Symbol Name ID |
Dnm1l
dynamin 1-like MGI:1921256 |
* | 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 |
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Availability | Mouse Genotype | |||
Dnm1lem1Hise/Dnm1lem1Hise | * | |||
Dnm1lPy/Dnm1l+ | ||||
Dnm1ltm1.1Hise/Dnm1ltm1.1Hise En1tm2(cre)Wrst/En1+ (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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