### LOVD-version 3000-30b ### Full data download ### To import, do not remove or alter this header ### ## Filter: (gene_public = PTHLH) # 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}}" "PTHLH" "parathyroid hormone-like hormone" "12" "p12.1-p11.2" "unknown" "NG_023197.1" "UD_132119107432" "" "http://www.LOVD.nl/PTHLH" "" "1" "9607" "5744" "168470" "1" "1" "1" "1" "Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland." "" "g" "http://databases.lovd.nl/shared/refseq/PTHLH_codingDNA.html" "1" "" "" "-1" "" "-1" "00001" "2010-04-29 00:00:00" "00006" "2016-05-09 21:10:00" "00000" "2025-05-05 21:14:00" ## 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}}" "00017118" "PTHLH" "transcript variant 1" "001" "NM_198965.1" "" "NP_945316.1" "" "" "" "-322" "1009" "534" "28124916" "28111017" "" "0000-00-00 00:00:00" "" "" ## 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}}" "03320" "BDE2" "brachydactyly type E2 (BD-E2)" "AD" "613382" "" "" "" "00006" "2014-09-25 23:29:40" "00006" "2021-12-10 21:51:32" "04227" "BD" "brachydactyly (BD)" "" "" "" "" "" "00006" "2015-03-14 21:49:37" "" "" ## Genes_To_Diseases ## Do not remove or alter this header ## ## Count = 1 "{{geneid}}" "{{diseaseid}}" "PTHLH" "03320" ## Individuals ## Do not remove or alter this header ## ## Count = 13 "{{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}}" "00064685" "" "" "" "27" "" "00006" "{PMID:Klopocki 2010:20170896}, DECIPHER:BER251557" "5-generation family, 27 affecteds (14F, 13M)" "F;M" "" "" "" "0" "" "" "European" "" "00064686" "" "" "" "1" "" "00006" "{PMID:Klopocki 2010:20170896}, DECIPHER:BER251557" "3-generation family, 1 affected" "F" "" "" "" "0" "" "" "European" "" "00064687" "" "" "" "1" "" "00006" "{PMID:Klopocki 2010:20170896}, DECIPHER:BER251557" "2-generation family, 1 affected" "F" "" "" "" "0" "" "" "European" "" "00064688" "" "" "" "3" "" "00006" "{PMID:Klopocki 2010:20170896}, DECIPHER:BER251557" "3-generation family, 3 affecteds (2F, M)" "F;M" "" "" "" "0" "" "" "European" "" "00064689" "" "" "" "3" "" "00006" "{PMID:Klopocki 2010:20170896}, DECIPHER:BER251557" "3-generation family, 3 affecteds (2F, M)" "F;M" "" "" "" "0" "" "" "European" "" "00079971" "" "" "" "1" "" "01744" "{PMID:Thomas-Teinturier 2016:26640227}" "Sporadic patient" "F" "no" "Spain" "" "0" "" "" "European" "" "00079974" "" "" "" "2" "" "01744" "{PMID:Thomas-Teinturier 2016:26640227}" "2-generation family, 2 affected (proband: daughter; mother)" "F" "no" "(France)" "" "0" "" "" "" "" "00079975" "" "" "" "1" "" "01744" "{PMID:Jamsheer 2016:26763883}" "Sporadic patient" "F" "" "(Poland)" "" "0" "" "" "" "" "00079979" "" "" "" "1" "" "01744" "" "" "F" "no" "(Spain)" "" "0" "" "" "white" "" "00079980" "" "" "" "3" "" "01744" "{PMID:Jamsheer 2016:26763883}" "2-generation family, 3 affecteds (2 sisters, father)" "F;M" "" "(Poland)" "" "0" "" "" "" "" "00081807" "" "" "" "7" "" "01199" "{PMID:Wang 2015:25801215}" "3-generation family, 7 affecteds (5F, 2M)" "F;M" "no" "China" "" "0" "" "" "" "" "00207697" "" "" "" "2" "" "01744" "NOT PUBLISHED" "2-generation