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Symbol
Name
ID
Aff3
AF4/FMR2 family, member 3
MGI:106927
Phenotype annotations related to skeleton
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
Availability Mouse Genotype
Aff3em1Andg/Aff3em1Andg
Aff3tm1a(EUCOMM)Wtsi/Aff3tm1a(EUCOMM)Wtsi
Aff3tm1a(EUCOMM)Wtsi/Aff3+

Contributing Projects:
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
The Jackson Laboratory