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Symbol Name ID |
Fbln5
fibulin 5 MGI:1346091 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Premature sagging cheeks |
| Disease(s) Associated with FBLN5 | ||
| autosomal recessive cutis laxa type IA |
| Mouse Phenotypes | abnormal craniofacial morphology |
short snout |
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| Availability | Mouse Genotype | ||
| Fbln5tm1Krc/Fbln5tm1Krc | |||
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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