{"id":27673,"date":"2025-06-24T15:48:23","date_gmt":"2025-06-24T13:48:23","guid":{"rendered":"https:\/\/www.clinica-sante.com\/ro\/analize-fara-categorie\/panel-genetic-ciliopatii\/"},"modified":"2026-02-27T18:05:31","modified_gmt":"2026-02-27T16:05:31","slug":"panel-genetic-ciliopatii","status":"publish","type":"product","link":"https:\/\/www.clinica-sante.com\/ro\/analize-diagnostic-genetic\/panel-genetic-ciliopatii\/","title":{"rendered":"Panel genetic Ciliopatii"},"content":{"rendered":"<p><strong>Ciliopatiile<\/strong> sunt afec\u021biuni genetice rare \u0219i complexe, determinate de defecte \u00een structura sau func\u021bia cililor \u2014 organite celulare esen\u021biale pentru mi\u0219care, semnalizare \u0219i transport intracelular.<\/p>\n<\/p>\n<p>Aceste boli pot afecta rinichii, ficatul, ochii, sistemul nervos central, scheletul, pl\u0103m\u00e2nii \u0219i organele de reproducere.<\/p>\n<\/p>\n<p>Panelul genetic <strong>c<\/strong>iliopatii permite o evaluare simultan\u0103 a tuturor genelor cunoscute asociate acestor sindroame, oferind o abordare precis\u0103, rapid\u0103 \u0219i complet\u0103 a diagnosticului molecular.<\/p>\n<\/p>\n<p><strong>Afectiuni sau simptome asociate<\/strong><\/p>\n<\/p>\n<p> Ciliopatiile includ un spectru larg de sindroame \u0219i boli genetice:<\/p>\n<\/p>\n<ul>\n<li>sindrom Joubert<\/li>\n<li>sindrom Bardet-Biedl<\/li>\n<li>sindrom Alstr\u00f6m<\/li>\n<li>dischinezie ciliar\u0103 primar\u0103 (DCP)<\/li>\n<li>nefronoftiz\u0103<\/li>\n<li>boal\u0103 polichistic\u0103 renal\u0103 (ARPKD, ADPKD)<\/li>\n<li>sindrom Meckel-Gruber<\/li>\n<li>sindrom Ellis-van Creveld<\/li>\n<li>sindrom oro-facio-digital (OFD)<\/li>\n<li>ciliopatii oculare (retinopatii, distrofii de con \u0219i bastona\u0219)<\/li>\n<li>malforma\u021bii cerebrale, afectare hepatic\u0103 fibrochistic\u0103, anomalii scheletice sau de fertilitate<\/li>\n<\/ul>\n<p><strong>Cui se adreseaz\u0103<\/strong><\/p>\n<\/p>\n<p> Testul este recomandat pentru:<\/p>\n<\/p>\n<ul>\n<li>pacien\u021bi cu malforma\u021bii congenitale multiple ce sugereaz\u0103 o ciliopatie sindromic\u0103<\/li>\n<li>copii cu retard de dezvoltare, tulbur\u0103ri vizuale, renale sau respiratorii inexplicabile<\/li>\n<li>persoane cu istoric familial de boli polichistice, distrofii retiniene sau dischinezie ciliar\u0103<\/li>\n<li>cupluri cu recuren\u021b\u0103 de pierderi de sarcin\u0103 cauzate de malforma\u021bii fetale de tip ciliopatic<\/li>\n<li>medici geneticieni, pediatri, nefrologi, oftalmologi, pneumologi \u0219i neurologi implica\u021bi \u00een diagnosticul bolilor rare<\/li>\n<\/ul>\n<p><strong>Metodologie de testare<\/strong><\/p>\n<\/p>\n<p>Analiza se realizeaz\u0103 prin secven\u021biere de nou\u0103 genera\u021bie (NGS), care permite detectarea simultan\u0103 a variantelor patogene, probabil patogene \u0219i de semnifica\u021bie incert\u0103 (VUS) \u00een cele 174 de gene.