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DDG2P v3.12 | MN1 | Achchuthan Shanmugasundram reviewed gene: MN1: Rating: GREEN; Mode of pathogenicity: ; Publications: 31839203, 31834374; Phenotypes: MN1 C-terminal truncation syndrome , OMIM:618774; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
DDG2P v3.11 | MN1 |
Achchuthan Shanmugasundram Source Expert Review Green was added to MN1. Publications for gene: MN1 were updated from 21242494 to 31839203; 31834374; 21242494 Rating Changed from Amber List (moderate evidence) to Green List (high evidence) |
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DDG2P v1.74 | MN1 | Rebecca Foulger commented on gene: MN1 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
DDG2P v1.73 | MN1 |
Rebecca Foulger gene: MN1 was added gene: MN1 was added to DDG2P. Sources: DD-Gene2Phenotype,Expert Review Amber Mode of inheritance for gene: MN1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: MN1 were set to 21242494 Phenotypes for gene: MN1 were set to MN1 C-terminal truncation syndrome |