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Symbol
Name
ID
Dnm1l
dynamin 1-like
MGI:1921256
Phenotype annotations related to mortality/aging
Darker colors indicate more annotations
Human Phenotypes
Death in infancy
Disease(s) Associated with DNM1L
encephalopathy due to defective mitochondrial and peroxisomal fission 1

Mouse Phenotypes
postnatal lethality, complete penetrance
embryonic lethality during organogenesis, complete penetrance
embryonic lethality during organogenesis, incomplete penetrance
prenatal lethality, complete penetrance
preweaning lethality, complete penetrance
Availability Mouse Genotype
Dnm1lPy/Dnm1lPy
Dnm1ltm1.2Hise/Dnm1ltm1.2Hise
Dnm1ltm1.2Miha/Dnm1ltm1.2Miha
Dnm1ltm1b(KOMP)Wtsi/Dnm1ltm1b(KOMP)Wtsi
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
03/12/2024
MGI 6.23
The Jackson Laboratory