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Symbol
Name
ID
Dnm1l
dynamin 1-like
MGI:1921256
Phenotype annotations related to behavior/neurological
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Drooling
Decreased fetal movement
Feeding difficulties
Restlessness
Self-biting
Disease(s) Associated with DNM1L
encephalopathy due to defective mitochondrial and peroxisomal fission 1

Mouse Phenotypes
behavior/neurological phenotype
absent gastric milk in neonates
abnormal pilomotor reflex
Availability Mouse Genotype
Dnm1lem1Hise/Dnm1lem1Hise *
Dnm1lPy/Dnm1l+
Dnm1ltm1.1Hise/Dnm1ltm1.1Hise
En1tm2(cre)Wrst/En1+  (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
03/12/2024
MGI 6.23
The Jackson Laboratory