Symbol Name ID |
Oca2
oculocutaneous albinism II MGI:97454 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Mouse Phenotypes | behavior/neurological phenotype |
abnormal motor capabilities/coordination/movement |
abnormal motor coordination/balance |
jerky movement |
nervous |
abnormal maternal nurturing |
|
Availability | Mouse Genotype | ||||||
Oca2p-103G/Oca2p-103G | |||||||
Oca2p-bs/Oca2p-bs | |||||||
Oca2p-dn/Oca2p-dn | * | ||||||
Oca2p-s/Oca2p-s |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 05/21/2024 MGI 6.23 |
|
|