slc33a1 Phenotypes

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Phenotypes

Gene Literature (0)

Nucleotides (180)

Interactants (57)

XB-GENEPAGE-971527

Gene Symbol: slc33a1 Gene Name: solute carrier family 33 (acetyl-CoA transporter), member 1

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (32 sources): Absent speech, Babinski sign, CNS hypomyelination, Cataract, Cerebellar atrophy, Cerebral atrophy, Clonus, Decreased circulating ceruloplasmin concentration, Degeneration of the lateral corticospinal tracts, Developmental cataract, Generalized hypotonia, Global developmental delay, Hearing impairment, Hyperreflexia, Hypotonia, Impaired vibration sensation in the lower limbs, Lower limb amyotrophy, Lower limb hyperreflexia, Lower limb hypertonia, Lower limb muscle weakness, Lower limb spasticity, Muscle weakness, Nystagmus, Pes cavus, Progressive pes cavus, Progressive spastic paraplegia, Psychomotor retardation, Seizure, Skeletal muscle atrophy, Spastic gait, Spastic paraplegia, Spinal cord lesion [+]
Mouse (27 sources): abnormal T cell activation, abnormal autophagy, abnormal circulating cytokine level, abnormal motor capabilities/coordination/movement, abnormal spinal cord white matter morphology, decreased corpus callosum size, decreased grip strength, decreased survivor rate, dermatitis, embryonic growth arrest, embryonic growth retardation, immune system phenotype, increased circulating interleukin-17 level, increased circulating interleukin-18 level, increased interferon-gamma secretion, increased interleukin-17 secretion, increased interleukin-4 secretion, increased lung adenoma incidence, increased lymphoma incidence, increased neutrophil cell number, increased thermal nociceptive threshold, increased tumor incidence, limb grasping, microgliosis, neuron degeneration, preputial gland inflammation, salivary gland inflammation [+]
View all ortholog results at Monarch