- Analytes
- DSC2
DSC2
Name: |
desmocollin 2
|
Symbol: |
DSC2
|
Version of Orphanet: |
2023-06-22 14:14:43
|
Synonyms: |
CDHF2
|
XREF(s): | |
Created: |
13 May 2019 - 01:01
|
Changed: |
22 Jun 2023 - 16:14
|
- Arrhytmogenic cardiopathy
- Cardiomyopathy: hypertrophic cardiomyopathy, dilated cardiomyopathy, restrictive cardiomyopathy, left ventricular non-compaction cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy (gene panel)
- Dilated Cardiomyopathy (Gene panel)
- Primary Electrical disorders / Brugada syndrome / Long QT syndrome (LQT) / Short QT syndrome (SQT) / Arrhythmogenic right ventricular cardiomyopathy (ARVC) / Catecholaminergic polymorphic ventricular tachycardia (CPVT) (gene panel)
-
Arrhytmogenic cardiopathy - UGent
Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments DES 100.00 1 DSC2 100.00 1 DSG2 100.00 1 DSP 100.00 1 JUP 100.00 1 PKP2 100.00 1 PLN 100.00 1 TMEM43 100.00 1 -
Cardiomyopathy (genepanel) - UZA
Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments ABCC9 100.00 0 ACTC1 100.00 0 ACTN2 100.00 0 ANKRD1 100.00 0 BAG3 100.00 0 CAV3 100.00 0 CRYAB 100.00 0 CSRP3 100.00 0 CTNNA3 100.00 0 DES 100.00 0 DSC2 100.00 0 DSG2 100.00 0 DSP 100.00 0 EMD 100.00 0 FHL1 100.00 0 GLA 100.00 0 JUP 100.00 0 LAMA4 100.00 0 LAMP2 100.00 0 LDB3 100.00 0 LMNA 100.00 0 MIB1 100.00 0 MYBPC3 100.00 0 MYH6 98.00 0 MYH7 100.00 0 MYL2 100.00 0 NEXN 100.00 0 PKP2 100.00 0 PLN 100.00 0 PRDM16 100.00 0 PRKAG2 100.00 0 RBM20 100.00 0 SCN5A 100.00 0 SGCD 99.00 0 TAFAZZIN 100.00 0 TCAP 100.00 0 TGFB3 100.00 0 TMEM43 100.00 0 TNNC1 100.00 0 TNNI3 100.00 0 TNNT2 100.00 0 TPM1 100.00 0 TTN 100.00 0 TTR 100.00 0 VCL 100.00 0 RYR2 100.00 0 FLNC 100.00 0 FHL2 100.00 0 NEBL 100.00 0 RAF1 100.00 0 SDHA 100.00 0 SYNE1 100.00 0 CALR3 100.00 0 JPH2 100.00 0 ALPK3 100.00 0 MYL3 100.00 0 MYOZ2 100.00 0 MYPN 100.00 0 PPA2 100.00 0 CALR3 100.00 0 CDH2 100.00 0 DOLK 100.00 0 JPH2 100.00 0 MYL3 100.00 0 MYLK3 100.00 0 MYOZ2 100.00 0 NRAP 100.00 0 RPL3L 100.00 0 TNNI3K 100.00 0 -
Dilated Cardiomyopathy (79 genes) - IPG
Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments ABCC9 100.00 1 NM_020297.3 ACTC1 100.00 1 NM_005159.5 ACTN2 100.00 1 NM_001103.3 ANK2 100.00 1 NM_001148.6 ANKRD1 100.00 1 NM_014391.2 BAG3 100.00 1 NM_004281.4 CASQ2 100.00 1 NM_001232.3 CAV3 100.00 1 NM_033337.3 CDH2 100.00 1 NM_001792.5 CRYAB 100.00 1 NM_001289808.2 CSRP3 100.00 1 NM_003476.5 CTF1 100.00 1 NM_001330.3 DES 100.00 1 NM_001927.4 DMD 100.00 1 NM_004006.2 DOLK 100.00 1 NM_014908.4 DSC2 100.00 1 NM_024422.6 DSG2 100.00 1 NM_001943.5 DSP 100.00 1 NM_004415.4 DTNA 100.00 1 NM_001198938.2 EMD 100.00 1 NM_000117.3 EYA4 100.00 1 NM_004100.5 FHL1 100.00 1 NM_001159699.2 FHL2 100.00 1 NM_201555.2 FHOD3 