### LOVD-version 3000-30b ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = GRPR) # 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}}" "GRPR" "gastrin-releasing peptide receptor" "X" "p22.2" "unknown" "NG_012512.1" "UD_132118960496" "" "https://www.LOVD.nl/GRPR" "" "1" "4609" "2925" "305670" "1" "1" "1" "1" "This gene sequence variant database has been initiated based on the data reported by Tarpey et al. (2009) A systematic, large-scale resequencing screen of the X-chromosome coding exons in mental retardation. Nat.Genet. 41: 535-543. Establishment of the database was supported by the European Community\'s Seventh Framework Programme (FP7/2007-2013) under grant agreement No 200754 - the GEN2PHEN project." "" "g" "https://databases.lovd.nl/shared/refseq/GRPR_codingDNA.html" "1" "" "" "-1" "" "-1" "00000" "2009-03-06 00:00:00" "00006" "2022-01-23 16:30:00" "00000" "2024-04-19 20:27:30" ## 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}}" "00000667" "GRPR" "gastrin-releasing peptide receptor" "001" "NM_005314.2" "" "NP_005305.1" "" "" "" "-653" "2028" "1155" "16141424" "16171641" "00000" "2012-09-13 12:45:29" "" "" ## Diseases ## Do not remove or alter this header ## ## Count = 3 "{{id}}" "{{symbol}}" "{{name}}" "{{inheritance}}" "{{id_omim}}" "{{tissues}}" "{{features}}" "{{remarks}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "00187" "MRX;IDX" "mental retardation, X-linked (MRX, intellectual disability (IDX))" "" "" "" "X-linked" "" "00006" "2013-09-05 15:56:47" "00006" "2018-12-18 09:23:21" "01157" "CHTE" "Hypothyroidism, central, testicular enlargement (CHTE)" "XLR" "300888" "" "" "" "00006" "2014-09-25 23:29:40" "00006" "2021-12-10 21:51:32" "05324" "DMD" "dystrophy, muscular, Duchenne type (DMD)" "XLR" "310200" "" "" "" "00006" "2017-09-01 17:41:21" "00006" "2021-12-10 21:51:32" ## Genes_To_Diseases ## Do not remove or alter this header ## ## Count = 0 ## Individuals ## Do not remove or alter this header ## ## Count = 8 "{{id}}" "{{fatherid}}" "{{motherid}}" "{{panelid}}" "{{panel_size}}" "{{license}}" "{{owned_by}}" "{{Individual/Reference}}" "{{Individual/Remarks}}" "{{Individual/Gender}}" "{{Individual/Consanguinity}}" "{{Individual/Origin/Geographic}}" "{{Individual/Age_of_death}}" "{{Individual/VIP}}" "{{Individual/Data_av}}" "{{Individual/Treatment}}" "{{Individual/Origin/Population}}" "{{Individual/Individual_ID}}" "00000208" "" "" "" "1" "" "00037" "{PMID:Sun 2011:23143598}, {DOI:Sun 2011:10.1038/ng.2453}" "" "M" "no" "Netherlands" "" "0" "" "" "" "" "00000209" "" "" "" "1" "" "00037" "{PMID:Sun 2011:23143598}, {DOI:Sun 2011:10.1038/ng.2453}" "" "M" "no" "Netherlands" "" "0" "" "" "" "" "00172592" "" "" "" "3" "" "00124" "{PMID:Tarpey 2009:19377476}" "" "M" "" "" "" "0" "for details contact Lucy Raymond (flr24 @ cam.ac.uk)" "" "" "19377476-Pat?" "00172593" "" "" "" "37" "" "00124" "{PMID:Tarpey 2009:19377476}" "" "M" "" "" "" "0" "for details contact Lucy Raymond (flr24 @ cam.ac.uk)" "" "" "19377476-Pat?" "00172594" "" "" "" "49" "" "00124" "{PMID:Tarpey 2009:19377476}" "" "M" "" "" "" "0" "for details contact Lucy Raymond (flr24 @ cam.ac.uk)" "" "" "19377476-Pat?" "00172595" "" "" "" "1" "" "00124" "{PMID:Tarpey 2009:19377476}" "" "M" "" "" "" "0" "for