This panel contains genes that cause isolated congenital mirror movements. It does not contain genes associated with mirror movements as a component of a syndromic phenotype.
Bryony Thompson (Royal Melbourne Hospital)
List | Entity | Reviews | Mode of inheritance | Details | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Green List (high evidence) |
DCC |
1 review1 green |
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted |
Sources
Phenotypes
Tags |
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Green List (high evidence) |
NTN1 |
1 review1 green |
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted |
Sources
Phenotypes
Tags |
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Green List (high evidence) |
RAD51 |
1 review1 green |
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted |
Sources
Phenotypes
Tags |
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Red List (low evidence) |
DNAL4 |
1 review1 red |
BIALLELIC, autosomal or pseudoautosomal |
Sources
Phenotypes
Tags |
2021-09-02 02:08 Bryony Thompson (Royal Melbourne Hospital) promoted panel to 1.0
All genes on panel reviewed, ready for promotion.