100.00 1 NM_001281740.3 FKRP 100.00 1 NM_024301.5 FKTN 100.00 1 NM_006731.2 FLII 100.00 1 NM_002018.4 FLNC 100.00 1 NM_001458.4 GATA6 100.00 1 NM_005257.5 GATAD1 100.00 1 NM_021167.5 GLA 100.00 1 NM_000169.3 ILK 100.00 1 NM_004517.4 JPH2 100.00 1 NM_020433.5 JUP 100.00 1 NM_002230.4 LAMA4 100.00 1 NM_001105206.3 LAMP2 100.00 1 NM_002294.3 LDB3 100.00 1 NM_001171610.2 LMNA 100.00 1 NM_170707.4 MIB1 100.00 1 NM_020774.3 MYBPC3 100.00 1 NM_000256.3 MYH6 100.00 1 NM_002471.3 MYH7 100.00 1 NM_000257.4 MYL2 100.00 1 NM_000432.4 MYL3 100.00 1 NM_000258.3 MYLK2 100.00 1 NM_033118.4 MYLK3 100.00 1 NM_182493.3 MYOZ2 100.00 1 NM_016599.5 MYPN 100.00 1 NM_032578.3 NEBL 100.00 1 NM_006393.2 NEXN 100.00 1 NM_144573.3 NKX2-5 100.00 1 NM_004387.4 NRAP 100.00 1 NM_198060.4 OBSCN 100.00 1 NM_001271223.2 PKP2 100.00 1 NM_001005242.3 PLEKHM2 100.00 1 NM_015164.4 PLN 100.00 1 NM_002667.5 PRDM16 100.00 1 NM_022114.4 PRKAG2 100.00 1 NM_016203.4 PSEN2 100.00 1 NM_000447.3 RAF1 100.00 1 NM_001354689.3 RBM20 100.00 1 NM_001134363.3 RPL3L 100.00 1 NM_005061.3 RYR2 100.00 1 NM_001035.3 SCN5A 100.00 1 NM_000335.5 SGCD 100.00 1 XM_017009724.1 SPEG 100.00 1 NM_005876.5 TBX20 100.00 1 NM_001077653.2 TBX5 100.00 1 NM_181486.4 TCAP 100.00 1 NM_003673.4 TMEM43 100.00 1 NM_024334.3 TNNC1 100.00 1 NM_003280.3 TNNI3 100.00 1 NM_000363.5 TNNI3K 100.00 1 NM_015978.3 TNNT2 100.00 1 NM_001276345.2 TPM1 100.00 1 NM_001018005.2 TTN 99.52 1 NM_001267550.2 TTR 100.00 1 NM_000371.4 VCL 100.00 1 NM_014000.3 TAFAZZIN 100.00 1 NM_000116.5 -
Primary Electrical disorders/Brugada syndrome (genepanel) - UZA
Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments ABCB4 100.00 0 ABCC9 100.00 0 ACTN2 100.00 0 AKAP9 100.00 0 ANK2 100.00 0 CACNA1C 100.00 0 CACNA2D1 100.00 0 CACNB2 100.00 0 CALM1 100.00 0 CALM2 100.00 0 CALM3 100.00 0 CASQ2 100.00 0 CAV3 100.00 0 CTNNA3 100.00 0 DES 100.00 0 DPP6 100.00 0 DSC2 100.00 0 DSG2 100.00 0 DSP 100.00 0 GJA1 100.00 0 GJA5 100.00 0 GNB5 100.00 0 GPD1L 100.00 0 HCN4 100.00 0 JUP 100.00 0 KCNA5 100.00 0 KCND3 100.00 0 KCNE1 100.00 0 KCNE2 100.00 0 KCNE3 100.00 0 KCNE5 100.00 0 KCNH2 100.00 0 KCNJ2 100.00 0 KCNJ5 100.00 0 KCNJ8 100.00 0 KCNK17 100.00 0 KCNQ1 100.00 0 LMNA 100.00 0 NKX2-5 100.00 0 NOS1AP 100.00 0 NPPA 100.00 0 PKP2 100.00 0 PLN 100.00 0 PPA2 100.00 0 PRKAG2 100.00 0 RANGRF 100.00 0 RRAD 100.00 0 RYR2 100.00 0 SCN1B 100.00 0 SCN2B 100.00 0 SCN3B 100.00 0 SCN4B 100.00 0 SCN5A 100.00 0 SCN10A 100.00 0 SLMAP 100.00 0 SNTA1 100.00 0 TGFB3 100.00 0 TMEM43 100.00 0 TRDN 100.00 0 TRPM4 100.00 0 CDH2 100.00 0 CLCA2 100.00 0 FLNC 100.00 0 GNB2 100.00 0 MYL3 100.00 0 MYL4 100.00 0 RBM20 100.00 0 RNF207 100.00 0 SLC4A3 100.00 0 TANGO2 100.00 0 TECRL 100.00 0 TNNI3K 100.00 0 TTN 100.00 0