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Symbol
Name
ID
Uchl1
ubiquitin carboxy-terminal hydrolase L1
MGI:103149
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Hyposmia
Ankle clonus
Dysphagia
Abnormality of visual evoked potentials
Spasticity
Lower limb spasticity
Spastic paraplegia
Peripheral axonal neuropathy
Cerebral atrophy
Cerebellar atrophy
Neurodegeneration
Ataxia
Dysmetria
Gait ataxia
Bradykinesia
Fasciculations
Tremor
Intention tremor
Postural tremor
Head titubation
Babinski sign
Hoffmann sign
Tetraparesis
Dysarthria
Depression
Anxiety
Panic attack
Hallucinations
Apathy
Reduced social reciprocity
Impulsivity
Agitation
Restless legs
Cognitive impairment
Dementia
Frontal lobe dementia
Short attention span
Intellectual disability
Insomnia
Hyperreflexia
Lower limb hyperreflexia
Dyskinesia
Dystonia
Gait imbalance
Loss of ambulation
Myokymia
Postural instability
Sensorimotor neuropathy
Impaired proprioception
Impaired vibratory sensation
Impaired vibration sensation at ankles
Sensory ataxia
Abnormal autonomic nervous system physiology
Disease(s) Associated with UCHL1
hereditary spastic paraplegia 79A
hereditary spastic paraplegia 79B
Parkinson's disease

Mouse Phenotypes
abnormal medulla oblongata morphology
motor neuron degeneration
abnormal neuromuscular synapse morphology
abnormal dorsal root ganglion morphology
abnormal spinal cord dorsal column morphology
neurodegeneration
axon degeneration
axonal dystrophy
abnormal synaptic plasticity
increased synaptic depression
abnormal PNS synaptic transmission
abnormal endplate potential
abnormal miniature endplate potential
decreased neurotransmitter release
decreased paired-pulse facilitation
Availability Mouse Genotype
Uchl1gad-2J/Uchl1gad-2J
Uchl1gad/Uchl1gad
Uchl1tm1Dgen/Uchl1tm1Dgen

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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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory