Symbol Name ID |
Klhl40
kelch-like 40 MGI:1919580 |
Darker colors indicate more annotations |
Human Phenotypes | Facial palsy |
Flexion contracture |
Muscle weakness |
Nemaline bodies |
Myofibrillar myopathy |
Disease(s) Associated with KLHL40 | |||||
nemaline myopathy 8 |
Mouse Phenotypes | increased skeletal muscle cell apoptosis |
abnormal sarcomere morphology |
abnormal Z line morphology |
decreased skeletal muscle fiber size |
abnormal skeletal muscle morphology |
abnormal muscle physiology |
impaired skeletal muscle contractility |
muscle weakness |
myopathy |
|
Availability | Mouse Genotype | |||||||||
Klhl40tm1(KOMP)Vlcg/Klhl40tm1(KOMP)Vlcg | ||||||||||
Klhl40tm1.1Itl/Klhl40tm1.1Itl |
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 08/02/2024 MGI 6.24 |
|
|