|
Symbol Name ID |
Wnt5a
wingless-type MMTV integration site family, member 5A MGI:98958 |
| Darker colors indicate more annotations |
| Human Phenotypes | Frontal bossing |
Micrognathia |
Retrognathia |
Malar flattening |
Macrocephaly |
Wide anterior fontanel |
Flat face |
Midface retrusion |
Long philtrum |
Thin upper lip vermilion |
Short lingual frenulum |
Gingival overgrowth |
Short hard palate |
High palate |
Narrow palate |
Bifid tongue |
Macroglossia |
Downturned corners of mouth |
Triangular mouth |
Delayed eruption of teeth |
Persistence of primary teeth |
Dental crowding |
Orofacial cleft |
Anteverted nares |
Depressed nasal bridge |
Wide nasal bridge |
Short nose |
Long eyelashes |
Long palpebral fissure |
Downslanted palpebral fissures |
Upslanted palpebral fissure |
Epicanthus |
| Disease(s) Associated with WNT5A | ||||||||||||||||||||||||||||||||
| autosomal dominant Robinow syndrome 1 |
| Mouse Phenotypes | abnormal craniofacial morphology |
short mandible |
micrognathia |
cleft upper lip |
cleft palate |
decreased tongue size |
short snout |
small ears |
|
| Availability | Mouse Genotype | ||||||||
| Wnt5ab2b3077.1Clo/Wnt5ab2b3077.1Clo | |||||||||
| Wnt5atm1Amc/Wnt5atm1Amc | |||||||||
| Wnt5atm1Amc/Wnt5atm1.1Krvl H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
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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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