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Symbol
Name
ID
Flnc
filamin C, gamma
MGI:95557
Phenotype annotations related to muscle
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Weakness of facial musculature
Abnormal calf musculature morphology
Distal lower limb muscle weakness
Intrinsic hand muscle atrophy
Finger flexor weakness
Thenar muscle weakness
Distal upper limb amyotrophy
Foot dorsiflexor weakness
Proximal muscle weakness in lower limbs
Hip flexor weakness
Distal upper limb muscle weakness
Difficulty climbing stairs
Difficulty running
Difficulty walking
Muscle weakness
Fatiguable weakness of proximal limb muscles
Proximal muscle weakness
Respiratory insufficiency due to muscle weakness
Muscle fiber cytoplasmatic inclusion bodies
Muscle fiber splitting
Skeletal muscle atrophy
Distal lower limb amyotrophy
Myopathy
Myofibrillar myopathy
Disease(s) Associated with FLNC
distal myopathy 4
myofibrillar myopathy 5

Mouse Phenotypes
muscle phenotype
abnormal extensor digitorum longus morphology
abnormal soleus morphology
abnormal tibialis anterior morphology
abnormal myogenesis
abnormal muscle fiber morphology
abnormal sarcomere morphology
abnormal Z line morphology
abnormal skeletal muscle fiber morphology
increased variability of skeletal muscle fiber size
centrally nucleated skeletal muscle fibers
decreased skeletal muscle fiber number
skeletal muscle fiber degeneration
abnormal skeletal muscle morphology
abnormal diaphragm morphology
abnormal intercostal muscle morphology
decreased skeletal muscle mass
Availability Mouse Genotype
Flnctm1Lmk/Flnctm1Lmk
Flnctm1.1Rsdf/Flnc+ *

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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory