Ciliopathies gene panel dg216

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CILIOPATHIES GENE PANEL DG 2.16 (151 genes) Releasedate: 07-06-2019 Gene ADAMTS9 AHI1 ALMS1 ANKS6 ARL13B ARL6Median coverage 115,7 129,8 172,8 94,2 102,2 100,3%…
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CILIOPATHIES GENE PANEL DG 2.16 (151 genes) Releasedate: 07-06-2019 Gene ADAMTS9 AHI1 ALMS1 ANKS6 ARL13B ARL6Median coverage 115,7 129,8 172,8 94,2 102,2 100,3% covered > 10x 99.5% 99.7% 100.0% 98.3% 100.0% 99.8%% covered > 20x 97.4% 98.3% 99.7% 94.4% 99.4% 98.2%ARMC4 ARMC9 B9D1107,2 94.4% 124,8 100.0% 103,7 92.2%93.5% 99.3% 92.1%B9D2105,8 100.0%100.0%BBIP1 BBS1 BBS10 BBS12 BBS2119,7 146,4 158,1 187,1 150,797.3% 100.0% 100.0% 100.0% 99.9%90.3% 100.0% 99.9% 100.0% 99.6%BBS4 BBS5 BBS7 BBS9 C11orf70 C21orf2110,2 98,5 142,9 113,699.9% 98.0% 99.1% 98.6% NC NC99.2% 93.3% 96.5% 94.4% NC NCNC 116,9 95.8%NC 95.2%C21orf59 C2CD3NC NC NCAssociated Phenotype description and OMIM disease ID No OMIM phenotype Joubert syndrome 3, 608629 Alstrom syndrome, 203800 Nephronophthisis 16, 615382 Joubert syndrome 8, 612291 ?Retinitis pigmentosa 55, 613575 Bardet-Biedl syndrome 3, 600151 {Bardet-Biedl syndrome 1, modifier of}, 209900 Ciliary dyskinesia, primary, 23, 615451 Joubert syndrome 30, 617622 ?Meckel syndrome 9, 614209 Joubert syndrome 27, 617120 ?Meckel syndrome 10, 614175 Joubert syndrome 34, 614175 ?Bardet-Biedl syndrome 18, 615995 Bardet-Biedl syndrome 1, 209900 Bardet-Biedl syndrome 10, 615987 Bardet-Biedl syndrome 12, 615989 Bardet-Biedl syndrome 2, 615981 Retinitis pigmentosa 74, 616562 Bardet-Biedl syndrome 4, 615982 Bardet-Biedl syndrome 5, 615983 Bardet-Biedl syndrome 7, 615984 Bardet-Biedl syndrome 9, 615986 Ciliary dyskinesia, primary, 38, 618063 Retinal dystrophy with macular staphyloma, 617547 Spondylometaphyseal dysplasia, axial, 602271 Ciliary dyskinesia, primary, 26, 615500 Orofaciodigital syndrome XIV, 615948C5orf42NCNCNCC8orf37144,1 99.8%99.4%CC2D2A111,7 99.0%97.1%CCDC103 CCDC114 CCDC151 CCDC28B CCDC39 CCDC40 CCDC65 CCNO CENPF CEP104 CEP120116,2 134,1 127,2 84,3 86,7 112 80,3 130,9 139,9 104 131,799.8% 99.8% 100.0% 98.5% 96.8% 98.4% 97.1% 99.8% 98.7% 97.5% 99.4%CEP164 CEP290100.0% 100.0% 100.0% 100.0% 99.4% 99.4% 99.6% 100.0% 99.8% 99.3% 100.0%89,3 99.8% 82,6 97.3%CEP41 CEP55 CEP83 CSPP1 DCDC278,2 124,5 108,8 119 15098.9% 100.0% 99.4% 100.0% 99.9%DDX59 DNAAF1 DNAAF2141,5 100.0% 112,8 100.0% 150,1 99.9%98.0% 91.7%94.4% 100.0% 96.6% 99.1% 99.8%99.8% 99.5% 98.7%Joubert syndrome 17, 614615 Orofaciodigital syndrome VI, 277170 Bardet-Biedl syndrome 21, 617406 Cone-rod dystrophy 16, 614500 Retinitis pigmentosa 64, 614500 COACH syndrome, 216360 Joubert syndrome 9, 612285 Meckel syndrome 6, 612284 Ciliary dyskinesia, primary, 17, 614679 Ciliary dyskinesia, primary, 20, 615067 Ciliary dyskinesia, primary, 30, 616037 {Bardet-Biedl syndrome 1, modifier of}, 209900 Ciliary dyskinesia, primary, 14, 613807 Ciliary dyskinesia, primary, 15, 613808 Ciliary dyskinesia, primary, 27, 615504 Ciliary dyskinesia, primary, 29, 615872 Stromme syndrome, 243605 Joubert syndrome 25, 616781 Joubert syndrome 31, 617761 Short-rib thoracic dysplasia 13 with or without polydactyly, 616300 Nephronophthisis 15, 614845 ?Bardet-Biedl syndrome 14, 615991 Joubert syndrome 5, 610188 Leber congenital amaurosis 10, 611755 Meckel syndrome 4, 611134 Senior-Loken syndrome 6, 610189 Joubert syndrome 15, 614464 Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly, 236500 Nephronophthisis 18, 615862 Joubert syndrome 21, 615636 ?Deafness, autosomal recessive 66, 610212 Nephronophthisis 19, 616217 Sclerosing cholangitis, neonatal, 617394 Orofaciodigital syndrome V, 174300 Ciliary dyskinesia, primary, 13, 613193 Ciliary dyskinesia, primary, 10, 612518DNAAF3 DNAAF4115 99.9% 94,1 99.9%98.5% 98.2%DNAAF5 DNAH1107,6 95.4% 158,1 100.0%85.2% 99.8%DNAH11 DNAH17131,3 99.8% 126 100.0%98.7% 99.6%DNAH5 DNAI1 DNAI2 DNAJB13 DNAL1 DNHD1114,1 115,4 151,7 116,3 104 148,399.9% 100.0% 99.6% 100.0% 99.3% 100.0%99.1% 100.0% 96.6% 99.5% 96.2% 99.9%DRC1 DYNC2H1 DYNC2LI1 EVC91,2 102,2 95,4 106,3100.0% 98.8% 99.7% 95.9%99.3% 95.5% 97.0% 92.4%EVC2110,2 99.4%96.3%EXOC8152,6 100.0%100.0%EXTL3 FUZ GAS8 GLIS2 HYDIN HYLS1 IFT122 IFT140184,1 128,5 127,3 129,6 106,8 156,6 120,5 117,6100.0% 100.0% 99.4% 100.0% 98.9% 100.0% 99.0% 99.2%IFT172100.0% 100.0% 100.0% 100.0% 99.8% 100.0% 99.9% 99.9%94,5 100.0%99.4%Ciliary dyskinesia, primary, 2, 606763 Ciliary dyskinesia, primary, 25, 615482 {Dyslexia, susceptibility to, 1}, 127700 Ciliary dyskinesia, primary, 18, 614874 ?Ciliary dyskinesia, primary, 37, 617577 Spermatogenic failure 18, 617576 Ciliary dyskinesia, primary, 7, with or without situs inversus, 611884 No OMIM phenotype ?Lung hypoplasia, polycystic kidneys and hypertrophy of the heart (Yates (2017) Genet Med 19,1171) Ciliary dyskinesia, primary, 3, with or without situs inversus, 608644 Ciliary dyskinesia, primary, 1, with or without situs inversus, 244400 Ciliary dyskinesia, primary, 9, with or without situs inversus, 612444 Ciliary dyskinesia, primary, 34, 617091 Ciliary dyskinesia, primary, 16, 614017 No OMIM phenotype ?Diabetic retinopathy (Ung (2017) Vision Res epub) ?Global developmental delay (Anazi (2016) Mol Psychiatry epub,epub) Ciliary dyskinesia, primary, 21, 615294 Short-rib thoracic dysplasia 3 with or without polydactyly, 613091 Short-rib thoracic dysplasia 15 with polydactyly, 617088 ?Weyers acrofacial dysostosis, 193530 Ellis-van Creveld syndrome, 225500 Ellis-van Creveld syndrome, 225500 Weyers acrofacial dysostosis, 193530 No OMIM phenotype Joubert syndrome (Dixon-Salazar (2012) Sci