| Gene Symbol | FAM126A |
| Entrez Gene ID | 84668 |
| Full Name | family with sequence similarity 126 member A |
| Synonyms | DRCTNNB1A,HCC,HLD5,HYCC1 |
| General protein information |
|
| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | The protein encoded by this gene may play a part in the beta-catenin/Lef signaling pathway. Expression of this gene is down-regulated by beta-catenin. Defects in this gene are a cause of hypomyelination with congenital cataract (HCC). [provided by RefSeq, Oct 2008]. |
| Disorder MIM: | |
| Disorder Html: | Leukodystrophy, hypomyelinating, 5, 610532 (3) |
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