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Symbol
Name
ID

Kbtbd13
kelch repeat and BTB (POZ) domain containing 13
MGI:1921742

Phenotype annotations related to muscle

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Facial palsy	Limb muscle weakness	Difficulty climbing stairs	Difficulty running	Muscle stiffness	Neck flexor weakness	Nemaline bodies	Skeletal muscle atrophy	Myopathy
Disease(s) Associated with KBTBD13
nemaline myopathy 6

Mouse Phenotypes		muscle phenotype	increased quadriceps weight	abnormal soleus morphology	decreased soleus weight	increased soleus weight	abnormal skeletal muscle fiber morphology	thick diaphragm muscle	impaired muscle relaxation
Availability	Mouse Genotype	muscle phenotype	increased quadriceps weight	abnormal soleus morphology	decreased soleus weight	increased soleus weight	abnormal skeletal muscle fiber morphology	thick diaphragm muscle	impaired muscle relaxation
	Kbtbd13^em1Coeo/Kbtbd13^em1Coeo
	Kbtbd13^tm1.1Coeo/Kbtbd13^tm1.1Coeo	*

Contributing Projects: 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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