Symbol Name ID |
Dnm1l
dynamin 1-like MGI:1921256 |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Broad thumb |
Broad hallux |
Disease(s) Associated with DNM1L | |||
encephalopathy due to defective mitochondrial and peroxisomal fission 1 |
Mouse Phenotypes | abnormal posterior cranial fossa morphology |
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Availability | Mouse Genotype | |
Dnm1ltm1.1Miha/Dnm1ltm1.1Miha Tg(Nes-cre)1Kln/0 (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 08/02/2024 MGI 6.24 |
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