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Symbol
Name
ID
Wnt5a
wingless-type MMTV integration site family, member 5A
MGI:98958
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Frontal bossing
Micrognathia
Retrognathia
Malar flattening
Macrocephaly
Wide anterior fontanel
Short neck
Short middle phalanx of the 5th finger
Duplication of the distal phalanx of hand
Broad thumb
Radial deviation of finger
Broad toe
Clinodactyly
Brachydactyly
Bifid distal phalanx of toe
Dislocated radial head
Short palm
Small hand
Limited elbow extension and supination
Mesomelia
Rhizomelia
Sacral dimple
Delayed skeletal maturation
Short long bone
Pectus excavatum
Disease(s) Associated with WNT5A
autosomal dominant Robinow syndrome 1

Mouse Phenotypes
short mandible
micrognathia
short humerus
short radius
short ulna
absent caudal vertebrae
decreased tracheal cartilage ring number
rib fusion
abnormal vertebrae morphology
small vertebrae
vertebral fusion
short vertebral column
delayed bone ossification
Availability Mouse Genotype
Wnt5ab2b3077.1Clo/Wnt5ab2b3077.1Clo
Wnt5atm1Amc/Wnt5atm1Amc

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
04/30/2024
MGI 6.23
The Jackson Laboratory