details contact Lucy Raymond (flr24 @ cam.ac.uk)" "" "" "19377476-Pat?" "00172596" "" "" "" "1" "" "00124" "{PMID:Tarpey 2009:19377476}" "" "M" "" "" "" "0" "for details contact Lucy Raymond (flr24 @ cam.ac.uk)" "" "" "19377476-Pat?" "00399872" "" "" "" "1" "" "00006" "{PMID:Falzarano 2021:35047845}" "2-generation family, 1 affected, unaffected carrier mother" "M" "" "" "" "0" "" "" "" "FamPatSE" ## Individuals_To_Diseases ## Do not remove or alter this header ## ## Count = 8 "{{individualid}}" "{{diseaseid}}" "00000208" "01157" "00000209" "01157" "00172592" "00187" "00172593" "00187" "00172594" "00187" "00172595" "00187" "00172596" "00187" "00399872" "05324" ## Phenotypes ## Do not remove or alter this header ## ## Note: Only showing Phenotype columns active for Diseases 00187, 01157, 05324 ## Count = 8 "{{id}}" "{{diseaseid}}" "{{individualid}}" "{{owned_by}}" "{{Phenotype/Inheritance}}" "{{Phenotype/Age}}" "{{Phenotype/Additional}}" "{{Phenotype/Age/Onset}}" "{{Phenotype/Birth/Gestational_age_wk}}" "{{Phenotype/Age/Diagnosis}}" "{{Phenotype/Onset}}" "{{Phenotype/Protein}}" "{{Phenotype/Enzyme/CPK}}" "{{Phenotype/Heart/Myocardium}}" "{{Phenotype/Lung}}" "{{Phenotype/Diagnosis/Definite}}" "{{Phenotype/Diagnosis/Initial}}" "0000038983" "01157" "00000208" "00006" "Familial, X-linked recessive" "" "central hypothyroidism (FT4 0.50-0.99of lower limit normal), no prolactin deficiency, age sonographic determination testicular volume 17.64y, testicular volume right/left 21/20 (7.3–16ml)" "" "" "3w" "" "" "" "" "" "" "" "0000038984" "01157" "00000209" "00006" "Familial, X-linked recessive" "" "central hypothyroidism (FT4 0.50-0.99of lower limit normal), prolactin deficiency, age sonographic determination testicular volume 21.36y, testicular volume right/left 30/26 (8.5–18.3ml)" "" "" "07y04m" "" "" "" "" "" "" "" "0000137456" "00187" "00172592" "00124" "Familial, X-linked" "" "" "" "" "" "" "" "" "" "" "" "MRX" "0000137457" "00187" "00172593" "00124" "Familial, X-linked" "" "" "" "" "" "" "" "" "" "" "" "MRX" "0000137458" "00187" "00172594" "00124" "Familial, X-linked" "" "" "" "" "" "" "" "" "" "" "" "MRX" "0000137459" "00187" "00172595" "00124" "Familial, X-linked" "" "" "" "" "" "" "" "" "" "" "" "MRX" "0000137460" "00187" "00172596" "00124" "Familial, X-linked" "" "" "" "" "" "" "" "" "" "" "" "MRX" "0000292912" "05324" "00399872" "00006" "Familial, X-linked recessive" "" "see paper; ..." "" "" "" "" "" "" "" "" "DMD" "Duchenne muscular dystrophy" ## Screenings ## Do not remove or alter this header ## ## Count = 8 "{{id}}" "{{individualid}}" "{{variants_found}}" "{{owned_by}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "{{Screening/Technique}}" "{{Screening/Template}}" "{{Screening/Tissue}}" "{{Screening/Remarks}}" "0000000209" "00000208" "1" "00037" "00001" "2012-09-13 12:02:03" "" "" "SEQ-NG-I" "DNA" "" "" "0000000210" "00000209" "1" "00037" "00001" "2012-09-13 12:09:36" "" "" "SEQ-NG-I" "DNA" "" "" "0000173475" "00172592" "1" "00124" "00006" "2009-04-08 14:01:02" "00006" "2009-05-19 12:34:20" "SEQ" "DNA" "" "" "0000173476" "00172593" "1" "00124" "00006" "2009-04-08 14:01:02" "00006" "2009-05-19 12:34:20" "SEQ" "DNA" "" "" "0000173477" "00172594" "1" "00124" "00006" "2009-04-08 