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Symbol Name ID |
Sh3pxd2a
SH3 and PX domains 2A MGI:1298393 |
| Darker colors indicate more annotations |
| Mouse Phenotypes | persistent right 6th pharyngeal arch artery |
abnormal basioccipital bone morphology |
basisphenoid bone foramen |
absent hypoglossal canal |
absent styloid process |
fragmented Meckel's cartilage |
abnormal occipital bone morphology |
fusion of atlas and occipital bones |
abnormal hyoid bone body morphology |
abnormal oral cavity morphology |
cleft secondary palate |
abnormally deep median sulcus of tongue |
short tongue |
abnormal nasal cavity morphology |
abnormal nasal septum morphology |
abnormal vomeronasal organ morphology |
short snout |
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| Availability | Mouse Genotype | |||||||||||||||||
| Sh3pxd2aGt(OST445753)Lex/Sh3pxd2aGt(OST445753)Lex | ||||||||||||||||||
| Sh3pxd2atm1b(EUCOMM)Wtsi/Sh3pxd2atm1b(EUCOMM)Wtsi | ||||||||||||||||||
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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