Symbol Name ID |
Dnm1l
dynamin 1-like MGI:1921256 |
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 |
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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) |
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Dnm1ltm1.1Miha/Dnm1ltm1.1Miha Tg(Nes-cre)1Kln/0 (conditional) |
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Dnm1ltm1.1Hise/Dnm1ltm1.2Hise En1tm2(cre)Wrst/En1+ (conditional) |
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 |
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