family, 2 affecteds (mother and son)" "F" "?" "" "" "0" "" "" "" "" "00207698" "" "" "00207697" "1" "" "01744" "" "" "M" "?" "" "" "0" "" "" "" "" ## Individuals_To_Diseases ## Do not remove or alter this header ## ## Count = 13 "{{individualid}}" "{{diseaseid}}" "00064685" "03320" "00064686" "03320" "00064687" "03320" "00064688" "03320" "00064689" "03320" "00079971" "03320" "00079974" "03320" "00079975" "03320" "00079979" "03320" "00079980" "03320" "00081807" "03320" "00207697" "04227" "00207698" "04227" ## Phenotypes ## Do not remove or alter this header ## ## Note: Only showing Phenotype columns active for Diseases 03320, 04227 ## Count = 13 "{{id}}" "{{diseaseid}}" "{{individualid}}" "{{owned_by}}" "{{Phenotype/Inheritance}}" "{{Phenotype/Age}}" "{{Phenotype/Additional}}" "{{Phenotype/Age/Onset}}" "{{Phenotype/Age/Diagnosis}}" "{{Phenotype/Onset}}" "{{Phenotype/Protein}}" "{{Phenotype/Enzyme/CPK}}" "{{Phenotype/Heart/Myocardium}}" "{{Phenotype/Lung}}" "{{Phenotype/Diagnosis/Definite}}" "{{Phenotype/Diagnosis/Initial}}" "0000050883" "03320" "00064685" "00006" "Familial, autosomal dominant" "" "see paper; …, learning difficulties, phenotype variable but with complete penetrance" "" "" "" "" "" "" "" "" "" "0000050884" "03320" "00064686" "00006" "Familial, autosomal dominant" "" "see paper; …, tooth problems" "" "" "" "" "" "" "" "" "" "0000050885" "03320" "00064687" "00006" "Familial, autosomal dominant" "" "see paper; …" "" "" "" "" "" "" "" "" "" "0000050886" "03320" "00064688" "00006" "Familial, autosomal dominant" "" "see paper; …" "" "" "" "" "" "" "" "" "" "0000050887" "03320" "00064689" "00006" "Familial, autosomal dominant" "" "see paper; …, hypoplastic nails first fingers" "" "" "" "" "" "" "" "" "" "0000059619" "03320" "00079971" "01744" "Isolated (sporadic)" "11y05m" "" "" "12y" "" "" "" "" "" "" "" "0000059632" "03320" "00079975" "01744" "Isolated (sporadic)" "" "" "" "" "" "" "" "" "" "" "" "0000059633" "03320" "00079974" "01744" "Familial, autosomal dominant" "" "maternally inherited, 2 affected sisters" "" "" "" "" "" "" "" "" "" "0000059635" "03320" "00079979" "01744" "Isolated (sporadic)" "" "Mild overweight, advanced bone age (final height below target height), round face, long philtrum, short neck, descended and widely separated nipples, hyperandrogenism" "" "" "" "" "" "" "" "" "" "0000059636" "03320" "00079980" "01744" "Familial, autosomal dominant" "" "" "" "" "" "" "" "" "" "" "" "0000061452" "03320" "00081807" "00006" "Familial, autosomal dominant" "" "see paper; ..., brachydactyly type E, short stature" "" "" "" "" "" "" "" "" "" "0000155488" "04227" "00207697" "01744" "Unknown" "50y" "HP:0000545 (myopia magna); HP:0004322" "" "50y" "" "" "" "" "" "brachydactyly type E" "brachydactyly type E" "0000155489" "04227" "00207698" "01744" "Familial, autosomal dominant" "09y" "HP:0005863" "" "09y" "HP:0005863" "" "" "" "" "brachydactyly type E" "brachydactyly type E" ## Screenings ## Do not remove or alter this header ## ## Count = 13 "{{id}}" "{{individualid}}" "{{variants_found}}" "{{owned_by}}" "{{created_by}}" "{{created_date}}" "{{edited_by}}" "{{edited_date}}" "{{Screening/Technique}}" "{{Screening/Template}}" "{{Screening/Tissue}}" "{{Screening/Remarks}}" "0000064824" "00064685" "1" "00006" "00115" "2010-07-22 11:33:16" "00006" "2016-05-10 09:20:41" "PCRq;SEQ" "DNA" "" "" "0000064825" "00064686" "1" "00006" "00115" "2010-07-22 11:33:16" "00115" "2010-08-11 09:03:13" "SEQ" "DNA" "" "" "0000064826" "00064687" "1" "00006" "00115" "2010-07-22 11:33:16" "00115" "2010-08-11 09:03:13" "SEQ" "DNA" "" "" "0000064827" "00064688" "1" "00006" "00115" "2010-07-22 11:33:16" "00115" "2010-08-11 09:03:13" "SEQ" "DNA" "" "" "0000064828" "00064689" "1" "00006" "00115" "2010-07-22 11:33:16" "00115" "2010-08-11 09:03:13" "SEQ" "DNA" "" "" "0000080050" "00079971" "1" "01744" "01744" "2016-08-29 17:21:58" "01199" "2016-09-02 12:49:52" "SEQ" "DNA" "peripheral blood" "" "0000080052" "00079974" "1" "01744" "01744" "2016-08-30 09:43:44" "" "" "SEQ" "DNA" "blood" "" "0000080053" "00079975" "1" "01744" "01744" "2016-08-30 10:07:46" "" "" "SEQ" "DNA" "peripheral blood" "" "0000080058" "00079979" "1" "01744" "01744" "2016-08-30 11:04:05" "" "" "SEQ" "DNA" "peripheral blood" "" "0000080059" "00079980" "1" "01744" "01744" "2016-08-30 11:17:41" "" "" "SEQ" "DNA" "peripheral blood" "" "0000081937" "00081807" "1" "01199" "01199" "2016-08-24 19:25:11" "" "" "SEQ" "DNA" "" "" "0000208738" "00207697" "1" "01744" "01199" "2018-11-28 16:37:49" "" "" "SEQ" "DNA" "complete blood" "" "0000208739" "00207698" "1" "01744" "01199" "2018-11-28 16:45:07" "" "" "SEQ" "DNA" "complete blood" "" ## Screenings_To_Genes ## Do not remove or alter this header ## ## Count = 13 "{{screeningid}}" "{{geneid}}" "0000064824" "PTHLH" "0000064825" "PTHLH" "0000064826" "PTHLH" "0000064827" "PTHLH" "0000064828" "PTHLH" "0000080050" "PTHLH" "0000080052" "PTHLH" "0000080053" "PTHLH" "0000080058" "PTHLH" "0000080059" "PTHLH" "0000081937" "PTHLH" "0000208738" "PTHLH" "0000208739" "PTHLH" ## 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 = 21 "{{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}}" "0000096460" "1" "90" "12" "28111491" "28122427" "del" "0" "00006" "PTHLH_000001" "g.(?_28111491)_(28122427_?)del" "" "{PMID:Klopocki 2010:20170896}, DECIPHER:BER251557" "" "" "" "Germline" "yes" "" "0" "" "" "" "" "pathogenic" "" "0000096461" "1" "90" "12" "28116674" "28116674" "subst" "0" "00006" "PTHLH_000002" "g.28116674A>G" "" "{PMID:Klopocki 2010:20170896}, DECIPHER:BER251557" "" "L44P" "" "Germline" "" "" "0" "" "" "g.27963741A>G" "" "pathogenic" "" "0000096462" "1" "90" "12" "28116626" "28116626" "subst" "0" "00006" "PTHLH_000003" "g.28116626A>G" "" "{PMID:Klopocki 2010:20170896}, DECIPHER:BER251557" "" "L60P" "" "Germline" "" "" "0" "" "" "g.27963693A>G" "" "pathogenic" "" "0000096463" "1" "90" "12" "28116447" "28116447" "subst" "0" "00006" "PTHLH_000005" "g.28116447T>A" "" "{PMID:Klopocki 2010:20170896}, DECIPHER:BER251557" "" "T>C (K120X)" "" "Germline" "yes" "" "0" "" "" "g.27963514T>A" "" "pathogenic" "" "0000096464" "1" "90" "12" "28111492" "28111492" "subst" "0" "00006" "PTHLH_000004" "g.28111492T>C" "" "{PMID:Klopocki 