Symbol Name ID |
Aff3
AF4/FMR2 family, member 3 MGI:106927 |
Darker colors indicate more annotations |
Human Phenotypes | Micrognathia |
Mandibular prognathia |
Dandy-Walker malformation |
Enlarged cisterna magna |
Microcephaly |
Primary microcephaly |
Short neck |
Polydactyly |
Coxa valga |
Fibular hypoplasia |
Dislocated radial head |
Hip dislocation |
Mesomelia |
Sacral dimple |
Supernumerary ribs |
Cervical ribs |
Scoliosis |
Osteopenia |
Disease(s) Associated with AFF3 | ||||||||||||||||||
KINSSHIP syndrome |
Mouse Phenotypes | abnormal tooth morphology |
abnormal incisor morphology |
abnormal fibula morphology |
abnormal tibia morphology |
decreased length of long bones |
abnormal pelvic girdle bone morphology |
abnormal vertebral arch morphology |
fusion of vertebral arches |
vertebral transformation |
delayed bone ossification |
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Availability | Mouse Genotype | ||||||||||
Aff3em1Andg/Aff3em1Andg | |||||||||||
Aff3tm1a(EUCOMM)Wtsi/Aff3tm1a(EUCOMM)Wtsi | |||||||||||
Aff3tm1a(EUCOMM)Wtsi/Aff3+ |
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 08/02/2024 MGI 6.24 |
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