trim32 Phenotypes

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Phenotypes

Gene Literature (0)

Nucleotides (85)

Interactants (55)

XB-GENEPAGE-1011958

Gene Symbol: trim32 Gene Name: tripartite motif containing 32

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (49 sources): Abnormal electroretinogram, Areflexia, Calf muscle pseudohypertrophy, Centrally nucleated skeletal muscle fibers, Cryptorchidism, Downslanted palpebral fissures, EMG abnormality, EMG: myopathic abnormalities, Elevated circulating creatine kinase concentration, Exercise-induced myalgia, Facial palsy, Finger syndactyly, Gait disturbance, Generalized hirsutism, Gowers sign, Hearing impairment, Hepatic fibrosis, Hypertension, Hypogonadism, Hypoplasia of penis, Hypoplasia of the ovary, Hyporeflexia, Increased variability in muscle fiber diameter, Intellectual disability, Low-set, posteriorly rotated ears, Mask-like facies, Medial flaring of the eyebrow, Multicystic kidney dysplasia, Muscular dystrophy, Myopathy, Neck flexor weakness, Nephrotic syndrome, Neurological speech impairment, Nystagmus, Obesity, Pelvic girdle muscle atrophy, Pelvic girdle muscle weakness, Pigmentary retinopathy, Postaxial hand polydactyly, Prominent nasal bridge, Proximal muscle weakness in lower limbs, Quadriceps muscle weakness, Short neck, Short stature, Shoulder girdle muscle atrophy, Shoulder girdle muscle weakness, Skeletal muscle atrophy, Tall stature, Waddling gait [+]
Mouse (14 sources): abnormal axon morphology, abnormal physiological response to xenobiotic, abnormal skeletal muscle fiber type ratio, abnormal skeletal muscle morphology, decreased grip strength, decreased litter size, decreased muscle weight, decreased skeletal muscle fiber diameter, impaired skeletal muscle regeneration, increased satellite cell number, increased variability of skeletal muscle fiber size, muscle phenotype, reduced fertility, weakness [+]
View all ortholog results at Monarch