14:01:02" "00006" "2009-05-19 12:34:20" "SEQ" "DNA" "" "" "0000173478" "00172595" "1" "00124" "00006" "2009-04-08 14:01:02" "00006" "2009-05-19 12:33:15" "SEQ" "DNA" "" "" "0000173479" "00172596" "1" "00124" "00006" "2009-04-08 14:01:02" "00006" "2009-05-19 12:33:15" "SEQ" "DNA" "" "" "0000401115" "00399872" "1" "00006" "00006" "2022-01-23 16:38:36" "" "" "PCR;RT-PCR;SEQ" "DNA;RNA" "" "WGS" ## Screenings_To_Genes ## Do not remove or alter this header ## ## Count = 7 "{{screeningid}}" "{{geneid}}" "0000173475" "GRPR" "0000173476" "GRPR" "0000173477" "HCFC1" "0000173478" "HCFC1" "0000173479" "HCFC1" "0000401115" "DMD" "0000401115" "GRPR" ## 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 = 25 "{{id}}" "{{allele}}" "{{effectid}}" "{{chromosome}}" "{{position_g_start}}" "{{position_g_end}}" "{{type}}" "{{average_frequency}}" "{{owned_by}}" "{{VariantOnGenome/DBID}}" "{{VariantOnGenome/DNA}}" "{{VariantOnGenome/Frequency}}" "{{VariantOnGenome/Reference}}" "{{VariantOnGenome/Restriction_site}}" "{{VariantOnGenome/Published_as}}" "{{VariantOnGenome/Remarks}}" "{{VariantOnGenome/Genetic_origin}}" "{{VariantOnGenome/Segregation}}" "{{VariantOnGenome/dbSNP}}" "{{VariantOnGenome/VIP}}" "{{VariantOnGenome/Methylation}}" "{{VariantOnGenome/ISCN}}" "{{VariantOnGenome/DNA/hg38}}" "{{VariantOnGenome/ClinVar}}" "{{VariantOnGenome/ClinicalClassification}}" "{{VariantOnGenome/ClinicalClassification/Method}}" "0000001810" "20" "50" "X" "16171604" "16171604" "del" "0" "00037" "GRPR_000001" "g.16171604del" "" "" "" "" "" "Germline" "" "" "" "" "" "g.16153481del" "" "VUS" "" "0000002811" "20" "50" "X" "16171594" "16171594" "del" "0" "00037" "GRPR_000003" "g.16171594del" "" "" "" "" "" "Germline" "" "" "" "" "" "g.16153471del" "" "VUS" "" "0000008470" "20" "50" "X" "16171604" "16171604" "del" "0" "00037" "GRPR_000001" "g.16171604del" "" "" "" "" "" "Germline" "" "" "" "" "" "g.16153481del" "" "VUS" "" "0000010815" "20" "50" "X" "16171594" "16171594" "del" "0" "00037" "GRPR_000003" "g.16171594del" "" "" "" "" "" "Germline" "" "" "" "" "" "g.16153471del" "" "VUS" "" "0000281191" "0" "10" "X" "16168467" "16168467" "subst" "0.298295" "02325" "GRPR_000005" "g.16168467T>C" "" "" "" "GRPR(NM_005314.3):c.453T>C (p.S151=)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.16150344T>C" "" "benign" "" "0000281192" "0" "10" "X" "16168677" "16168677" "subst" "0.330017" "02325" "GRPR_000007" "g.16168677T>C" "" "" "" "GRPR(NM_005314.3):c.663T>C (p.I221=)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.16150554T>C" "" "benign" "" "0000288872" "0" "50" "X" "16142092" "16142092" "subst" "0" "01943" "GRPR_000004" "g.16142092T>C" "" "" "" "GRPR(NM_005314.2):c.16T>C (p.C6R)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.16123969T>C" "" "VUS" "" "0000333264" "0" "50" "X" "16168555" "16168555" "subst" "0.000302524" "01804" "GRPR_000006" "g.16168555C>T" "" "" "" "GRPR(NM_005314.2):c.541C>T (p.