|
Symbol Name ID |
Fbn2
fibrillin 2 MGI:95490 |
| Darker colors indicate more annotations |
| Human Phenotypes | Camptodactyly of finger |
Congenital finger flexion contractures |
Hip contracture |
Knee flexion contracture |
Calf muscle hypoplasia |
Elbow flexion contracture |
Wrist flexion contracture |
Flexion contracture |
Congenital contracture |
Arthrogryposis multiplex congenita |
Distal arthrogryposis |
Camptodactyly |
Abnormality of the musculature |
| Disease(s) Associated with FBN2 | |||||||||||||
| congenital contractural arachnodactyly |
| Mouse Phenotypes | decreased skeletal muscle fiber diameter |
centrally nucleated skeletal muscle fibers |
increased skeletal muscle mass |
abnormal muscle electrophysiology |
muscle weakness |
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| Availability | Mouse Genotype | |||||
| Fbn2fp/Fbn2fp | ||||||
| Fbn2mz/Fbn2mz | ||||||
| Fbn2fp/Fbn2mz | ||||||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/16/2024 MGI 6.23 |
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