Transl Med 4, 138ra78) Immunoskeletal dysplasia with neurodevelopmental abnormalities, 617425 {Neural tube defects, susceptibility to}, 182940 Ciliary dyskinesia, primary, 33, 616726 Nephronophthisis 7, 611498 Ciliary dyskinesia, primary, 5, 608647 Hydrolethalus syndrome, 236680 Cranioectodermal dysplasia 1, 218330 Retinitis pigmentosa 80, 617781 Short-rib thoracic dysplasia 9 with or without polydactyly, 266920 Retinitis pigmentosa 71, 616394IFT27 IFT43115,8 100.0% 112,4 100.0%100.0% 100.0%IFT52 IFT80 IFT81 INPP5E121 64,9 92,3 116,899.7% 84.7% 89.0% 98.6%INTU115,4 99.8%98.7%INVS IQCB1 KCTD3143,7 100.0% 93,3 91.6% 129,3 99.9%99.9% 80.0% 99.5%KIAA0556 KIAA0586126,6 100.0% 117,7 97.0%99.6% 93.0%KIAA0753 KIF14113,2 99.9% 116,6 99.6%98.7% 97.9%KIF7105,2 98.2%93.5%LBR103 98.3%91.5%LCA5 LRRC56 LRRC6 LZTFL1 MAPKBP1 MKKS139,9 130,7 139,3 117 132,5 155,7100.0% 96.7% 93.6% 100.0%99.8% 100.0% 99.8% 99.8% 100.0% 83.2%98.9% 99.2% 97.3% 99.2% 100.0% 83.2%Short-rib thoracic dysplasia 10 with or without polydactyly, 615630 ?Bardet-Biedl syndrome 19, 615996 ?Cranioectodermal dysplasia 3, 614099 ?Retinitis pigmentosa 81, 617871 Short-rib thoracic dysplasia 18 with polydactyly, 617866 Short-rib thoracic dysplasia 16 with or without polydactyly, 617102 Short-rib thoracic dysplasia 2 with or without polydactyly, 611263 Short-rib thoracic dysplasia 19 with or without polydactyly, 617895 Joubert syndrome 1, 213300 Mental retardation, truncal obesity, retinal dystrophy, and micropenis, 610156 ?Orofaciodigital syndrome XVII, 617926 ?Short-rib thoracic dysplasia 20 with polydactyly, 617925 Nephronophthisis 2, infantile, 602088 Senior-Loken syndrome 5, 609254 No OMIM phenotype Ciliopathy and Joubert syndrome (Alfares (2017) Mol Genet Metab 121,91) Severe psychomotor retardation, seizure and cerebellar hypoplasia (Alazami (2015) Cell Rep 10,148) Joubert syndrome 26, 616784 Joubert syndrome 23, 616490 Short-rib thoracic dysplasia 14 with polydactyly, 616546 ?Orofaciodigital syndrome XV, 617127 ?Meckel syndrome 12, 616258 Microcephaly 20, primary, autosomal recessive, 617914 ?Al-Gazali-Bakalinova syndrome, 607131 ?Hydrolethalus syndrome 2, 614120 Acrocallosal syndrome, 200990 Joubert syndrome 12, 200990 ?Reynolds syndrome, 613471 Greenberg skeletal dysplasia, 215140 Pelger-Huet anomaly, 169400 Pelger-Huet anomaly with mild skeletal anomalies, 618019 Leber congenital amaurosis 5, 604537 Ciliary dyskinesia, primary, 39, 618254 Ciliary dyskinesia, primary, 19, 614935 Bardet-Biedl syndrome 17, 615994 Nephronophthisis 20, 617271 Bardet-Biedl syndrome 6, 605231MKS192,4 99.6%97.8%NCAPG2 NEK1121,5 99.8% 115,9 99.7%98.2% 98.1%NEK8141,3 100.0%99.9%NME8 NPHP1104,7 98.6% 121,2 99.8%93.8% 98.5%NPHP3121,4 99.8%98.5%NPHP4125,6 100.0%99.7%OCRL106,2 99.8%98.3%OFD151,9 85.8%70.8%PDE6D PIBF1 PIH1D3 PKD1 PKD2 PKHD1 