Symbol
Name
ID

Sgcd
sarcoglycan, delta (dystrophin-associated glycoprotein)
MGI:1346525

Phenotype annotations related to muscle

Darker colors indicate more annotations

Human Phenotypes

Facial palsy

Calf muscle hypertrophy

Proximal lower limb amyotrophy

Proximal upper limb amyotrophy

Scapular winging

Limb-girdle muscular dystrophy

Difficulty climbing stairs

Difficulty walking

Muscle weakness

Proximal muscle weakness

Gowers sign

Myotonia

Central core regions in muscle fibers

Generalized limb muscle atrophy

Proximal amyotrophy

Muscular dystrophy

Myopathy

Disease(s) Associated with SGCD

autosomal recessive limb-girdle muscular dystrophy type 2F

muscular dystrophy

Mouse Phenotypes

myocardium necrosis

cardiac muscle degeneration

cardiac muscle necrosis

dilated cardiomyopathy

decreased cardiac muscle contractility

cardiomyopathy

skeletal muscle necrosis

abnormal skeletal muscle morphology

skeletal muscle fibrosis

dystrophic muscle

muscle degeneration

abnormal muscle physiology

abnormal muscle contractility

Availability

Mouse Genotype

Sgcd^tm1Kcam/Sgcd^tm1Kcam

Sgcd^tm1Mcn/Sgcd^tm1Mcn

Sgcd^tm1Ojml/Sgcd⁺

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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