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Symbol Name ID |
Rnf2
ring finger protein 2 MGI:1101759 |
| Darker colors indicate more annotations |
| Human Phenotypes | Primary microcephaly |
Intellectual disability, severe |
Hyperreflexia |
Severe global developmental delay |
Seizure |
| Disease(s) Associated with RNF2 | |||||
| Luo-Schoch-Yamamoto syndrome |
| Mouse Phenotypes | abnormal neuron differentiation |
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| Availability | Mouse Genotype | |
| Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+ Rnf2tm1Mvi/Rnf2tm1Mvi (conditional) |
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| Rnf2tm1Mvi/Rnf2tm1Mvi Tg(Nes-cre/ERT2)5-1Imayo/0 (conditional) |
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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 04/23/2024 MGI 6.23 |
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