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| Dilated Cardiomyopathy v1.42 | NEXN | Zornitza Stark Mode of inheritance for gene: NEXN was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dilated Cardiomyopathy v1.41 | NEXN | Zornitza Stark edited their review of gene: NEXN: Changed publications: 19881492, 28416588, 25163546, 27532257, 24503780, 29540472; Changed phenotypes: Cardiomyopathy, dilated, 1CC, MIM# 613122; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dilated Cardiomyopathy v1.41 | NEXN | Zornitza Stark Phenotypes for gene: NEXN were changed from Cardiomyopathy, dilated, 1CC, MIM# 613122; Cardiomyopathy, dilated, 2M, autosomal recessive, MIM# 621261 to Cardiomyopathy, dilated, 1CC, MIM# 613122 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dilated Cardiomyopathy v1.40 | NEXN | Zornitza Stark Deleted their comment | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dilated Cardiomyopathy v1.40 | NEXN | Zornitza Stark Phenotypes for gene: NEXN were changed from Cardiomyopathy, dilated, 1CC, MIM# 613122 to Cardiomyopathy, dilated, 1CC, MIM# 613122; Cardiomyopathy, dilated, 2M, autosomal recessive, MIM# 621261 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dilated Cardiomyopathy v1.39 | NEXN | Zornitza Stark Mode of inheritance for gene: NEXN was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to BOTH monoallelic and biallelic, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dilated Cardiomyopathy v1.38 | NEXN | Zornitza Stark edited their review of gene: NEXN: Added comment: 7 families reported with DCM and bi-allelic variants, several of the presentations were severe perinatal.; Changed publications: 19881492, 28416588, 25163546, 27532257, 24503780, 29540472, 26659360, 33949776, 39183344, 38059363, 35166435; Changed phenotypes: Cardiomyopathy, dilated, 1CC, MIM# 613122, Cardiomyopathy, dilated, 2M, autosomal recessive, MIM# 621261; Changed mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dilated Cardiomyopathy v0.142 | NEXN | Zornitza Stark Tag for review tag was added to gene: NEXN. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dilated Cardiomyopathy v0.139 | NEXN | Zornitza Stark Marked gene: NEXN as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dilated Cardiomyopathy v0.139 | NEXN | Zornitza Stark Gene: nexn has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dilated Cardiomyopathy v0.139 | NEXN | Zornitza Stark Phenotypes for gene: NEXN were changed from to Cardiomyopathy, dilated, 1CC, MIM# 613122 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dilated Cardiomyopathy v0.138 | NEXN | Zornitza Stark Publications for gene: NEXN were set to | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dilated Cardiomyopathy v0.137 | NEXN | Zornitza Stark Mode of inheritance for gene: NEXN was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dilated Cardiomyopathy v0.136 | NEXN | Zornitza Stark reviewed gene: NEXN: Rating: GREEN; Mode of pathogenicity: None; Publications: 19881492, 28416588, 25163546, 27532257, 24503780, 29540472, 26659360; Phenotypes: Cardiomyopathy, dilated, 1CC, MIM# 613122; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Dilated Cardiomyopathy v0.0 | NEXN |
Zornitza Stark gene: NEXN was added gene: NEXN was added to Dilated cardiomyopathy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: NEXN was set to Unknown |
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