Symbol Name ID |
Wnt5a
wingless-type MMTV integration site family, member 5A MGI:98958 |
Darker colors indicate more annotations |
Human Phenotypes | 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 |
Disease(s) Associated with WNT5A | ||||||||||||||
autosomal dominant Robinow syndrome 1 |
Mouse Phenotypes | abnormal limb morphology |
abnormal autopod morphology |
decreased autopod size |
adactyly |
syndactyly |
short humerus |
short radius |
short ulna |
short limbs |
abnormal tail morphology |
absent caudal vertebrae |
short tail |
vestigial tail |
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Availability | Mouse Genotype | |||||||||||||
Wnt5ab2b3077.1Clo/Wnt5ab2b3077.1Clo | ||||||||||||||
Wnt5atm1Amc/Wnt5atm1Amc |
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 |
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