POC1A RPGRIP1L114,7 74,3 74,7 35,9 102,3 130,4 112,9 123,4100.0% 99.2% 98.4% 43.0% 98.7% 99.9% 100.0% 96.7%RSPH1 RSPH3 RSPH4A122,6 100.0% 139,5 99.9% 146,9 98.1%99.9% 94.4% 89.1% 35.0% 95.8% 99.4% 100.0% 95.4%99.9% 99.3% 95.3%McKusick-Kaufman syndrome, 236700 Bardet-Biedl syndrome 13, 615990 Joubert syndrome 28, 617121 Meckel syndrome 1, 249000 No OMIM phenotype Short-rib thoracic dysplasia 6 with or without polydactyly, 263520 {Amyotrophic lateral sclerosis, susceptibility to, 24}, 617892 ?Nephronophthisis 9, 613824 Renal-hepatic-pancreatic dysplasia 2, 615415 Ciliary dyskinesia, primary, 6, 610852 Joubert syndrome 4, 609583 Nephronophthisis 1, juvenile, 256100 Senior-Loken syndrome-1, 266900 Meckel syndrome 7, 267010 Nephronophthisis 3, 604387 Renal-hepatic-pancreatic dysplasia 1, 208540 Nephronophthisis 4, 606966 Senior-Loken syndrome 4, 606996 Dent disease 2, 300555 Lowe syndrome, 309000 ?Retinitis pigmentosa 23, 300424 Joubert syndrome 10, 300804 Orofaciodigital syndrome I, 311200 Simpson-Golabi-Behmel syndrome, type 2, 300209 ?Joubert syndrome 22, 615665 Joubert syndrome 33, 617767 Ciliary dyskinesia, primary, 36, X-linked, 300991 Polycystic kidney disease 1, 173900 Polycystic kidney disease 2, 613095 Polycystic kidney disease 4, with or without hepatic disease, 263200 Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis, 614813 COACH syndrome, 216360 Joubert syndrome 7, 611560 Meckel syndrome 5, 611561 Ciliary dyskinesia, primary, 24, 615481 Ciliary dyskinesia, primary, 32, 616481 Ciliary dyskinesia, primary, 11, 612649RSPH9 SCLT1131,2 99.7% 90,3 95.8%97.1% 90.8%SDCCAG8124,1 100.0%99.7%SPAG1 SPATA7101,6 99.1% 122,7 99.4%95.3% 97.4%TBC1D3295,5 99.4%96.5%TCTEX1D2 TCTN1 TCTN2123,6 100.0% 94,8 95.6% 122,4 99.9%99.4% 92.3% 99.0%TCTN3116,3 100.0%99.9%TMEM107148,7 100.0%100.0%TMEM138 TMEM21682,7 100.0% 88 99.7%99.2% 95.7%TMEM231101,1 100.0%99.3%TMEM237 TMEM260 TMEM67117,7 100.0% 117,5 99.6% 83,1 99.1%99.2% 97.6% 94.6%TRAF3IP1 TRIM3284,2 99.4% 123 100.0%97.1% 100.0%TTBK2 TTC21B108,4 99.9% 119,5 99.7%96.8% 98.8%Ciliary dyskinesia, primary, 12, 612650 No OMIM phenotype Oro-facio-digital syndrome type IX (Adly (2014) Hum Mutat 35,36) Bardet-Biedl syndrome 16, 615993 Senior-Loken syndrome 7, 613615 Ciliary dyskinesia, primary, 28, 615505 Leber congenital amaurosis 3, 604232 Retinitis pigmentosa, juvenile, autosomal recessive, 604232 No OMIM phenotype Oro-facio-digital syndrome type IX (Adly (2014) Hum Mutat 35, 36) Short-rib thoracic dysplasia 17 with or without polydactyly, 617405 Joubert syndrome 13, 614173 ?Meckel syndrome 8, 613885 Joubert syndrome 24, 616654 Joubert syndrome 18, 614815 Orofaciodigital syndrome IV, 258860 ?Joubert syndrome 29, 617562 Meckel syndrome 13, 617562 Orofaciodigital syndrome XVI, 617563 Joubert syndrome 16, 614465 Joubert syndrome 2, 