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| Genomic screening in children: BabyScreen+ v0.91 | NEUROD1 |
Zornitza Stark Tag treatable tag was added to gene: NEUROD1. Tag endocrine tag was added to gene: NEUROD1. |
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| Genomic screening in children: BabyScreen+ v0.75 | NEUROD1 | Zornitza Stark Marked gene: NEUROD1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic screening in children: BabyScreen+ v0.75 | NEUROD1 | Zornitza Stark Gene: neurod1 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic screening in children: BabyScreen+ v0.75 | NEUROD1 | Zornitza Stark Phenotypes for gene: NEUROD1 were changed from Maturity Onset Diabetes of the Young; {Diabetes mellitus, noninsulin-dependent}, 125853 to Maturity-onset diabetes of the young 6, MIM#606394 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic screening in children: BabyScreen+ v0.74 | NEUROD1 | Zornitza Stark Mode of inheritance for gene: NEUROD1 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic screening in children: BabyScreen+ v0.73 | NEUROD1 |
Zornitza Stark changed review comment from: Mono-allelic variants in this gene are associated with MODY. Rare reports of bi-allelic variants, sometimes with permanent neonatal diabetes, RP/retinopathy reported in three unrelated individuals. Functional data to support gene's role in retina.; to: Mono-allelic variants in this gene are associated with MODY. |
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| Genomic screening in children: BabyScreen+ v0.73 | NEUROD1 | Zornitza Stark edited their review of gene: NEUROD1: Changed phenotypes: Maturity-onset diabetes of the young 6, MIM#606394; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic screening in children: BabyScreen+ v0.71 | Zornitza Stark Copied gene NEUROD1 from panel Maturity-onset Diabetes of the Young | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic screening in children: BabyScreen+ v0.71 | NEUROD1 |
Zornitza Stark gene: NEUROD1 was added gene: NEUROD1 was added to Genomic screening in children: BabyScreen+. Sources: Expert Review Green,Royal Melbourne Hospital,Victorian Clinical Genetics Services Mode of inheritance for gene: NEUROD1 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal Publications for gene: NEUROD1 were set to 25477324; 25684977; 22784109; 29521454 Phenotypes for gene: NEUROD1 were set to Maturity Onset Diabetes of the Young; {Diabetes mellitus, noninsulin-dependent}, 125853 |
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