2010:20170896}, DECIPHER:BER251557" "" "X178WextX54" "" "Germline" "yes" "" "0" "" "" "g.27958559T>C" "" "pathogenic" "" "0000128926" "0" "70" "12" "28122323" "28122326" "del" "0" "01744" "PTHLH_000010" "g.28122323_28122326del" "" "{PMID:Thomas-Teinturier et al. 2016:26640227}" "" "" "de novo in patient" "De novo" "yes" "" "0" "" "" "g.27969390_27969393del" "" "likely pathogenic" "" "0000128928" "21" "70" "12" "28122258" "28122385" "del" "0" "01744" "PTHLH_000007" "g.28122258_28122385del" "" "{PMID:Thomas-Teinturier et al. 2016:26640227}" "" "47_101+73del128" "" "Germline" "yes" "" "0" "" "" "g.27969325_27969452del" "" "likely pathogenic" "" "0000128929" "0" "70" "12" "28116639" "28116639" "subst" "0" "01744" "PTHLH_000009" "g.28116639G>A" "" "{PMID:Jamsheer et al. 2016:26763883}" "" "" "" "De novo" "" "" "0" "" "" "g.27963706G>A" "" "likely pathogenic" "" "0000128935" "11" "70" "12" "28116639" "28116639" "subst" "0" "01744" "PTHLH_000009" "g.28116639G>A" "" "" "" "" "paternally inherited (healthy mosaic father)" "Germline" "" "" "0" "" "" "g.27963706G>A" "" "likely pathogenic" "" "0000128936" "11" "70" "12" "28116549" "28116549" "del" "0" "01744" "PTHLH_000008" "g.28116549del" "" "{PMID:Jamsheer et al. 2016:26763883}" "" "" "" "Germline" "yes" "" "0" "" "" "g.27963616del" "" "likely pathogenic" "" "0000132644" "21" "97" "12" "28122384" "28122384" "subst" "0" "01199" "PTHLH_000006" "g.28122384A>C" "" "{PMID:Wang 2015:25801215}" "" "" "" "Germline" "yes" "" "0" "" "" "g.27969451A>C" "" "pathogenic" "" "0000132645" "0" "97" "12" "28122384" "28122384" "subst" "0" "00006" "PTHLH_000006" "g.28122384A>C" "" "{PMID:Wang 2015:25801215}" "" "" "cDNA expression cloning in HEK293 cells shows affected signal peptide cleavage" "In vitro (cloned)" "-" "" "0" "" "" "g.27969451A>C" "" "NA" "" "0000255644" "0" "90" "12" "28122403" "28122403" "subst" "0" "01943" "PTHLH_000012" "g.28122403A>G" "" "" "" "PTHLH(NM_198966.1):c.25T>C (p.W9R)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.27969470A>G" "" "pathogenic" "" "0000306603" "0" "90" "12" "28116364" "28116364" "subst" "4.06095E-6" "01943" "PTHLH_000011" "g.28116364C>T" "" "" "" "PTHLH(NM_198966.1):c.441G>A (p.W147*)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "0" "" "" "g.27963431C>T" "" "pathogenic" "" "0000438687" "0" "77" "12" "28116706" "28116706" "subst" "0" "01744" "PTHLH_000013" "g.28116706T>C" "" "NOT DESCRIBED" "" "" "" "Unknown" "yes" "" "0" "" "" "g.27963773T>C" "" "likely pathogenic" "" "0000438688" "21" "77" "12" "28116706" "28116706" "subst" "0" "01744" "PTHLH_000013" "g.28116706T>C" "" "NOT DESCRIBED" "" "" "" "Germline" "yes" "" "0" "" "" "g.27963773T>C" "" "likely pathogenic" "" "0000818483" "0" "50" "12" "28122956" "28122956" "subst" "4.35836E-6" "03779" "PTHLH_000014" "g.28122956A>G" "" "" "" "" "" "CLASSIFICATION