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Symbol
Name
ID
Atl1
atlastin GTPase 1
MGI:1921241
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Ankle clonus
Lower limb spasticity
Spastic paraplegia
Spastic gait
Frequent falls
Peripheral axonal neuropathy
Hypoplasia of the corpus callosum
Degeneration of the lateral corticospinal tracts
Bradykinesia
Babinski sign
Paraplegia
Dysarthria
Intellectual disability, mild
Hyperreflexia
Lower limb hyperreflexia
Gait disturbance
Tip-toe gait
Motor delay
Peripheral neuropathy
Distal sensory impairment of all modalities
Hyperesthesia
Paresthesia
Distal sensory impairment
Impaired vibratory sensation
Impaired vibration sensation in the lower limbs
Disease(s) Associated with ATL1
hereditary sensory neuropathy type 1D
hereditary spastic paraplegia 3A

Mouse Phenotypes
abnormal corticospinal tract morphology
abnormal myelin sheath morphology
Availability Mouse Genotype
Atl1tm1.1Cbla/Atl1tm1.1Cbla
Atl1tm1.2Cbla/Atl1tm1.2Cbla

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
04/30/2024
MGI 6.23
The Jackson Laboratory