<\/p>\n<p>Zonele codante \u0219i regiunile intron-exon sunt acoperite cu o acurate\u021be &gt;99%.<\/p>\n<\/p>\n<p><strong>Beneficii \u0219i importan\u021b\u0103 clinic\u0103<\/strong><\/p>\n<\/p>\n<ul>\n<li>permite identificarea cauzei genetice precise \u00een boli rare cu heterogenitate clinic\u0103 mare<\/li>\n<li>ghideaz\u0103 prognosticul, conduita terapeutic\u0103 \u0219i monitorizarea evolu\u021biei<\/li>\n<li>ofer\u0103 date pentru consiliere genetic\u0103 \u0219i testare familial\u0103 predictiv\u0103<\/li>\n<li>reduce semnificativ timpul \u0219i costul diagnosticului comparativ cu test\u0103rile genetice secven\u021biale<\/li>\n<li>faciliteaz\u0103 \u00eenrolarea pacien\u021bilor \u00een studii clinice pentru terapii genetice specifice<\/li>\n<\/ul>\n<p><strong>Particularit\u0103\u021bi \u0219i limit\u0103ri<\/strong><\/p>\n<\/p>\n<ul>\n<li>nu detecteaz\u0103 rearanjamente cromozomiale mari, expansiuni de repet\u0103ri sau variante \u00een regiuni neacoperite de NGS<\/li>\n<li>varianta VUS necesit\u0103 corelare cu fenotipul pacientului \u0219i reevaluare periodic\u0103<\/li>\n<li>testul nu stabile\u0219te severitatea clinic\u0103, ci predispozi\u021bia genetic\u0103 sau prezen\u021ba muta\u021biilor asociate<\/li>\n<\/ul>\n<p><strong>Recoltare \u0219i condi\u021bii de transport<\/strong><\/p>\n<\/p>\n<ul>\n<li>se recolteaz\u0103 s\u00e2nge venos \u00een vacutainer cu EDTA<\/li>\n<li>nu sunt necesare condi\u021bii speciale de post<\/li>\n<\/ul>\n<p><strong>Analize asociate recomandate<\/strong><\/p>\n<\/p>\n<ul>\n<li>panel renal genetic (pentru diferen\u021bierea cu alte nefropatii ereditare)<\/li>\n<li>panel genetic boli rare multisistemice<\/li>\n<li>test CFTR \u2013 pentru excluderea fibrozei chistice<\/li>\n<li>RMN cerebral, ecografie renal\u0103, evaluare oftalmologic\u0103 \u0219i auditiv\u0103<\/li>\n<li>testare familial\u0103 \u021bintit\u0103 \u00een caz de muta\u021bii identificate<\/li>\n<\/ul>\n","protected":false},"excerpt":{"rendered":"<p><strong>Panelul genetic pentru ciliopatii <\/strong>analizeaz\u0103 simultan 174 de gene implicate \u00een formarea, structura \u0219i func\u021bia cililor celulari, responsabili pentru transportul intracelular, semnalizarea \u0219i homeostazia tisular\u0103.