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Symbol Name ID |
Aff3
AF4/FMR2 family, member 3 MGI:106927 |
| Darker colors indicate more annotations |
| Human Phenotypes | Polydactyly |
Coxa valga |
Fibular hypoplasia |
Dislocated radial head |
Pes planus |
Hip dislocation |
Single transverse palmar crease |
Mesomelia |
| Disease(s) Associated with AFF3 | ||||||||
| KINSSHIP syndrome |
| Mouse Phenotypes | polydactyly |
abnormal fibula morphology |
abnormal tibia morphology |
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| Availability | Mouse Genotype | |||
| Aff3em1Andg/Aff3em1Andg | ||||
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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