Symbol Name ID |
Fbln5
fibulin 5 MGI:1346091 |
Darker colors indicate more annotations |
Human Phenotypes | Congenital diaphragmatic hernia |
Hypotonia |
Disease(s) Associated with FBLN5 | ||
autosomal recessive cutis laxa type IA |
Mouse Phenotypes | abnormal vascular smooth muscle physiology |
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Availability | Mouse Genotype | |
Fbln5tm1Eno/Fbln5tm1Eno |
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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