<\/p>\n<\/p>\n<p><strong>Genele incluse:<\/strong><\/p>\n<\/p>\n<p> ADAMTS9, AHI1, AK7, ALG8, ALMS1, ANKS6, ARL13B, ARL3, ARL6, ARMC4, ARMC9, B9D1, B9D2, BBIP1, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, C11orf70, C2CD3, C8orf37, CC2D2A, CCDC103, CCDC114, CCDC151, CCDC39, CCDC40, CCDC65, CCNO, CCNQ, CELSR2, CENPF, CEP104, CEP120, CEP164, CEP19, CEP290, CEP41, CEP55, CEP83, CFAP298, CFAP410, CFTR, CLUAP1, CPLANE1, CRB2, CSPP1, CTU2, DCDC2, DDX59, DHCR7, DNAAF1, DNAAF2, DNAAF3, DNAAF4, DNAAF5, DNAH1, DNAH11, DNAH5, DNAH8, DNAH9, DNAI1, DNAI2, DNAJB11, DNAJB13, DNAL1, DRC1, DYNC2H1, DYNC2LI1, DZIP1L, EVC, EVC2, EXOC3L2, EXOC8, FAM186B, FBN3, FGFR1, FGFR2, FGFR3, GANAB, GAS8, GLIS2, HNF1B, HYLS1, ICK, IFT122, IFT140, IFT172, IFT27, IFT43, IFT52, IFT57, IFT74, IFT80, IFT81, INPP5E, INTU, INVS, IQCB1, KIAA0556, KIAA0586, KIAA0753, KIF14, KIF7, LRP5, LRRC56, LRRC6, LRRCC1, LZTFL1, MAPKBP1, MCIDAS, MKKS, MKS1, MRE11, NEK1, NEK8, NOTCH2, NPHP1, NPHP3, NPHP4, OFD1, PDE6D, PIAS1, PIBF1, PIH1D3, PKD2, PKHD1, PMM2, PRKCSH, RBM48, RCOR1, RPGR, RPGRIP1L, RSPH1, RSPH3, RSPH4A, RSPH9, SCLT1, SDCCAG8, SEC63, SLC30A7, SPAG1, SUFU, TBC1D32, TCTEX1D2, TCTN1, TCTN2, TCTN3, TMEM107, TMEM138, TMEM216, TMEM231, TMEM237, TMEM67, TRAF3IP1, TRAPPC3, TRIM32, TTC21B, TTC26, TTC8, TXNDC15, USP9X, WDPCP, WDR19, WDR34, WDR35, WDR60, XPNPEP3, ZMYND10, ZNF423.<\/p>\n","protected":false},"featured_media":0,"template":"","meta":{"_acf_changed":false,"inline_featured_image":false},"product_brand":[],"product_cat":[1209,3166,2876],"product_tag":[],"class_list":["post-27673","product","type-product","status-publish","product_cat-analize","product_cat-diagnostic-genetic","product_cat-serviciu-laborator","first","instock","sale","virtual","purchasable","product-type-simple"],"acf":[],"aioseo_notices":[],"aioseo_head":"\n\t\t<!-- All in One SEO Pro 5.0.1 - aioseo.com -->\n\t<meta name=\"description\" content=\"Panelul genetic pentru ciliopatii analizeaz\u0103 simultan 174 de gene implicate \u00een formarea, structura \u0219i func\u021bia cililor celulari, responsabili pentru transportul intracelular, semnalizarea \u0219i homeostazia tisular\u0103.Genele incluse: