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Symbol Name ID |
Alg9
ALG9 alpha-1,2-mannosyltransferase MGI:1924753 |
| Darker colors indicate more annotations |
| Human Phenotypes | Decreased fetal movement |
Inappropriate crying |
| Disease(s) Associated with ALG9 | ||
| congenital disorder of glycosylation Il |
| Mouse Phenotypes | abnormal vocalization |
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| Availability | Mouse Genotype | |
| Alg9em1(IMPC)J/Alg9+ | ||
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 05/21/2024 MGI 6.23 |
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