608091 Meckel syndrome 2, 603194 Joubert syndrome 20, 614970 Meckel syndrome 11, 615397 Joubert syndrome 14, 614424 Structural heart defects and renal anomalies syndrome, 617478 ?RHYNS syndrome, 602152 COACH syndrome, 216360 Joubert syndrome 6, 610688 Meckel syndrome 3, 607361 Nephronophthisis 11, 613550 {Bardet-Biedl syndrome 14, modifier of}, 615991 Senior-Loken syndrome 9, 616629 ?Bardet-Biedl syndrome 11, 615988 Muscular dystrophy, limb-girdle, autosomal recessive 8, 254110 Spinocerebellar ataxia 11, 604432 Nephronophthisis 12, 613820TTC25 TTC26 TTC893,7 100.0% 140,5 99.8% 115,2 99.8%99.6% 99.2% 98.8%TULP1117,9 100.0%99.6%VHL169,6 100.0%98.3%WDPCP106,7 97.8%94.9%WDR19126,8 100.0%99.2%WDR34 WDR35116,1 100.0% 141,8 99.7%100.0% 98.4%WDR60 XPNPEP3 ZMYND10 ZNF423108,1 99,9 123 192,998.1% 99.4% 100.0% 100.0%99.7% 100.0% 100.0% 100.0%Short-rib thoracic dysplasia 4 with or without polydactyly, 613819 Ciliary dyskinesia, primary, 35, 617092 No OMIM phenotype ?Retinitis pigmentosa 51, 613464 Bardet-Biedl syndrome 8, 615985 Leber congenital amaurosis 15, 613843 Retinitis pigmentosa 14, 600132 Erythrocytosis, familial, 2, 263400 Hemangioblastoma, cerebellar, somatic, 0 Pheochromocytoma, 171300 Renal cell carcinoma, somatic, 144700 von Hippel-Lindau syndrome, 193300 ?Bardet-Biedl syndrome 15, 615992 ?Congenital heart defects, hamartomas of tongue, and polysyndactyly, 217085 ?Cranioectodermal dysplasia 4, 614378 ?Short-rib thoracic dysplasia 5 with or without polydactyly, 614376 Nephronophthisis 13, 614377 Senior-Loken syndrome 8, 616307 Short-rib thoracic dysplasia 11 with or without polydactyly, 615633 Cranioectodermal dysplasia 2, 613610 Short-rib thoracic dysplasia 7 with or without polydactyly, 614091 Short-rib thoracic dysplasia 8 with or without polydactyly, 615503 Nephronophthisis-like nephropathy 1, 613159 Ciliary dyskinesia, primary, 22, 615444 Joubert syndrome 19, 614844 Nephronophthisis 14, 614844Gene symbols used follow HGCN guidelines: Gray KA, Yates B, Seal RL, Wright MW, Bruford EA. Nucleic Acids Res. 2015 Jan;43(Database issue):D1079-85. Median Coverage describes the average number of reads seen across 50 exomes. % Covered 10x describes the percentage of a gene’s coding sequence that is covered at least 10x. % Covered 20x describes the percentage of a gene’s coding sequence that is covered at least 20x. Genes with Median Coverage and % Covered 10x/20x denoting NC are non-coding genes for which coverage statistics could not be generated. OMIM release used for OMIM disease identifiers and descriptions : May 8th, 2019. This list is accurate for panel version DG 2.16 Ad 1. “No OMIM phenotype” signifies a gene without a current OMIM association Ad 2. OMIM phenotype descriptions between {} signify risk factors
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