ADAMTS9, AHI1, AK7, ALG8, ALMS1, ANKS6, ARL13B, ARL3, ARL6, ARMC4, ARMC9, B9D1, B9D2, BBIP1, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, C11orf70, C2CD3, C8orf37, CC2D2A, CCDC103, CCDC114, CCDC151, CCDC39, CCDC40, CCDC65, CCNO, CCNQ, CELSR2, CENPF, CEP104, CEP120, CEP164, CEP19, CEP290, CEP41, CEP55, CEP83, CFAP298, CFAP410, CFTR, CLUAP1, CPLANE1, CRB2, CSPP1, CTU2, DCDC2, DDX59, DHCR7, DNAAF1, DNAAF2, DNAAF3, DNAAF4, DNAAF5, DNAH1, DNAH11, DNAH5, DNAH8, DNAH9, DNAI1, DNAI2, DNAJB11, DNAJB13, DNAL1, DRC1, DYNC2H1, DYNC2LI1, DZIP1L, EVC, EVC2, EXOC3L2, EXOC8, FAM186B, FBN3, FGFR1, FGFR2, FGFR3, GANAB, GAS8, GLIS2, HNF1B, HYLS1, ICK, IFT122, IFT140, IFT172, IFT27, IFT43, IFT52, IFT57, IFT74, IFT80, IFT81, INPP5E, INTU, INVS, IQCB1, KIAA0556, KIAA0586, KIAA0753, KIF14, KIF7, LRP5, LRRC56, LRRC6, LRRCC1, LZTFL1, MAPKBP1, MCIDAS, MKKS, MKS1, MRE11, NEK1, NEK8, NOTCH2, NPHP1, NPHP3, NPHP4, OFD1, PDE6D, PIAS1, PIBF1, PIH1D3, PKD2, PKHD1, PMM2, PRKCSH, RBM48, RCOR1, RPGR, RPGRIP1L, RSPH1, RSPH3, RSPH4A, RSPH9, SCLT1, SDCCAG8, SEC63, SLC30A7, SPAG1, SUFU, TBC1D32, TCTEX1D2, TCTN1, TCTN2, TCTN3, TMEM107, TMEM138, TMEM216, TMEM231, TMEM237, TMEM67, TRAF3IP1, TRAPPC3, TRIM32, TTC21B, TTC26, TTC8, TXNDC15, USP9X, WDPCP, WDR19, WDR34, WDR35, WDR60, XPNPEP3, ZMYND10, ZNF423.\" \/>\n\t<meta name=\"robots\" content=\"max-image-preview:large\" \/>\n\t<link rel=\"canonical\" href=\"https:\/\/www.clinica-sante.com\/ro\/analize-diagnostic-genetic\/panel-genetic-ciliopatii\/\" \/>\n\t<meta name=\"generator\" content=\"All in One SEO Pro (AIOSEO) 5.0.1\" \/>\n\t\t<meta property=\"og:locale\" content=\"ro_RO\" \/>\n\t\t<meta property=\"og:site_name\" content=\"Clinica Sante - Laborator de Analize Medicale - Clinica Sante - Laborator de Analize Medicale\" \/>\n\t\t<meta property=\"og:type\" content=\"article\" \/>\n\t\t<meta property=\"og:title\" content=\"Panel genetic Ciliopatii - Clinica Sante - Laborator de Analize Medicale\" \/>\n\t\t<meta property=\"og:description\" content=\"Panelul genetic pentru ciliopatii analizeaz\u0103 simultan 174 de gene implicate \u00een formarea, structura \u0219i func\u021bia cililor celulari, responsabili pentru transportul intracelular, semnalizarea \u0219i homeostazia tisular\u0103.Genele incluse: ADAMTS9, AHI1, AK7, ALG8, ALMS1, ANKS6, ARL13B, ARL3, ARL6, ARMC4, ARMC9, B9D1, B9D2, BBIP1, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, C11orf70, C2CD3, C8orf37, CC2D2A, CCDC103, CCDC114, CCDC151, CCDC39, CCDC40, CCDC65, CCNO, CCNQ, CELSR2, CENPF, CEP104, CEP120, CEP164, CEP19, CEP290, CEP41, CEP55, CEP83, CFAP298, CFAP410, CFTR, CLUAP1, CPLANE1, CRB2, CSPP1, CTU2, DCDC2, DDX59, DHCR7, DNAAF1, DNAAF2, DNAAF3, DNAAF4, DNAAF5, DNAH1, DNAH11, DNAH5, DNAH8, DNAH9, DNAI1, DNAI2, DNAJB11, DNAJB13, DNAL1, DRC1, DYNC2H1, DYNC2LI1, DZIP1L, EVC, EVC2, EXOC3L2, EXOC8, FAM186B, FBN3, FGFR1, FGFR2, FGFR3, GANAB, GAS8, GLIS2, HNF1B, HYLS1, ICK, IFT122, IFT140, IFT172, IFT27, IFT43, IFT52, IFT57, IFT74, IFT80, IFT81, INPP5E, INTU, INVS, IQCB1, KIAA0556, KIAA0586, KIAA0753, KIF14, KIF7, LRP5, LRRC56, LRRC6, LRRCC1, LZTFL1, MAPKBP1, MCIDAS, MKKS, MKS1, MRE11, NEK1, NEK8, NOTCH2, NPHP1, NPHP3, NPHP4, OFD1, PDE6D, PIAS1, PIBF1, PIH1D3, PKD2, PKHD1, PMM2, PRKCSH, RBM48, RCOR1, RPGR, RPGRIP1L, RSPH1, RSPH3, RSPH4A, RSPH9, SCLT1, SDCCAG8, SEC63, SLC30A7, SPAG1, SUFU, TBC1D32, TCTEX1D2, TCTN1, TCTN2, TCTN3, TMEM107, TMEM138, TMEM216, TMEM231, TMEM237, TMEM67, TRAF3IP1, TRAPPC3, TRIM32, TTC21B, TTC26, TTC8, TXNDC15, USP9X, WDPCP, WDR19, WDR34, WDR35, WDR60, XPNPEP3, ZMYND10, ZNF423.\" \/>\n\t\t<meta property=\"og:url\" content=\"https:\/\/www.clinica-sante.com\/ro\/analize-diagnostic-genetic\/panel-genetic-ciliopatii\/\" \/>\n\t\t<meta property=\"article:published_time\" content=\"2025-06-24T13:48:23+00:00\" \/>\n\t\t<meta property=\"article:modified_time\" content=\"2026-02-27T16:05:31+00:00\" \/>\n\t\t<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n\t\t<meta name=\"twitter:title\" content=\"Panel genetic Ciliopatii - Clinica Sante - Laborator de Analize Medicale\" \/>\n\t\t<meta name=\"twitter:description\" content=\"Panelul genetic pentru ciliopatii analizeaz\u0103 simultan 174 de gene implicate \u00een formarea, structura \u0219i func\u021bia cililor celulari, responsabili pentru transportul intracelular, semnalizarea \u0219i homeostazia tisular\u0103.Genele incluse: ADAMTS9, AHI1, AK7, ALG8, ALMS1, ANKS6, ARL13B, ARL3, ARL6, ARMC4, ARMC9, B9D1, B9D2, BBIP1, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, C11orf70, C2CD3, C8orf37, CC2D2A, CCDC103, CCDC114, CCDC151, CCDC39, CCDC40, CCDC65, CCNO, CCNQ, CELSR2, CENPF, CEP104, CEP120, CEP164, CEP19, CEP290, CEP41, CEP55, CEP83, CFAP298, CFAP410, CFTR, CLUAP1, CPLANE1, CRB2, CSPP1, CTU2, DCDC2, DDX59, DHCR7, DNAAF1, DNAAF2, DNAAF3, DNAAF4, DNAAF5, DNAH1, DNAH11, DNAH5, DNAH8, DNAH9, DNAI1, DNAI2, DNAJB11, DNAJB13, DNAL1, DRC1, DYNC2H1, DYNC2LI1, DZIP1L, EVC, EVC2, EXOC3L2, EXOC8, FAM186B, FBN3, FGFR1, FGFR2, FGFR3, GANAB, GAS8, GLIS2, HNF1B, HYLS1, ICK, IFT122, IFT140, IFT172, IFT27, IFT43, IFT52, IFT57, IFT74, IFT80, IFT81, INPP5E, INTU, INVS, IQCB1, KIAA0556, KIAA0586, KIAA0753, KIF14, KIF7, LRP5, LRRC56, LRRC6, LRRCC1, LZTFL1, MAPKBP1, MCIDAS, MKKS, MKS1, MRE11, NEK1, NEK8, NOTCH2, NPHP1, NPHP3, NPHP4, OFD1, PDE6D, PIAS1, PIBF1, PIH1D3, PKD2, PKHD1, PMM2, PRKCSH, RBM48, RCOR1, RPGR, RPGRIP1L, RSPH1, RSPH3, RSPH4A, RSPH9, SCLT1, SDCCAG8, SEC63, SLC30A7, SPAG1, SUFU, TBC1D32, TCTEX1D2, TCTN1, TCTN2, TCTN3, TMEM107, TMEM138, TMEM216, TMEM231, TMEM237, TMEM67, TRAF3IP1, TRAPPC3, TRIM32, TTC21B, TTC26, TTC8, TXNDC15, USP9X, WDPCP, WDR19, WDR34, WDR35, WDR60, XPNPEP3, ZMYND10, ZNF423.