|
Symbol Name ID |
Copb2
COPI coat complex subunit beta 2 MGI:1354962 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormality of body height |
Decreased body weight |
Failure to thrive in infancy |
| Disease(s) Associated with COPB2 | |||
| primary autosomal recessive microcephaly 19 |
| Mouse Phenotypes | decreased birth body size |
increased lean body mass |
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| Availability | Mouse Genotype | ||
| Copb2em1(IMPC)Bay/Copb2+ | |||
| Copb2em1Rstot/Copb2em2Rstot | |||
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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