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Symbol Name ID |
Fitm2
fat storage-inducing transmembrane protein 2 MGI:2444508 |
| Darker colors indicate more annotations |
| Human Phenotypes | Limb dystonia |
Developmental regression |
Global developmental delay |
Motor delay |
Delayed ability to walk |
Seizure |
| Disease(s) Associated with FITM2 | ||||||
| Siddiqi syndrome |
| Mouse Phenotypes | decreased prepulse inhibition |
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| Availability | Mouse Genotype | |
| Fitm2tm1.1(KOMP)Vlcg/Fitm2+ | ||
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 05/21/2024 MGI 6.23 |
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