|
Symbol Name ID |
Flna
filamin, alpha MGI:95556 |
| Darker colors indicate more annotations |
| Human Phenotypes | Shallow orbits |
Cataract |
Iris coloboma |
Developmental glaucoma |
Optic nerve hypoplasia |
Hypertelorism |
Hypotelorism |
Proptosis |
Strabismus |
Hypermetropia |
Myopia |
Moderate myopia |
Visual field defect |
Glaucoma |
Ptosis |
Bilateral ptosis |
| Disease(s) Associated with FLNA | ||||||||||||||||
| craniosynostosis | ||||||||||||||||
| frontometaphyseal dysplasia 1 | ||||||||||||||||
| Melnick-Needles syndrome | ||||||||||||||||
| otopalatodigital syndrome type 1 | ||||||||||||||||
| otopalatodigital syndrome type 2 | ||||||||||||||||
| periventricular nodular heterotopia | ||||||||||||||||
| terminal osseous dysplasia | ||||||||||||||||
| X-linked cardiac valvular dysplasia | ||||||||||||||||
| X-linked chronic idiopathic intestinal pseudo-obstruction |
| Mouse Phenotypes | abnormal eye morphology |
irregularly shaped pupil |
mydriasis |
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| Availability | Mouse Genotype | |||
| FlnaDilp2/Flna+ | ||||
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 04/16/2024 MGI 6.23 |
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