 ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = MMP9) # 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}}" "{{id_hgnc}}" "{{id_entrez}}" "{{id_omim}}" "{{show_hgmd}}" "{{show_genecards}}" "{{show_genetests}}" "{{show_orphanet}}" "{{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}}" "MMP9" "matrix metallopeptidase 9" "20" "q13.12" "unknown" "NG_011468.1" "UD_144427087451" "" "" "" "1" "7176" "4318" "120361" "1" "1" "1" "0" "" "" "" "" "1" "" "" "-1" "" "-1" "00001" "2021-01-05 14:55:37" "" "" "00005" "2021-09-01 12:18:29" ## Transcripts ## Do not remove or alter this header ## ## Count = 1 "{{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}}" "00000090" "MMP9" "matrix metallopeptidase 9" "001" "NM_004994.2" "" "NP_004985.2" "" "" "" "-19" "2317" "2124" "46008908" "46016561" "00001" "2021-01-05 14:55:37" "" "" ## Diseases ## Do not remove or alter this header ## ## Count = 2 "{{id}}" "{{symbol}}" "{{name}}" "{{inheritance}}" "{{id_omim}}" "{{tissues}}" "{{features}}" "{{remarks}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "00054" "EH" "Essential Hypertension" "" "" "" "" "" "00001" "2021-01-05 14:55:18" "" "" "00055" "-" "Nephrolithiasis" "" "" "" "" "" "00001" "2021-01-06 10:24:47" "" "" ## Genes_To_Diseases ## Do not remove or alter this header ## ## Count = 2 "{{geneid}}" "{{diseaseid}}" "MMP9" "00054" "MMP9" "00055" ## Individuals ## Do not remove or alter this header ## ## Count = 2 "{{id}}" "{{fatherid}}" "{{motherid}}" "{{panelid}}" "{{panel_size}}" "{{license}}" "{{owned_by}}" "{{Individual/Reference}}" "{{Individual/Remarks}}" "{{Individual/Remarks_Non_Public}}" "{{Individual/Origin/Geographic}}" "{{Individual/Origin/Ethnic}}" "{{Individual/Origin/Population}}" "{{Individual/Gender}}" "00000319" "" "" "" "1" "" "00002" "{DOI:Farizeh Aalam Ghomi Tabatabae et al. (2018):10.4066/biomedicalresearch.29-17-470}" "" "" "Malaysia" "" "" "M" "00000332" "" "" "" "1" "" "00002" "{PMID:Atheer Awad Mehde et al. (2018):28205286}" "" "" "Malaysia" "" "" "" ## Individuals_To_Diseases ## Do not remove or alter this header ## ## Count = 2 "{{individualid}}" "{{diseaseid}}" "00000319" "00054" "00000332" "00055" ## Phenotypes ## Do not remove or alter this header ## ## Note: Only showing Phenotype columns active for Diseases 00054, 00055 ## Count = 0 ## Screenings ## Do not remove or alter this header ## ## Count = 2 "{{id}}" "{{individualid}}" "{{variants_found}}" "{{owned_by}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "{{Screening/Technique}}" "{{Screening/Template}}" "0000000334" "00000319" "1" "00002" "00002" "2021-01-05 15:28:57" "" "" "PCR" "DNA" "0000000347" "00000332" "1" "00002" "00002" "2021-01-06 14:48:29" "" "" "PCR" "DNA" ## Screenings_To_Genes ## Do not remove or alter this header ## ## Count = 2 "{{screeningid}}" "{{geneid}}" "0000000334" "MMP9" "0000000347" "MMP9" ## 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 = 8 "{{id}}" "{{allele}}" "{{effectid}}" "{{chromosome}}" "{{position_g_start}}" "{{position_g_end}}" "{{type}}" "{{average_frequency}}" "{{owned_by}}" "{{VariantOnGenome/DBID}}" "{{VariantOnGenome/DNA}}" "{{VariantOnGenome/Frequency}}" "{{VariantOnGenome/Reference}}" "{{VariantOnGenome/Published_as}}" "{{VariantOnGenome/Remarks}}" "{{VariantOnGenome/dbSNP}}" "0000001521" "0" "90" "20" "46007337" "46007337" "subst" "0" "00002" "MMP9_000001" "g.46007337C>T" "85/133" "{dbSNP:rs3918242}" "C1562T" "" "rs3918242" "0000001522" "3" "90" "20" "46007337" "46007337" "subst" "0" "00002" "MMP9_000001" "g.46007337C>T" "4/133" "{dbSNP:rs3918242}" "C1562T" "" "rs3918242" "0000001523" "0" "90" "20" "46011586" "46011586" "subst" "0" "00002" "MMP9_000002" "g.46011586A>G" "45/133" "{dbSNP:rs17576}, {ClinVar:338550}" "R279Q" "" "rs17576" "0000001524" "3" "90" "20" "46011586" "46011586" "subst" "0" "00002" "MMP9_000002" "g.46011586A>G" "19/133" "{dbSNP:rs17576}, {ClinVar:338550}" "R279Q" "" "rs17576" "0000001552" "0" "10" "20" "46011586" "46011586" "subst" "0" "00002" "MMP9_000002" "g.46011586A>G" "38/120" "{PMID:Atheer Awad Mehde et al. (2018):28205286}, {dbSNP:rs17576}, {ClinVar:338550}" "R279Q" "" "rs17576" "0000001553" "3" "10" "20" "46011586" "46011586" "subst" "0" "00002" "MMP9_000002" "g.46011586A>G" "22/120" "{PMID:Atheer Awad Mehde et al. (2018):28205286}, {dbSNP:rs17576}, {ClinVar:338550}" "R279Q" "" "rs17576" "0000001554" "0" "90" "20" "46007337" "46007337" "subst" "0" "00002" "MMP9_000001" "g.46007337C>T" "31/120" "{PMID:Atheer Awad Mehde et al. (2018):28205286}, {dbSNP:rs3918242}" "C1562T" "" "rs3918242" "0000001555" "3" "90" "20" "46007337" "46007337" "subst" "0" "00002" "MMP9_000001" "g.46007337C>T" "19/120" "{PMID:Atheer Awad Mehde et al. (2018):28205286}, {dbSNP:rs3918242}" "C1562T" "" "rs3918242" ## 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. ## Note: Only showing Variants_On_Transcript columns active for Genes MMP9 ## Count = 8 "{{id}}" "{{transcriptid}}" "{{effectid}}" "{{position_c_start}}" "{{position_c_start_intron}}" "{{position_c_end}}" "{{position_c_end_intron}}" "{{VariantOnTranscript/DNA}}" "{{VariantOnTranscript/Exon}}" "{{VariantOnTranscript/Protein}}" "{{VariantOnTranscript/RNA}}" "{{VariantOnTranscript/Published_as}}" "{{VariantOnTranscript/GVS/Function}}" "{{VariantOnTranscript/VariantOnTranscript}}" "0000001521" "00000090" "90" "-1590" "0" "-1590" "0" "c.-1590C>T" "" "p.(=)" "r.(=)" "" "" "" "0000001522" "00000090" "90" "-1590" "0" "-1590" "0" "c.-1590C>T" "" "p.(=)" "r.(=)" "" "" "" "0000001523" "00000090" "90" "836" "0" "836" "0" "c.836A>G" "" "p.(Gln279Arg)" "r.(?)" "" "" "{ClinVar:338550}" "0000001524" "00000090" "90" "836" "0" "836" "0" "c.836A>G" "" "p.(Gln279Arg)" "r.(?)" "" "" "{ClinVar:338550}" "0000001552" "00000090" "10" "836" "0" "836" "0" "c.836A>G" "" "p.(Gln279Arg)" "r.(?)" "" "" "{ClinVar:338550}" "0000001553" "00000090" "10" "836" "0" "836" "0" "c.836A>G" "" "p.(Gln279Arg)" "r.(?)" "" "" "{ClinVar:338550}" "0000001554" "00000090" "90" "-1590" "0" "-1590" "0" "c.-1590C>T" "" "p.(=)" "r.(=)" "" "" "" "0000001555" "00000090" "90" "-1590" "0" "-1590" "0" "c.-1590C>T" "" "p.(=)" "r.(=)" "" "" "" ## Screenings_To_Variants ## Do not remove or alter this header ## ## Count = 8 "{{screeningid}}" "{{variantid}}" "0000000334" "0000001521" "0000000334" "0000001522" "0000000334" "0000001523" "0000000334" "0000001524" "0000000347" "0000001552" "0000000347" "0000001553" "0000000347" "0000001554" "0000000347" "0000001555"