|
Symbol Name ID |
Aldh3a2
aldehyde dehydrogenase family 3, subfamily A2 MGI:1353452 |
| Darker colors indicate more annotations |
| Human Phenotypes | Erythema |
Urticaria |
Abnormal hair morphology |
Abnormality of the nail |
Generalized hyperpigmentation |
Dry skin |
Hyperkeratosis |
Ichthyosis |
| Disease(s) Associated with ALDH3A2 | ||||||||
| Sjogren-Larsson syndrome |
| Mouse Phenotypes | increased keratinocyte proliferation |
abnormal epidermis stratum basale morphology |
abnormal epidermis stratum granulosum morphology |
abnormal epidermis stratum spinosum morphology |
delayed skin barrier formation |
abnormal keratinocyte physiology |
|
| Availability | Mouse Genotype | ||||||
| Aldh3a2tm1b(EUCOMM)Wtsi/Aldh3a2tm1b(EUCOMM)Wtsi | |||||||
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 04/23/2024 MGI 6.23 |
|
|
|
||
Analysis Tools