| Human Disease |
Albinism, Oculocutaneous, Type IA; OCA1A OMIM ID: 203100 |
|||||||||||||||||||||
| Synonyms | Albinism I; Oculocutaneous Albinism, Type I; OCA1; Oculocutaneous Albinism, Tyrosinase-Negative; ATN | |||||||||||||||||||||
| View all models | View ALL (1) mouse models for this human disease. | |||||||||||||||||||||
|
Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
|
|||||||||||||||||||||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
||
|
Citing These Resources Funding Information Warranty Disclaimer & Copyright Notice Send questions and comments to User Support. |
last database update 05/08/2013 MGI 5.13 |
|
|
|
||