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Symbol Name ID |
Dym
dymeclin MGI:1918480 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Intellectual disability |
Waddling gait |
Severe global developmental delay |
| Disease(s) Associated with DYM | ||||
| Dyggve-Melchior-Clausen disease | ||||
| Smith-McCort dysplasia 1 |
| Mouse Phenotypes | decreased prepulse inhibition |
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| Availability | Mouse Genotype | |
| Dymem1(IMPC)Tcp/Dymem1(IMPC)Tcp | ||
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 05/14/2024 MGI 6.23 |
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