\" \/>\n\t\t<script type=\"application\/ld+json\" class=\"aioseo-schema\">\n\t\t\t{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\\\/\\\/www.clinica-sante.com\\\/ro\\\/analize-diagnostic-genetic\\\/panel-genetic-ciliopatii\\\/#breadcrumblist\",\"itemListElement\":[{\"@type\":\"ListItem\",\"@id\":\"https:\\\/\\\/www.clinica-sante.com\\\/ro#listItem\",\"position\":1,\"name\":\"Prima 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CTU2, DCDC2, DDX59, DHCR7, DNAAF1, DNAAF2, DNAAF3, DNAAF4, DNAAF5, DNAH1, DNAH11, DNAH5, DNAH8, DNAH9, DNAI1, DNAI2, DNAJB11, DNAJB13, DNAL1, DRC1, DYNC2H1, DYNC2LI1, DZIP1L, EVC, EVC2, EXOC3L2, EXOC8, FAM186B, FBN3, FGFR1, FGFR2, FGFR3, GANAB, GAS8, GLIS2, HNF1B, HYLS1, ICK, IFT122, IFT140, IFT172, IFT27, IFT43, IFT52, IFT57, IFT74, IFT80, IFT81, INPP5E, INTU, INVS, IQCB1, KIAA0556, KIAA0586, KIAA0753, KIF14, KIF7, LRP5, LRRC56, LRRC6, LRRCC1, LZTFL1, MAPKBP1, MCIDAS, MKKS, MKS1, MRE11, NEK1, NEK8, NOTCH2, NPHP1, NPHP3, NPHP4, OFD1, PDE6D, PIAS1, PIBF1, PIH1D3, PKD2, PKHD1, PMM2, PRKCSH, RBM48, RCOR1, RPGR, RPGRIP1L, RSPH1, RSPH3, RSPH4A, RSPH9, SCLT1, SDCCAG8, SEC63, SLC30A7, SPAG1, SUFU, TBC1D32, TCTEX1D2, TCTN1, TCTN2, TCTN3, TMEM107, TMEM138, TMEM216, TMEM231, TMEM237, TMEM67, TRAF3IP1, TRAPPC3, TRIM32, TTC21B, TTC26, TTC8, TXNDC15, USP9X, WDPCP, WDR19, WDR34, WDR35, WDR60, XPNPEP3, ZMYND10, ZNF423.","og:url":"https:\/\/www.clinica-sante.com\/ro\/analize-diagnostic-genetic\/panel-genetic-ciliopatii\/","article:published_time":"2025-06-24T13:48:23+00:00","article:modified_time":"2026-02-27T16:05:31+00:00","twitter:card":"summary_large_image","twitter:title":"Panel genetic Ciliopatii - Clinica Sante - Laborator de Analize Medicale","twitter:description":"Panelul genetic pentru ciliopatii analizeaz\u0103 simultan 174 de gene implicate \u00een formarea, structura \u0219i func\u021bia cililor celulari, responsabili pentru transportul intracelular, semnalizarea \u0219i homeostazia tisular\u0103.Genele incluse: ADAMTS9, AHI1, AK7, ALG8, ALMS1, ANKS6, ARL13B, ARL3, ARL6, ARMC4, ARMC9, B9D1, B9D2, BBIP1, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, C11orf70, C2CD3, C8orf37, CC2D2A, CCDC103, CCDC114, CCDC151, CCDC39, CCDC40, CCDC65, CCNO, CCNQ, CELSR2, CENPF, CEP104, CEP120, CEP164, CEP19, CEP290, CEP41, CEP55, CEP83, CFAP298, CFAP410, CFTR, CLUAP1, CPLANE1, CRB2, CSPP1, CTU2, DCDC2, DDX59, DHCR7, DNAAF1, DNAAF2, DNAAF3, DNAAF4, DNAAF5, DNAH1, DNAH11, DNAH5, DNAH8, DNAH9, DNAI1, DNAI2, DNAJB11, DNAJB13, DNAL1, DRC1, DYNC2H1, DYNC2LI1, DZIP1L, EVC, EVC2, EXOC3L2, EXOC8, FAM186B, FBN3, FGFR1, FGFR2, FGFR3, GANAB, GAS8, GLIS2, HNF1B, HYLS1, ICK, IFT122, IFT140, IFT172, IFT27, IFT43, IFT52, IFT57, IFT74, IFT80, IFT81, INPP5E, INTU, INVS, IQCB1, KIAA0556, KIAA0586, KIAA0753, KIF14, KIF7, LRP5, LRRC56, LRRC6, LRRCC1, LZTFL1, MAPKBP1, MCIDAS, MKKS, MKS1, MRE11, NEK1, NEK8, NOTCH2, NPHP1, NPHP3, NPHP4, OFD1, PDE6D, PIAS1, PIBF1, PIH1D3, PKD2, PKHD1, PMM2, PRKCSH, RBM48, RCOR1, RPGR, RPGRIP1L, RSPH1, RSPH3, RSPH4A, RSPH9, SCLT1, SDCCAG8, SEC63, SLC30A7, SPAG1, SUFU, TBC1D32, TCTEX1D2, TCTN1, TCTN2, TCTN3, TMEM107, TMEM138, TMEM216, TMEM231, TMEM237, TMEM67, TRAF3IP1, TRAPPC3, TRIM32, TTC21B, TTC26, TTC8, TXNDC15, USP9X, WDPCP, WDR19, WDR34, WDR35, WDR60, XPNPEP3, ZMYND10, ZNF423."},"aioseo_meta_data":{"post_id":"27673","title":null,"description":null,"keywords":null,"keyphrases":{"focus":[],"additional":[]},"primary_term":null,"canonical_url":null,"og_title":null,"og_description":null,"og_object_type":"default","og_image_type":"default","og_image_url":null,"og_image_width":null,"og_image_height":null,"og_image_custom_url":null,"og_image_custom_fields":null,"og_video":null,"og_custom_url":null,"og_article_section":null,"og_article_tags":null,"twitter_use_og":false,"twitter_card":"default","twitter_image_type":"default","twitter_image_url":null,"twitter_image_custom_url":null,"twitter_image_custom_fields":null,"twitter_title":null,"twitter_description":null,"schema":{"blockGraphs":[],"customGraphs":[],"default":{"data":{"Article":[],"Course":[],"Dataset":[],"FAQPage":[],"Movie":[],"Person":[],"Product":[],"ProductReview":[],"Car":[],"Recipe":[],"Service":[],"SoftwareApplication":[],"WebPage":[]},"graphName":"","isEnabled":true},"graphs":[]},"schema_type":"default","schema_type_options":null,"pillar_content":false,"robots_default":true,"robots_noindex":false,"robots_noarchive":false,"robots_nosnippet":false,"robots_nofollow":false,"robots_noimageindex":false,"robots_noodp":false,"robots_notranslate":false,"robots_max_snippet":null,"robots_max_videopreview":null,"robots_max_imagepreview":"large","priority":null,"frequency":null,"local_seo":null,"seo_analyzer_scan_date":"2026-05-25 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