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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 02-04-2019 |
Symbol | AA |
Location | 11p15.3 |
HGNC id | 11 |
Name | atrophia areata |
Other name(s) |
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Corresponding gene | TEAD1 |
related resource | Retinal Information Network |
Other symbol(s) | SCRA |
Main clinical features |
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Genetic determination | autosomal dominant |
Function/system disorder | eye |
Type | disease |
Gene product |
Name | TEA domain family member 1 |
Remark(s) | . mutation has been shown previously to disrupt the YAP1-TEAD interaction (Jianzhong 2010) |