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Symbol Name ID |
Memo1
mediator of cell motility 1 MGI:1924140 |
| Darker colors indicate more annotations |
| Mouse Phenotypes | abnormal craniofacial bone morphology |
wide coronal suture |
wide metopic suture |
abnormal cranium morphology |
basioccipital bone hypoplasia |
small basisphenoid bone |
basisphenoid bone hypoplasia |
abnormal cranial cartilage development |
abnormal neurocranium morphology |
presphenoid bone hypoplasia |
absent maxillary shelf |
maxillary shelf hypoplasia |
premaxilla hypoplasia |
maxilla hypoplasia |
absent palatine bone horizontal plate |
palatine bone horizontal plate hypoplasia |
domed cranium |
palate bone hypoplasia |
kyphosis |
abnormal bone ossification |
abnormal endochondral bone ossification |
failure of endochondral bone ossification |
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| Availability | Mouse Genotype | ||||||||||||||||||||||
| Memo1m1Will/Memo1m1Will | |||||||||||||||||||||||
| Memo1tm1b(EUCOMM)Wtsi/Memo1tm1b(EUCOMM)Wtsi | |||||||||||||||||||||||
| Memo1tm1.1Neh/Memo1tm1.1Neh Tg(CAG-cre/Esr1*)1Lbe/0 (conditional) |
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| H2az2Tg(Wnt1-cre)11Rth/H2az2+ Memo1tm1c(EUCOMM)Wtsi/Memo1tm1c(EUCOMM)Wtsi (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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