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Symbol Name ID |
Morc2a
microrchidia 2A MGI:1921772 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Abnormal facial shape |
Tongue atrophy |
| Disease(s) Associated with MORC2 | |||
| Charcot-Marie-Tooth disease axonal type 2Z |
| Mouse Phenotypes | basisphenoid bone foramen |
abnormal Meckel's cartilage morphology |
fragmented Meckel's cartilage |
abnormal occipital bone morphology |
absent occipital bone |
abnormal sphenoid bone morphology |
absent neurocranium |
abnormal hyoid bone body morphology |
abnormal jaw morphology |
abnormal incisor morphology |
absent upper incisors |
domed cranium |
abnormal middle ear ossicle morphology |
abnormal stapes morphology |
abnormal masticatory muscle morphology |
tongue hypoplasia |
short tongue |
abnormal nasal cavity morphology |
abnormal nasal septum morphology |
abnormal vomeronasal organ morphology |
facial cleft |
abnormal external auditory canal morphology |
absent external auditory canal |
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| Availability | Mouse Genotype | |||||||||||||||||||||||
| Morc2aem1(IMPC)Wtsi/Morc2aem1(IMPC)Wtsi | ||||||||||||||||||||||||
| Morc2atm1.1Pngr/Morc2atm1.1Pngr Tg(Nes-cre)1Kln/0 (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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