sgcd Phenotypes

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Phenotypes

Gene Literature (1)

Nucleotides (79)

Interactants (7)

XB-GENEPAGE-949517

Gene Symbol: sgcd Gene Name: sarcoglycan delta

Expression Phenotypes Gene expression phenotype annotations where the gene of interest has been disrupted (manipulated) or is the gene assayed (assayed). Computed annotations are derived from differential expression analysis from Xenbase processed GEO data with the criteria of a TPM >= 1, FDR <= 0.05 and an absolute LogFC >= 2.
Computed annotations: sgcd assayed (2 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (25 sources): Abnormality of neutrophils, Calf muscle hypertrophy, Cleft palate, Congestive heart failure, Difficulty walking, Dilated cardiomyopathy, EMG abnormality, Elevated circulating creatine kinase concentration, Facial palsy, Generalized limb muscle atrophy, Gowers sign, Lipoatrophy, Muscular dystrophy, Myopathy, Palmoplantar keratoderma, Proximal amyotrophy, Proximal lower limb amyotrophy, Proximal muscle weakness, Proximal upper limb amyotrophy, Reduced systolic function, Scapular winging, Sensorineural hearing impairment, Shuffling gait, Strabismus, Ventricular hypertrophy [+]
Mouse (16 sources): abnormal muscle contractility, abnormal response to exercise, cardiac fibrosis, cardiac muscle degeneration, cardiac muscle necrosis, decreased QRS amplitude, decreased aerobic running capacity, decreased cardiac muscle contractility, dystrophic cardiac calcinosis, increased heart weight, increased sensitivity to induced morbidity/mortality, muscle degeneration, perivascular fibrosis, premature death, prenatal lethality, complete penetrance, skeletal muscle necrosis [+]
View all ortholog results at Monarch