|
Symbol Name ID |
Ufsp2
UFM1-specific peptidase 2 MGI:1913679 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Abnormality of the epiphysis of the femoral head |
Avascular necrosis of the capital femoral epiphysis |
Flat capital femoral epiphysis |
Irregular capital femoral epiphysis |
Wide proximal femoral metaphysis |
Broad femoral neck |
Coxa vara |
Abnormal ossification involving the femoral head and neck |
Shallow acetabular fossae |
Abnormal epiphysis morphology |
Hip dysplasia |
Kyphosis |
Scoliosis |
Abnormal bone ossification |
Abnormality of bone mineral density |
Osteoarthritis |
| Disease(s) Associated with UFSP2 | |||||||||||||||||
| Beukes hip dysplasia | |||||||||||||||||
| developmental and epileptic encephalopathy 106 |
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 04/30/2024 MGI 6.23 |
|
|
|
||
Analysis Tools