| Standard Name | CVT6 |
|---|---|
| Feature Type | not physically mapped |
Mutant phenotypes All CVT6 Phenotype evidence and references
| Classical genetics | |
|---|---|
| reduction of function |
|
Resources
| External Links | Search all NCBI (Entrez) |
|---|
| Primary SGDID | S000029131 |
|---|
| Standard Name | CVT6 |
|---|---|
| Feature Type | not physically mapped |
| Classical genetics | |
|---|---|
| reduction of function |
|
| External Links | Search all NCBI (Entrez) |
|---|
| Primary SGDID | S000029131 |
|---|