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 04/23/2024 MGI 6.23 |
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