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Symbol
Name
ID
Dnm1l
dynamin 1-like
MGI:1921256
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Microcephaly
Drooling
Increased CSF lactate
Abnormality of pattern visual evoked potentials
Oculomotor apraxia
Delayed CNS myelination
Cerebral atrophy
Athetosis
Abnormal pyramidal sign
Restlessness
Self-biting
Areflexia
Encephalopathy
Epileptic encephalopathy
Global developmental delay
Motor delay
Seizure
Status epilepticus
Pain insensitivity
Disease(s) Associated with DNM1L
encephalopathy due to defective mitochondrial and peroxisomal fission 1
optic atrophy 5

Mouse Phenotypes
abnormal Purkinje cell mitochondrial morphology
increased neuron apoptosis
increased brain apoptosis
decreased embryonic neuroepithelium thickness
abnormal brain morphology
abnormal cerebellum development
reduced cerebellar foliation
forebrain hypoplasia
enlarged brain ventricles
abnormal brain white matter morphology
abnormal brainstem morphology
abnormal cerebellar Purkinje cell layer
decreased Purkinje cell number
small cerebellum
abnormal subarachnoid space morphology
decreased CNS synapse formation
abnormal neurite morphology
abnormal dendritic spine morphology
abnormal synapse morphology
abnormal optic disk morphology
enhanced sensorimotor gating
increased prepulse inhibition
Availability Mouse Genotype
Dnm1lem1Hise/Dnm1lem1Hise
Dnm1lem1Hise/Dnm1lem1Hise
Tg(Thy1-EGFP)MJrs/0
Dnm1ltm1.2Miha/Dnm1ltm1.2Miha
Dnm1ltm1b(KOMP)Wtsi/Dnm1l+
Dnm1ltm1.1Hise/Dnm1ltm1.1Hise
En1tm2(cre)Wrst/En1+  (conditional)
Dnm1ltm1.1Miha/Dnm1ltm1.1Miha
Tg(Nes-cre)1Kln/0  (conditional)
Dnm1ltm1.1Hise/Dnm1ltm1.2Hise
En1tm2(cre)Wrst/En1+  (conditional)

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