record" "" "rs761025088" "0" "" "" "" "" "VUS" "" "0000925612" "0" "90" "12" "28122406" "28122406" "subst" "0" "02327" "PTHLH_000015" "g.28122406G>A" "" "" "" "" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "pathogenic" "" "0000933323" "0" "50" "12" "28122956" "28122956" "subst" "4.35836E-6" "03779" "PTHLH_000014" "g.28122956A>G" "" "" "" "" "" "Unknown" "" "rs761025088" "0" "" "" "" "" "VUS" "" "0000966857" "0" "50" "12" "28116638" "28116638" "subst" "0" "02329" "PTHLH_000016" "g.28116638C>T" "" "" "" "PTHLH(NM_002820.3):c.167G>A (p.R56Q)" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "VUS" "" "0001039182" "0" "30" "12" "28116371" "28116371" "subst" "1.21827E-5" "01804" "PTHLH_000017" "g.28116371G>A" "" "" "" "PTHLH(NM_198965.2):c.434C>T (p.(Ser145Phe))" "VKGL data sharing initiative Nederland" "CLASSIFICATION record" "" "" "" "" "" "" "" "likely benign" "" ## 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 PTHLH ## Count = 21 "{{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}}" "0000096460" "00017118" "90" "-30" "0" "754" "0" "c.(?_-30)_(*220_?)del" "r.0" "p.0" "_1_5_" "0000096461" "00017118" "90" "131" "0" "131" "0" "c.131T>C" "r.(?)" "p.(Leu44Pro)" "4" "0000096462" "00017118" "90" "179" "0" "179" "0" "c.179T>C" "r.(?)" "p.(Leu60Pro)" "4" "0000096463" "00017118" "90" "358" "0" "358" "0" "c.358A>T" "r.(?)" "p.(Lys120*)" "4" "0000096464" "00017118" "90" "534" "0" "534" "0" "c.534A>G" "r.(?)" "p.(*178Trpext*53)" "5" "0000128926" "00017118" "70" "101" "3" "101" "6" "c.101+3_101+6del" "r.spl?" "p.?" "3i" "0000128928" "00017118" "70" "47" "0" "101" "73" "c.47_101+73del" "r.spl?" "p.?" "3_3i" "0000128929" "00017118" "70" "166" "0" "166" "0" "c.166C>T" "r.(?)" "p.(Arg56*)" "4" "0000128935" "00017118" "70" "166" "0" "166" "0" "c.166C>T" "r.(?)" "p.(Arg56*)" "4" "0000128936" "00017118" "70" "258" "0" "258" "0" "c.258del" "r.(?)" "p.(Asn87Thrfs*18)" "4" "0000132644" "00017118" "97" "44" "0" "44" "0" "c.44T>G" "r.(?)" "p.(Leu15Arg)" "3" "0000132645" "00017118" "97" "44" "0" "44" "0" "c.44T>G" "r.(?)" "p.Leu15Arg" "3" "0000255644" "00017118" "90" "25" "0" "25" "0" "c.25T>C" "r.(?)" "p.(Trp9Arg)" "" "0000306603" "00017118" "90" "441" "0" "441" "0" "c.441G>A" "r.(?)" "p.(Trp147Ter)" "" "0000438687" "00017118" "77" "102" "-3" "102" "-3" "c.102-3A>G" "r.spl?" "p.?" "4i" "0000438688" "00017118" "77" "102" "-3" "102" "-3" "c.102-3A>G" "r.spl?" "p.?" "4i" "0000818483" "00017118" "50" "-23" "2" "-23" "2" "c.-23+2T>C" "r.(?)" "p.(?)" "" "0000925612" "00017118" "90" "22" "0" "22" "0" "c.22C>T" "r.(?)" "p.(Gln8*)" "" "0000933323" "00017118" "50" "-23" "2" "-23" "2" "c.-23+2T>C" "r.(?)" "p.(?)" "" "0000966857" "00017118" "50" "167" "0" "167" "0" "c.167G>A" "r.(?)" "p.(Arg56Gln)" "" "0001039182" "00017118" "30" "434" "0" "434" "0" "c.434C>T" "r.(?)" "p.(Ser145Phe)" "" ## Screenings_To_Variants ## Do not remove or alter this header ## ## Count = 13 "{{screeningid}}" "{{variantid}}" "0000064824" "0000096460" "0000064825" "0000096461" "0000064826" "0000096462" "0000064827" "0000096463" "0000064828" "0000096464" "0000080050" "0000128926" "0000080052" "0000128928" "0000080053" "0000128929" "0000080058" "0000128935" "0000080059" "0000128936" "0000081937" "0000132644" "0000208738" "0000438687" "0000208739" "0000438688"