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Symbol Name ID |
Fras1
Fraser extracellular matrix complex subunit 1 MGI:2385368 |
| Darker colors indicate more annotations |
| Human Phenotypes | Corneal opacity |
Hypertelorism |
Anophthalmia |
Bilateral microphthalmos |
Blindness |
| Disease(s) Associated with FRAS1 | |||||
| Fraser syndrome 1 |
| Mouse Phenotypes | abnormal eye morphology |
microphthalmia |
narrow eye opening |
cryptophthalmos |
eyelids open at birth |
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| Availability | Mouse Genotype | |||||
| Fras1b2b3323Clo/Fras1b2b3323Clo | ||||||
| Fras1bfb/Fras1bfb | ||||||
| Fras1bl/Fras1bl | ||||||
| Fras1rdf/Fras1rdf | ||||||
| Fras1tm1Chpk/Fras1tm1Chpk | ||||||
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 04/09/2024 MGI 6.23 |
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