(Leu181Phe))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.16150432C>T" "" "VUS" "" "0000349182" "0" "10" "X" "16142318" "16142318" "subst" "0.000134657" "02327" "GRPR_000008" "g.16142318G>A" "" "" "" "GRPR(NM_005314.2):c.242G>A (p.S81N)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.16124195G>A" "" "benign" "" "0000393332" "1" "30" "X" "16142472" "16142472" "subst" "0.00833873" "00124" "GRPR_000009" "g.16142472G>A" "3/208 cases" "{PMID:Tarpey 2009:19377476}" "" "T132T" "recurrent, found 3 times" "Germline" "" "" "0" "" "" "g.16124349G>A" "" "likely benign" "" "0000393333" "1" "30" "X" "16168467" "16168467" "subst" "0.298295" "00124" "GRPR_000005" "g.16168467T>C" "37/208 cases" "{PMID:Tarpey 2009:19377476}" "" "S151S" "recurrent, found 37 times" "Germline" "" "" "0" "" "" "g.16150344T>C" "" "likely benign" "" "0000393334" "1" "30" "X" "16168677" "16168677" "subst" "0.330017" "00124" "GRPR_000007" "g.16168677T>C" "49/208 cases" "{PMID:Tarpey 2009:19377476}" "" "I221I" "recurrent, found 49 times" "Germline" "" "" "0" "" "" "g.16150554T>C" "" "likely benign" "" "0000393335" "1" "50" "X" "16168705" "16168705" "subst" "0" "00124" "GRPR_000010" "g.16168705T>C" "1/208 cases" "{PMID:Tarpey 2009:19377476}" "" "" "found once, nonrecurrent change" "Germline" "" "" "0" "" "" "g.16150582T>C" "" "VUS" "" "0000393336" "1" "30" "X" "16168734" "16168734" "subst" "0.000181096" "00124" "GRPR_000011" "g.16168734T>C" "1/208 cases" "{PMID:Tarpey 2009:19377476}" "" "S240S" "found once, nonrecurrent change" "Germline" "" "" "0" "" "" "g.16150611T>C" "" "likely benign" "" "0000575077" "0" "30" "X" "16142093" "16142093" "subst" "0.000848868" "01804" "GRPR_000012" "g.16142093G>C" "" "" "" "GRPR(NM_005314.3):c.17G>C (p.(Cys6Ser))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.16123970G>C" "" "likely benign" "" "0000575080" "0" "50" "X" "16170613" "16170613" "subst" "1.68119E-5" "01943" "GRPR_000015" "g.16170613A>G" "" "" "" "GRPR(NM_005314.2):c.1000A>G (p.N334D)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "g.16152490A>G" "" "VUS" "" "0000682305" "0" "50" "X" "16142431" "16142431" "subst" "3.92672E-5" "01943" "GRPR_000016" "g.16142431A>G" "" "" "" "GRPR(NM_005314.2):c.355A>G (p.I119V)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000693497" "0" "30" "X" "16170516" "16170516" "subst" "2.79968E-5" "01943" "GRPR_000017" "g.16170516T>C" "" "" "" "GRPR(NM_005314.2):c.903T>C (p.F301=)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0000728712" "0" "30" "X" "16142318" "16142318" "subst" "0.000134657" "01943" "GRPR_000008" "g.16142318G>A" "" "" "" "GRPR(NM_005314.2):c.242G>A (p.S81N)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0000810192" "0" "50" "X" "16170535" "16170535" "subst" "0" "01943" "GRPR_000018" "g.16170535C>T" "" "" "" "GRPR(NM_005314.2):c.922C>T (p.R308C)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0000834202" "21" "90" "X" "16147079" "31662544" "inv" "0" "00006" "DMD_068401" "g.16147079_31662544inv" "" "{PMID:Falzarano 2021:35047845}" "" "g.16147177_31662545inv" "" "Germline" "" "" "0" "" "" "g.16128956_31644427inv" "" "pathogenic (recessive)" "" "0000856484" "0" "30" "X" "16170699" "16170699" "subst" "8.42971E-5" "01943" "GRPR_000022" "g.16170699G>A" "" "" "" "GRPR(NM_005314.2):c.1086G>A (p.K362=)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0000867238" "0" "30" "X" "16142147" "16142147" "subst" "2.80355E-5" "01943" "GRPR_000019" "g.16142147A>C" "" "" "" "GRPR(NM_005314.2):c.71A>C (p.H24P)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0000867239" "0" "30" "X" "16168497" "16168497" "subst" "3.37037E-5" "01943" "GRPR_000020" "g.16168497C>T" "" "" "" "GRPR(NM_005314.2):c.483C>T (p.A161=)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" "0000867240" "0" "50" "X" "16170653" "16170653" "subst" "2.24325E-5" "01943" "GRPR_000021" "g.16170653G>A" "" "" "" "GRPR(NM_005314.2):c.1040G>A (p.R347Q)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" ## 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 GRPR ## Count = 25 "{{id}}" "{{transcriptid}}" "{{effectid}}" "{{position_c_start}}" "{{position_c_start_intron}}" "{{position_c_end}}" "{{position_c_end_intron}}" "{{VariantOnTranscript/DNA}}" "{{VariantOnTranscript/RNA}}" "{{VariantOnTranscript/Protein}}" "{{VariantOnTranscript/Exon}}" "0000001810" "00000667" "50" "1991" "0" "1991" "0" "c.*836del" "r.(=)" "p.(=)" "" "0000002811" "00000667" "50" "1981" "0" "1981" "0" "c.*826del" "r.(=)" "p.(=)" "" "0000008470" "00000667" "50" "1991" "0" "1991" "0" "c.*836del" "r.(=)" "p.(=)" "" "0000010815" "00000667" "50" "1981" "0" "1981" "0" "c.*826del" "r.(=)" "p.(=)" "" "0000281191" "00000667" "10" "453" "0" "453" "0" "c.453T>C" "r.(?)" "p.(Ser151=)" "" "0000281192" "00000667" "10" "663" "0" "663" "0" "c.663T>C" "r.(?)" "p.(Ile221=)" "" "0000288872" "00000667" "50" "16" "0" "16" "0" "c.16T>C" "r.(?)" "p.(Cys6Arg)" "" "0000333264" "00000667" "50" "541" "0" "541" "0" "c.541C>T" "r.(?)" "p.(Leu181Phe)" "" "0000349182" "00000667" "10" "242" "0" "242" "0" "c.242G>A" "r.(?)" "p.(Ser81Asn)" "" "0000393332" "00000667" "30" "396" "0" "396" "0" "c.396G>A" "r.(=)" "p.(=)" "" "0000393333" "00000667" "30" "453" "0" "453" "0" "c.453T>C" "r.(=)" "p.(=)" "" "0000393334" "00000667" "30" "663" "0" "663" "0" "c.663T>C" "r.(=)" "p.(=)" "" "0000393335" "00000667" "50" "691" "0" "691" "0" "c.691T>C" "r.(?)" "p.(Tyr231His)" "" "0000393336" "00000667" "30" "720" "0" "720" "0" "c.720T>C" "r.(=)" "p.(=)" "" "0000575077" "00000667" "30" "17" "0" "17" "0" "c.17G>C" "r.(?)" "p.(Cys6Ser)" "" "0000575080" "00000667" "50" "1000" "0" "1000" "0" "c.1000A>G" "r.(?)" "p.(Asn334Asp)" "" "0000682305" "00000667" "50" "355" "0" "355" "0" "c.355A>G" "r.(?)" "p.(Ile119Val)" "" "0000693497" "00000667" "30" "903" "0" "903" "0" "c.903T>C" "r.(?)" "p.(Phe301=)" "" "0000728712" "00000667" "30" "242" "0" "242" "0" "c.242G>A" "r.(?)" "p.(Ser81Asn)" "" "0000810192" "00000667" "50" "922" "0" "922" "0" "c.922C>T" "r.(?)" "p.(Arg308Cys)" "" "0000834202" "00000667" "90" "0" "0" "0" "0" "c.413+4590_873{1}inv" "r.-653_413::[NM_004006.2:r.8028_*2691]" "p.?" "1i_3_" "0000856484" "00000667" "30" "1086" "0" "1086" "0" "c.1086G>A" "r.(?)" "p.(Lys362=)" "" "0000867238" "00000667" "30" "71" "0" "71" "0" "c.71A>C" "r.(?)" "p.(His24Pro)" "" "0000867239" "00000667" "30" "483" "0" "483" "0" "c.483C>T" "r.(?)" "p.(Ala161=)" "" "0000867240" "00000667" "50" "1040" "0" "1040" "0" "c.1040G>A" "r.(?)" "p.(Arg347Gln)" "" ## Screenings_To_Variants ## Do not remove or alter this header ## ## Count = 10 "{{screeningid}}" "{{variantid}}" "0000000209" "0000001810" "0000000209" "0000002811" "0000000210" "0000008470" "0000000210" "0000010815" "0000173475" "0000393332" "0000173476" "0000393333" "0000173477" "0000393334" "0000173478" "0000393335" "0000173479" "0000393336" "0000401115" "0000834202"