| Gene Symbol | WDR81 |
| Entrez Gene ID | 124997 |
| Full Name | WD repeat domain 81 |
| Synonyms | CAMRQ2,PPP1R166,SORF-2 |
| General protein information |
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| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | This gene encodes a multi-domain transmembrane protein which is predominantly expressed in the brain and is thought to play a role in endolysosomal trafficking. Mutations in this gene are associated with an autosomal recessive form of a syndrome exhibiting cerebellar ataxia, cognitive disability, and disequilibrium (CAMRQ2). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]. |
| Disorder MIM: | |
| Disorder Html: | Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2, 610185 (3) |

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