MN1 proto-oncogene, transcriptional regulator
OMIM: 156100, Gene2Phenotype
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MN1 in Malformations of cortical development
Level 3: Neurodevelopmental disorders
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review | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown |
Sources
Phenotypes
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MN1 in Fetal anomalies
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review | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown |
Sources
Phenotypes
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MN1 in DDG2P
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review | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown |
Sources
Phenotypes
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MN1 in Monogenic hearing loss
Level 3: Non-syndromic hearing loss
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review | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown |
Sources
Phenotypes
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MN1 in Intellectual disability - microarray and sequencing
Level 3: Neurodevelopmental disorders
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review | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown |
Sources
Phenotypes
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