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Symbol
Name
ID
Dnm1l
dynamin 1-like
MGI:1921256
Phenotype annotations related to embryo
Darker colors indicate more annotations
Human Phenotypes
Decreased fetal movement
Disease(s) Associated with DNM1L
encephalopathy due to defective mitochondrial and peroxisomal fission 1

Mouse Phenotypes
caudal body truncation
embryonic growth retardation
decreased embryo size
decreased embryonic neuroepithelium thickness
absent trophoblast giant cells
Availability Mouse Genotype
Dnm1lPy/Dnm1lPy
Dnm1ltm1.2Hise/Dnm1ltm1.2Hise
Dnm1ltm1.2Miha/Dnm1ltm1.2Miha

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