hnrnpa2b1 Phenotypes

XB-GENEPAGE-490992

Gene Symbol: hnrnpa2b1 Gene Name: heterogeneous nuclear ribonucleoprotein A2/B1

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (43 sources): Abnormal motor neuron morphology, Abnormality of calvarial morphology, Abnormality of long bone morphology, Abnormality of the vertebral column, Amyotrophic lateral sclerosis, Aphasia, Brain atrophy, Calvarial hyperostosis, Cardiomyopathy, Cataract, Congestive heart failure, Cranial nerve compression, Distal muscle weakness, Dyscalculia, EMG: chronic denervation signs, EMG: myopathic abnormalities, EMG: neuropathic changes, Elevated circulating alkaline phosphatase concentration, Elevated circulating creatine kinase concentration, Fasciculations, Fatty replacement of skeletal muscle, Frontotemporal dementia, Generalized amyotrophy, Hepatic steatosis, Hip pain, Hyperlordosis, Increased susceptibility to fractures, Increased variability in muscle fiber diameter, Intellectual disability, Language impairment, Motor axonal neuropathy, Mutism, Osteolysis, Pathologic fracture, Proximal muscle weakness, Rimmed vacuoles, Sensory axonal neuropathy, Short stature, Ubiquitin-positive cerebral inclusion bodies, Upper motor neuron dysfunction, Urinary bladder sphincter dysfunction, Waddling gait, Weakness of muscles of respiration [+]
Mouse (6 sources): abnormal interferon level, decreased circulating interferon-beta level, decreased interferon-beta secretion, immune system phenotype, increased susceptibility to Herpesvirales infection, increased susceptibility to Herpesvirales infection induced morbidity/mortality
View all ortholog results at Monarch