| Gene Symbol | PCDH19 |
| Entrez Gene ID | 57526 |
| Full Name | protocadherin 19 |
| Synonyms | EFMR,EIEE9 |
| General protein information |
|
| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | The protein encoded by this gene is a member of the delta-2 protocadherin subclass of the cadherin superfamily. The encoded protein is thought to be a calcium-dependent cell-adhesion protein that is primarily expressed in the brain. Mutations in this gene on human chromosome X are associated with sporadic infantile epileptic encephalopathy and to a female-restricted form of epilepsy (EFMR; also known as PCDH19RE). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]. |
| Disorder MIM: | |
| Disorder Html: | Epileptic encephalopathy, early infantile, 9, 300088 (3) |







































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