- Analytes
- TNNC1
TNNC1
Name: |
troponin C1, slow skeletal and cardiac type
|
Symbol: |
TNNC1
|
Version of Orphanet: |
2023-06-22 14:14:43
|
XREF(s): | |
Created: |
13 May 2019 - 01:01
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Changed: |
22 Jun 2023 - 16:14
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- Cardiomyopathy, hypertrophic
- Cardiomyopathy: hypertrophic cardiomyopathy, dilated cardiomyopathy, restrictive cardiomyopathy, left ventricular non-compaction cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy (gene panel)
- Dilated Cardiomyopathy (Gene panel)
- Dilated cardiomyopathy
- Hypertrophic cardiomyopathy (gene panel)
-
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 -
Dilated cardiomyopathy - UGent
Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments LMNA 100.00 1 TTN 100.00 1 ACTC1 100.00 1 BAG3 100.00 1 DES 100.00 1 DSP 100.00 1 FLNC 100.00 1 JPH2 100.00 1 MYH7 100.00 1 NEXN 100.00 1 RBM20 100.00 1 SCN5A 100.00 1 TNNI3 100.00 1 TNNC1 100.00 1 TNNT2 100.00 1 TPM1 100.00 1 VCL 100.00 1 -
Hypertrophic cardiomyopathy (75 genes) - IPG
Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments ACTC1 100.00 1 NM_005159.5 ACTN2 100.00 1 NM_001103.3 ALPK3 100.00 1 NM_020778.5 CSRP3 100.00 1 NM_003476.5 GLA 100.00 1 NM_000169.3 JPH2 100.00 1 NM_020433.5 LAMP2 100.00 1 NM_002294.3 LMNA 100.00 1 NM_170707.4 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 PLN 100.00 1 NM_002667.5 PRKAG2 100.00 1 NM_016203.4 TNNC1 100.00 1 NM_003280.3 TNNI3 100.00 1 NM_000363.5 TNNT2 100.00 1 NM_001276345.2 TPM1 100.00 1 NM_001018005.2 TTR 100.00 1 NM_000371.4 ACADVL 100.00 1 NM_000018.4 ACTA1 100.00 1 NM_001100.4 AGL 100.00 1 NM_000642.3 ANKRD1 100.00 1 NM_014391.2 ATAD3A 100.00 1 NM_001170535.3 ATP5F1E 100.00 1 NM_006886.4 BRAF 100.00 1 NM_001354609.2 CACNA1C 100.00 1 NM_000719.7 CALR3 100.00 1 NM_145046.5 CASQ2 100.00 1 NM_001232.3 CAV3 100.00 1 NM_033337.3 COA5 100.00 1 NM_001008215.3 CRYAB 100.00 1 NM_001289808.2 DES 100.00 1 NM_001927.4 FHL1 100.00 1 NM_001159699.2 FHOD3 100.00 1 NM_001281740.3 FLNC 100.00 1 NM_001458.4 FOXRED1 100.00 1 NM_017547.4 FXN 100.00 1 NM_000144.5 GAA 100.00 1 NM_000152.5 GLB1 100.00 1 NM_000404.4 GUSB 100.00 1 NM_000181.4 GYG1 100.00 1 NM_004130.4 HRAS 100.00 1 NM_005343.4 KCNQ1 100.00 1 NM_000218.3 KLF10 100.00 1 NM_005655.4 LDB3 100.00 1 NM_001171610.2 LZTR1 100.00 1 NM_006767.4 MAP2K1 100.00 1 NM_002755.4 MAP2K2 100.00 1 NM_030662.4 MIB1 100.00 1 NM_020774.3 MRPL3 100.00 1 NM_007208.4 MT-TI 100.00 1 MT-TL1 100.00 1 MYLK2 100.00 1 NM_033118.4 MYO6 100.00 1 NM_004999.4 MYOM1 100.00 1 NM_003803.4 MYOZ2 100.00 1 NM_016599.5 MYPN 100.00 1 NM_032578.3 NEXN 100.00 1 NM_144573.3 NRAS 100.00 1 NM_002524.5 PDLIM3 100.00 1 NM_014476.6 PTPN11 100.00 1 NM_002834.5 RAF1 100.00 1 NM_001354689.3 RYR2 100.00 1 NM_001035.3 SCO2 100.00 1 NM_005138.3 SLC25A3 100.00 1 NM_002635.4 SLC25A4 100.00 1 NM_001151.4 SOS1 100.00 1 NM_005633.3 TCAP 100.00 1 NM_003673.4 TMEM70 100.00 1 NM_017866.6 TRIM63 100.00 1 NM_032588.3 TSFM 100.00 1 NM_005726.6 TTN 100.00 1 NM_001267550.2 VCL 100.00 1 NM_014000.3 -
Hypertrophic cardiomyopathy - UGent
Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments MYBPC3 100.00 1 MYH7 100.00 1 TNNT2 100.00 1 ACTC1 100.00 1 PRKAG2 100.00 1 CSRP3 100.00 1 JPH2 100.00 1 MYL2 100.00 1 MYL3 100.00 1 TNNC1 100.00 1 TNNI3 100.00 1 TPM1 100.00 1