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Symbol
Name
ID
Sgca
sarcoglycan, alpha (dystrophin-associated glycoprotein)
MGI:894698
Phenotype annotations related to muscle
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Achilles tendon contracture
Calf muscle pseudohypertrophy
Scapular winging
Difficulty climbing stairs
Frequent falls
Proximal muscle weakness
Gowers sign
Muscular dystrophy
Disease(s) Associated with SGCA
autosomal recessive limb-girdle muscular dystrophy type 2D

Mouse Phenotypes
muscle phenotype
cardiac muscle necrosis
cardiomyopathy
increased extensor digitorum longus weight
increased soleus weight
abnormal muscle fiber morphology
abnormal sarcolemma morphology
abnormal skeletal muscle fiber morphology
centrally nucleated skeletal muscle fibers
increased muscle weight
abnormal skeletal muscle morphology
skeletal muscle fibrosis
calcified muscle
dystrophic muscle
abnormal muscle physiology
abnormal muscle contractility
impaired skeletal muscle contractility
Availability Mouse Genotype
Sgcatm1Eeng/Sgcatm1Eeng
Sgcatm1Isrd/Sgcatm1Isrd *
Sgcatm1Kcam/Sgcatm1Kcam *
Sgcatm2Kcam/Sgcatm2Kcam
Sgcatm2Kcam/Sgcatm2Kcam
Tg(Ckmm-cre)5Khn/0  (conditional)
*

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
07/02/2024
MGI 6.13
The Jackson Laboratory