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Symbol Name ID |
Gpr161
G protein-coupled receptor 161 MGI:2685054 |
| Darker colors indicate more annotations |
| Human Phenotypes | Progressive macrocephaly |
Delayed cranial suture closure |
| Disease(s) Associated with GPR161 | ||
| medulloblastoma |
| Mouse Phenotypes | abnormal craniofacial morphology |
abnormal craniofacial bone morphology |
absent frontal bone |
small frontal bone |
small parietal bone |
abnormal mandible morphology |
small mandible |
mandible hypoplasia |
abnormal maxilla morphology |
small premaxilla |
small maxilla |
short maxilla |
enlarged nasal bone |
abnormal craniofacial development |
palatal shelves fail to meet at midline |
cleft hard palate |
nasal septum hypoplasia |
anotia |
small ears |
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| Availability | Mouse Genotype | |||||||||||||||||||
| Gpr161tm1Lex/Gpr161tm1Lex | ||||||||||||||||||||
| Gpr161tm1.2Smuk/Gpr161tm1.2Smuk 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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